Pharmacy Jobs in Delhi

Why This Role MattersThe Project Technical Staff-I role supports research and technical activities in a healthcare and scientific environment. This position assists research teams with documentation, data management, and technical support, helping ensure smooth execution of research projects and administrative tasks.Job DescriptionThe organization is seeking a Project Technical Staff-I to assist in research and project-related activities. The role involves supporting technical tasks, maintaining records, and assisting research teams in managing project documentation and data.Number of Vacancies: 1The Project Technical Staff-I will:• Support research and project-related technical activities• Maintain project documentation and records• Assist in data entry and report preparation• Support administrative and research coordination tasks• Work with research teams to ensure smooth project operationsKey Features of the Role• Opportunity to work in a reputed medical research institution• Exposure to research project management and documentation• Experience in data management and technical support• Collaboration with healthcare and research professionalsResponsibilities• Assist in maintaining research documentation and records• Perform data entry and documentation using MS Word and Excel• Support research teams with project-related tasks• Maintain organized records of project activities• Assist with administrative coordination related to research projectsRequired QualificationsEducational Requirements:• 10th / 12th / Diploma / D.Pharm from a recognized institutionExperience and Skills:• Proficiency in MS Word and MS Excel• Previous research experience will be considered desirable• Basic documentation and data management skills• Ability to work in a team and support research activitiesAge Eligibility• Minimum age: 18 years• Maximum age: 28 yearsSalary Insights• Salary will be provided as per project and institutional guidelinesOrganization OverviewThe All India Institute of Medical Sciences (AIIMS), Delhi is one of India’s premier medical institutions known for excellence in medical education, healthcare services, and biomedical research.FAQs• What does a Project Technical Staff-I do?The role involves assisting research teams with documentation, data entry, and technical support for project activities.• What qualifications are required?Candidates with 10th, 12th, Diploma, or D.Pharm qualifications are eligible.• Is research experience required?Research experience is not mandatory but will be considered desirable.• What computer skills are needed?Basic proficiency in MS Word and MS Excel is preferred.Application Tips• Highlight computer skills such as MS Word and Excel• Mention any research or laboratory experience if available• Include details of diploma or pharmacy qualifications• Ensure educational certificates are ready for verificationClosing Date: 13-03-2026Official Notification Click Here

Why This Role MattersThis role offers an opportunity to work as a Pharmacist in a regulated healthcare environment where accurate dispensing, compliance with pharmaceutical regulations, and patient safety are key priorities. The position enables professionals to apply their pharmacy knowledge while contributing to safe medication practices.Job DescriptionWe are seeking a qualified Pharmacist to ensure proper dispensing of medications and adherence to pharmacy regulations. The role involves maintaining pharmacy standards, supporting patient care, and ensuring compliance with statutory requirements.Number of Vacancies: 1The Pharmacist will:• Dispense medicines accurately according to prescriptions• Ensure compliance with pharmaceutical regulations and safety standards• Maintain pharmacy records and documentation• Provide guidance on medication usage and storage• Monitor drug inventory and maintain stock levels• Follow professional and ethical pharmacy practicesKey Features of the Role• Opportunity to work in a regulated healthcare environment• Involvement in dispensing and medication safety practices• Exposure to pharmacy compliance and documentation processes• Professional development in clinical and regulatory pharmacy workResponsibilities• Dispense prescribed medicines accurately• Maintain prescription records and pharmacy documentation• Ensure safe storage and handling of medicines• Monitor inventory and manage stock levels• Follow regulatory and safety standards in pharmacy operationsRequired QualificationsEducational Requirements:• Bachelor Degree in Pharmacy (B. Pharm) from a recognized university or equivalentProfessional Requirements:• Registered as a Pharmacist under the Pharmacy Act, 1948• Selected candidate must register with the Delhi Pharmacy Council within six months of joiningAge Eligibility• Maximum age: 27 yearsSalary Insights• Salary will be provided as per organizational norms and applicable policiesOrganization OverviewTelecommunications Consultants India Limited (TCIL) is a Government of India enterprise providing engineering and consultancy services in telecommunications and IT sectors. The organization supports various national and international projects while maintaining high professional standards.FAQs• What does a Pharmacist do in this role?Responsible for dispensing medicines, maintaining pharmacy records, and ensuring compliance with pharmacy regulations.• Is registration required for this position?Yes. Candidates must be registered under the Pharmacy Act, 1948 and register with the Delhi Pharmacy Council within six months of joining.• What qualifications are required?A Bachelor of Pharmacy (B. Pharm) degree from a recognized university.• Is experience required?Experience may be preferred but eligibility primarily depends on the required educational qualification and registration.Application Tips• Highlight your B. Pharm qualification clearly in the resume• Include pharmacy registration details if available• Emphasize knowledge of pharmacy regulations and dispensing practices• Ensure all academic and registration documents are ready for verificationClosing Date: 13-03-2026Official Notification Click Here

Why This Role MattersThis position provides an opportunity to contribute to high-impact research in the life sciences at a premier medical institution. As a Senior Research Fellow at AIIMS Delhi, you will engage in advanced molecular and laboratory techniques, support ongoing research projects, and contribute to scientific discovery.The role allows professional growth, hands-on experience with cutting-edge research methodologies, and collaboration with leading researchers in the field.Job DescriptionWe are seeking a Senior Research Fellow for AIIMS Delhi. This role involves conducting research using molecular techniques, handling laboratory animals, performing RNA/DNA isolation, ELISA, and other advanced laboratory procedures.The Senior Research Fellow will:• Conduct experiments using molecular biology techniques such as RT-PCR• Handle laboratory animals in accordance with ethical standards• Perform RNA and DNA isolation, ELISA, and related assays• Participate in research project planning, execution, and documentation• Contribute to data analysis, interpretation, and reporting of research findings• Collaborate with principal investigators and research teams• Ensure compliance with laboratory safety and regulatory guidelinesKey Features of the Role• Work at AIIMS Delhi, a leading medical research institution• Exposure to advanced molecular biology techniques and research methodologies• Opportunity to contribute to high-impact scientific research• Hands-on experience with animal handling and laboratory protocols• Collaboration with experienced research professionals• Professional development in experimental design, data analysis, and reportingResponsibilities• Execute research experiments using molecular biology and biochemical techniques• Isolate RNA and DNA, perform ELISA, and related laboratory assays• Handle laboratory animals ethically and safely• Maintain accurate records of experiments and research data• Support preparation of reports, presentations, and publications• Participate in project meetings and provide updates on research progress• Follow institutional and regulatory guidelines for laboratory safety and ethicsRequired QualificationsEducational Requirements:• Post-graduate degree in Life Sciences, M.Sc, or M. Pharm• Selection preferably through:• National Eligibility Test (CSIR-UGC NET including lectureship/Assistant Professorship) and GATE/GPAT, OR• National level examination conducted by Central Government Departments/Institutions (DST, DBT, DAE, DOS, DRDO, MHRD, ICAR, ICMR, IITs, IISc, IISER)Experience & Skills:• Minimum 2 years of research experience• Proficiency in molecular techniques, RT-PCR, ELISA, RNA/DNA isolation• Experience with animal handling• Strong analytical and data documentation skills• Ability to work collaboratively within a research teamAge Eligibility• Minimum age: 18 years• Maximum age: 35 yearsSalary Insights• As per AIIMS Delhi fellowship guidelines• Competitive remuneration with exposure to advanced research opportunitiesCompany OverviewAIIMS Delhi is a premier medical and research institution in India, known for excellence in healthcare, education, and scientific research. The institution fosters innovation, multidisciplinary collaboration, and professional development for researchers and medical professionals.FAQs• What does a Senior Research Fellow do in this role?Conducts molecular biology experiments, handles laboratory animals, isolates RNA/DNA, performs ELISA, analyzes data, and contributes to research reporting.• Is prior research experience required?Yes. Minimum 2 years of relevant research experience is required.• What skills are important for this position?Molecular biology techniques, animal handling, RNA/DNA isolation, ELISA, data analysis, and teamwork.• What is the age limit for applicants?Minimum 18 years and maximum 35 years.Application Tips• Highlight post-graduate qualifications (M.Sc, M. Pharm, or Life Sciences)• Include experience with molecular biology techniques and laboratory research• Emphasize animal handling and data analysis skills• Showcase prior research publications or project contributions if applicable• Ensure eligibility criteria (NET, GATE/GPAT, or national-level selection) are clearly mentionedClosing Date: 13-03-2026Official Notification Click Here

Why This Role MattersSenior Pharmacists play a critical role in ensuring safe medication dispensing, effective pharmacy operations, and high-quality patient service in retail pharmacy settings. With increasing demand for accessible healthcare services, experienced pharmacists help maintain professional standards, guide junior staff, and ensure compliance with pharmacy regulations.This role not only focuses on dispensing medicines but also on improving patient counseling, maintaining inventory accuracy, and supporting smooth pharmacy operations. By supervising pharmacy teams and ensuring quality service, Senior Pharmacists contribute to patient safety and the overall efficiency of retail pharmacy outlets.Job DescriptionZeelab Pharmacy is hiring a Senior Pharmacist for its North Delhi retail pharmacy location. This position is designed for experienced pharmacy professionals who have a strong understanding of retail pharmacy operations, medication dispensing, and customer interaction.The Senior Pharmacist will oversee daily pharmacy activities, ensure accurate dispensing of medicines, guide pharmacy staff, and provide professional patient counseling. The role requires operational expertise, strong communication skills, and the ability to maintain high service standards within the pharmacy.Key Features of the Role:• Leadership role within a retail pharmacy environment• Opportunity to manage pharmacy operations and guide pharmacy teams• Direct interaction with patients and healthcare customers• Involvement in medicine dispensing, counseling, and inventory management• Opportunity to work with a growing pharmacy retail network• Exposure to operational management and customer service excellenceResponsibilities• Oversee day-to-day operations of the pharmacy outlet• Dispense prescription and over-the-counter medications accurately• Ensure compliance with pharmacy regulations and company policies• Provide patient counseling on medication usage, dosage, and safety• Monitor pharmacy inventory levels and ensure proper stock availability• Coordinate with procurement teams for timely medicine supply• Guide and supervise pharmacy assistants and junior pharmacists• Maintain proper documentation for prescriptions and pharmacy records• Ensure proper storage conditions for medicines and pharmaceutical products• Address customer queries and provide professional healthcare guidance• Support sales targets while maintaining ethical pharmacy practicesRequired QualificationsEducational Requirements:• Bachelor of Pharmacy (B.Pharm) or Diploma in Pharmacy (D.Pharm)• Registered Pharmacist license as per regulatory requirementsExperience and Skills:• Minimum 3–4 years of experience in retail pharmacy operations• Strong knowledge of medication dispensing and pharmaceutical products• Experience in managing pharmacy inventory and stock control• Good communication and customer handling skills• Ability to supervise pharmacy staff and manage workflow efficiently• Strong attention to detail and commitment to patient safety• Familiarity with pharmacy management systems and billing softwareSalary Insights:• Additional incentives or performance-based benefits may be offeredCompany OverviewZeelab Pharmacy is a rapidly expanding retail pharmacy chain focused on providing affordable medicines and healthcare products across India. The company is committed to improving accessibility to quality pharmaceutical care through its network of pharmacy outlets.With a strong focus on customer service, product availability, and healthcare support, Zeelab Pharmacy aims to create reliable pharmacy services for communities while maintaining professional pharmacy standards.FAQsWhat does a Senior Pharmacist do in retail pharmacy?A Senior Pharmacist manages pharmacy operations, supervises staff, dispenses medications, provides patient counseling, and ensures regulatory compliance.Is prior retail pharmacy experience required?Yes. Candidates are expected to have at least 3–4 years of experience working in a retail pharmacy environment.Is pharmacist registration required for this role?Yes. Candidates must hold a valid pharmacist registration as per regulatory guidelines.What skills are important for this position?Strong medication knowledge, customer service skills, inventory management, and pharmacy operations experience are essential.Application Tips• Highlight your experience in retail pharmacy operations• Mention pharmacist registration and relevant pharmacy qualifications• Include examples of managing pharmacy inventory or supervising staff• Emphasize customer service and patient counseling experience• Demonstrate knowledge of pharmacy regulations and dispensing practices.

Why This Role MattersThe Associate – Healthcare & Lifesciences plays a strategic role in supporting data-driven decision-making for global healthcare clients. In today’s competitive and innovation-driven environment, pharmaceutical, biotech, MedTech, digital health, payer, and provider organizations require sharp analytical insight to navigate market expansion, portfolio prioritization, cost optimization, mergers and acquisitions, and growth strategy. This role directly contributes to solving such high-impact business challenges.Working within Bain & Company, one of the world’s leading consulting firms, offers exposure to global case teams and structured consulting methodologies. The Associate contributes to hypothesis-driven analysis, financial modeling, market assessments, and executive-ready deliverables that influence client decisions at the leadership level.This position is particularly valuable for professionals seeking long-term careers in strategy consulting, healthcare analytics, or corporate strategy. It strengthens structured thinking, quantitative rigor, and business storytelling—core skills required for senior consulting and leadership roles. The role also provides cross-regional exposure, supporting teams across EMEA, Americas, and APAC, making it an excellent platform for international professional development.Job DescriptionThe Associate – Healthcare & Lifesciences will lead defined analytical workstreams under supervision and collaborate closely with global consulting teams. The role involves conducting detailed industry research, building financial and strategic models, synthesizing complex data, and preparing high-impact client presentations.Associates are expected to apply Bain’s answer-first approach, where hypotheses are structured early and validated through targeted analysis. The role demands intellectual curiosity, business judgment, and the ability to transform data into actionable insights. Deliverables must meet global consulting standards in clarity, accuracy, and executive presentation quality.The position is based in India within the Bain Capability Network (BCN), which serves as an analytics and research backbone for global Bain case teams. Associates contribute meaningfully to client-facing engagements while developing deep sector knowledge in healthcare and lifesciences.Key Features of the Role:• Exposure to global healthcare consulting engagements• Structured problem-solving using hypothesis-driven methodologies• Involvement in financial modeling and market landscape assessments• Development of executive-ready PowerPoint presentations• Collaboration with international teams across multiple time zones• Opportunity to specialize in pharmaceuticals, biotech, MedTech, digital health, or payer/provider segments• Strong career pathway into consulting leadership rolesResponsibilities• Lead assigned analytical workstreams with supervisor guidance• Conduct primary and secondary research across healthcare and lifesciences sectors• Perform competitive benchmarking and market sizing analysis• Develop financial models, forecasting tools, and valuation frameworks• Analyze pharma and biotech company performance metrics• Generate actionable insights from large datasets• Develop structured hypotheses and validate through quantitative analysis• Create clear, compelling, and structured client presentations in PowerPoint• Utilize databases such as CapitalIQ, Factiva, D&B, and similar platforms• Support due diligence, growth strategy, and portfolio optimization projects• Communicate findings effectively to consulting team members• Ensure data accuracy, logical consistency, and high-quality outputsRequired QualificationsCandidates must demonstrate strong analytical capability and structured thinking ability. The role requires comfort with numbers, financial interpretation, and market data. Attention to detail, intellectual rigor, and the ability to work under tight deadlines are critical for success.Strong written and verbal communication skills are essential, as the Associate must present findings in a clear and concise manner. Proficiency in Excel for financial modeling and PowerPoint for executive presentations is mandatory. Exposure to analytical tools such as Tableau, Alteryx, Python, or R is considered an advantage.Educational Requirements:• Undergraduate degree with a minimum of 2 years of relevant experienceOR• Postgraduate degree with 0–1 year of relevant experienceCandidates from healthcare, life sciences, pharmacy, biotechnology, economics, engineering, or business backgrounds are preferred, though strong analytical professionals from other disciplines may also be considered.Experience and Skills:• Prior experience in consulting, analytics, equity research, healthcare strategy, or market research is advantageous• Strong quantitative and financial analysis skills• Experience working with global databases such as Thomson Reuters or CapitalIQ (preferred)• Advanced Excel capabilities including pivot tables, financial modeling, and data structuring• Strong storytelling and slide structuring skills in PowerPoint• Ability to work collaboratively in fast-paced team environments• Strong time management and multitasking ability• Intellectual curiosity and proactive problem-solving mindsetSalary InsightsFor Associate-level roles in management consulting analytics in India, the estimated compensation range is ₹12,00,000 – ₹18,00,000 per annum (CTC). Final salary may vary based on candidate experience, educational background, performance in the interview process, and internal compensation banding policies.In addition to fixed compensation, employees may receive performance-linked bonuses and access to global learning resources, structured training programs, and career mobility opportunities within the organization.Company OverviewBain & Company is a globally recognized management consulting firm operating in 61 offices across 39 countries. The firm advises leading businesses, private equity firms, and public institutions on strategy, operations, mergers and acquisitions, digital transformation, and organizational effectiveness.In India, the Bain Capability Network (BCN) functions as a high-impact analytics and research hub supporting global case teams. The network plays a vital role in delivering data-backed insights, structured analysis, and strategic recommendations to clients worldwide. Bain is known for its collaborative culture, rigorous problem-solving frameworks, and strong emphasis on professional growth and mentorship.FAQsIs healthcare experience mandatory for this role?Healthcare background is preferred but not mandatory. Strong analytical and consulting capabilities are prioritized.Is prior consulting experience required?Not mandatory, but experience in consulting, analytics, or financial research provides a competitive advantage.What tools should candidates be proficient in?Strong command over MS Excel and PowerPoint is essential. Familiarity with financial databases and analytical tools is a plus.What career growth can be expected?The role provides a pathway to Senior Associate, Consultant, and leadership roles within strategy consulting or corporate strategy functions.Does the role involve global exposure?Yes, Associates support consulting teams across EMEA, Americas, and APAC regions.Application Tips• Highlight structured problem-solving examples in your resume.• Demonstrate financial modeling and data analysis expertise.• Showcase PowerPoint presentation samples if possible.• Emphasize healthcare or lifesciences exposure if applicable.• Prepare to discuss case-based problem-solving during interviews.• Demonstrate clarity of thought and hypothesis-driven thinking in discussions.

Why This Role MattersThe Pharmacovigilance Intern role at CliniResource provides an essential entry point into the highly regulated and critical field of drug safety and pharmacovigilance. Pharmacovigilance plays a vital role in protecting patient safety by monitoring, assessing, and reporting adverse drug reactions in compliance with global regulatory frameworks.This internship offers fresh graduates structured exposure to real-world pharmacovigilance workflows followed by pharmaceutical companies and Contract Research Organizations (CROs). By contributing to adverse event case processing, safety documentation, and regulatory compliance activities, interns gain foundational experience that directly supports public health and regulatory transparency.For candidates seeking pharmacovigilance internship jobs in Delhi/NCR, this opportunity strengthens industry readiness and builds the professional discipline required in global drug safety operations.Job DescriptionCliniResource is offering an office-based Pharmacovigilance Internship for fresh M.Pharm, Pharm.D, and BDS graduates located in New Delhi/NCR. This role is designed to provide structured, hands-on training in pharmacovigilance case processing, adverse event reporting, and regulatory documentation practices.The selected interns will work closely with safety and regulatory teams to process Adverse Event (AE) and Serious Adverse Event (SAE) reports, assist in Individual Case Safety Report (ICSR) documentation, maintain safety databases, and support compliance activities aligned with ICH and global pharmacovigilance guidelines.This internship focuses on building core competencies required for entry-level drug safety and pharmacovigilance roles within pharmaceutical companies and CRO environments.Key Features of the Role• Structured hands-on training in pharmacovigilance operations• Exposure to AE and SAE case processing workflows• Practical learning of ICSR documentation procedures• Compliance alignment with ICH and global regulatory standards• Real-time safety database management experience• Office-based professional learning environment• Direct interaction with pharmacovigilance and regulatory professionals• Foundational training for long-term drug safety careersResponsibilities Required• Process and review Adverse Event (AE) reports• Assist in handling Serious Adverse Event (SAE) documentation• Support preparation and review of Individual Case Safety Reports (ICSRs)• Maintain accurate safety database entries and documentation records• Assist in aggregate safety data review activities• Ensure compliance with ICH guidelines and global pharmacovigilance standards• Coordinate with internal safety and regulatory teams for case follow-up• Support documentation accuracy and case tracking processes• Maintain confidentiality and data integrity across safety workflows• Participate in internal training and quality review sessionsQualifications• M.Pharm (Pharmacology or Pharmaceutics preferred)• Pharm.D• BDSEducational Requirements• Completed postgraduate or professional degree in Pharmacy or Dentistry• Academic understanding of pharmacology, drug safety, and adverse event monitoringExperience and Skills• Fresh graduates are eligible• Strong conceptual understanding of pharmacovigilance principles• Basic knowledge of ICH guidelines and global drug safety regulations• Good written and verbal communication skills• Strong attention to detail and documentation accuracy• Ability to understand and interpret medical terminology• Structured and process-oriented working style• Basic computer proficiency for database documentation• Willingness to learn regulated safety workflows• Ability to work effectively in an office-based professional settingSalary Insights• Estimated stipend: ₹12,000 – ₹18,000 per month• Compensation aligned with industry standards for pharmacovigilance interns in Delhi/NCR• Internship provides high-value industry exposure beyond monetary compensation• Strong return on investment in terms of long-term career growth potentialCompany OverviewCliniResource operates within the pharmaceutical and clinical research domain, supporting pharmacovigilance and drug safety operations. The organization focuses on providing structured training and operational exposure to fresh graduates entering regulated healthcare environments.Through practical safety case processing, compliance documentation, and regulatory alignment, CliniResource enables early-career professionals to develop strong foundations in pharmacovigilance operations. The company emphasizes process discipline, regulatory accuracy, and professional development within a structured office-based environment.FAQs• Q: Is this internship remote?A: No. This is an office-based internship located in New Delhi/NCR.• Q: Are freshers eligible?A: Yes. Fresh M.Pharm, Pharm.D, and BDS graduates are encouraged to apply.• Q: Is prior pharmacovigilance experience required?A: No prior industry experience is mandatory, but basic conceptual understanding is expected.• Q: Will interns receive hands-on ICSR exposure?A: Yes. Interns will assist in ICSR documentation and safety case processing workflows.• Q: What career roles can this internship lead to?A: This internship builds a foundation for roles such as Drug Safety Associate, Pharmacovigilance Executive, Safety Scientist, or Clinical Research professional.• Q: Are candidates outside Delhi/NCR eligible?A: No. Only candidates residing in Delhi/NCR are eligible.Application Tips• Highlight academic projects related to pharmacovigilance or drug safety• Mention coursework in pharmacology, clinical research, or regulatory affairs• Demonstrate understanding of AE, SAE, and ICSR concepts• Emphasize documentation accuracy and attention to detail• Showcase strong communication skills in your resume• Prepare to discuss basic ICH guidelines during interviews• Express willingness to learn structured, regulated workflows

Why This Role MattersIn the pharmaceutical industry, regulatory compliance is critical to ensure that products are safe, effective, and legally marketable across global markets. Regulatory Affairs Managers act as the bridge between development teams and regulatory authorities, ensuring that all documentation, approvals, and submissions adhere to national and international standards. Non-compliance or delayed submissions can result in product launch delays, regulatory actions, or reputational risk.This role is pivotal in maintaining compliance throughout a product’s lifecycle from development and clinical trials to post-marketing surveillance—ensuring timely approvals and alignment with evolving regulatory guidelines. By managing submissions, approvals, and documentation, the Regulatory Affairs Manager supports product quality, market access, and overall business success.Job DescriptionWe are seeking a detail-oriented and highly skilled Regulatory Affairs Manager – Pharmaceuticals to oversee regulatory documentation, submissions, and compliance activities. The role focuses on preparing high-quality regulatory dossiers, liaising with health authorities, and ensuring that pharmaceutical products meet global regulatory standards. The candidate will collaborate with cross-functional teams such as R&D, QA/QC, Medical Affairs, and Manufacturing to ensure regulatory readiness and compliance across all stages of the product lifecycle.This is a full-time position based in New Delhi, India, reporting to the Managing Director/Manager Operations.Key Features of the Role• Full ownership of regulatory submissions and approvals• Cross-functional collaboration across R&D, QA/QC, and Manufacturing• Exposure to global regulatory frameworks including FDA, EMA, ICH, CDSCO• Strategic involvement in regulatory risk assessments and lifecycle management• Oversight of labeling, packaging, and promotional compliance• Active role in clinical trial applications and post-marketing surveillanceResponsibilities• Approve labels, packaging, and promotional materials (leaflets, websites, social media) for compliance under FSSR and other export market rules as per applicable guidelines• Summarize scientific and technical data for regulatory submissions• Prepare, compile, and submit regulatory dossiers for new product approvals, renewals, and variations• Ensure timely submissions to regulatory agencies• Manage communication and correspondence with health authorities• Track and interpret changes in pharmaceutical regulations and provide guidance to internal stakeholders• Review and approve product labeling, packaging, and promotional materials for regulatory compliance• Support clinical trials by submitting and maintaining INDs or clinical trial applications (CTA)• Maintain regulatory databases and documentation for inspections and audits• Liaise with cross-functional teams (R&D, QA/QC, Medical Affairs, Manufacturing) to ensure compliance and regulatory readiness• Contribute to regulatory strategy and risk assessments during drug development and post-marketing phasesRequired Qualifications• Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or related field• 5–8 years of experience in pharmaceutical regulatory affairs• Strong knowledge of global regulatory requirements (FDA, EMA, ICH, CDSCO, etc.)• Attention to detail, critical thinking, and organizational skills• Excellent written and verbal communication skillsPreferred Qualifications• Regulatory Affairs Certification (RAC) or equivalent is a plus• Familiarity with global submission platforms (e.g., ESG, CESP, EU Portal)• Experience in new drug applications (NDA), abbreviated NDAs (ANDA), and post-marketing surveillanceEducational Requirements• Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline• Candidates with a strong academic foundation in pharmaceutical sciences and interest in regulatory affairs are encouraged to applyExperience and Skills• 5–8 years of relevant experience in pharmaceutical regulatory affairs• Experience in preparing regulatory dossiers, INDs, CTAs, NDAs, and ANDAs• Exposure to global regulatory submission platforms• Strong knowledge of compliance standards across multiple jurisdictions• Ability to manage multiple submissions and timelines effectively• Excellent documentation, analytical, and problem-solving skills• Strong stakeholder management and cross-functional coordination abilities• Proactive approach to monitoring regulatory changes and implementing updatesSalary Insights• Compensation: ₹30,000 – ₹50,000 per month• Salary aligned with industry standards for Regulatory Affairs Managers in India• Additional benefits include cell phone reimbursement, health benefits, and performance incentivesCompany OverviewThe organization is a pharmaceutical company committed to innovation, compliance, and global product accessibility. With a strong focus on regulatory excellence, the company ensures that all products meet national and international standards, supporting patient safety and business growth. The company culture emphasizes teamwork, professional development, and adherence to ethical and regulatory practices.FAQsIs prior experience in regulatory affairs mandatory?Yes, 5–8 years of experience in pharmaceutical regulatory affairs is required.Does this role involve cross-functional coordination?Yes, the position requires regular collaboration with R&D, QA/QC, Medical Affairs, and Manufacturing teams.Are global regulatory frameworks relevant?Yes, strong knowledge of FDA, EMA, ICH, and CDSCO regulations is essential.Will the role handle clinical trial applications?Yes, the candidate will support IND and CTA submissions for clinical trials.Is approval of labeling and promotional material included?Yes, reviewing and approving product labeling, packaging, and promotional content is part of the role.Application Tips• Highlight regulatory submission experience (NDAs, ANDAs, INDs, CTAs)• Emphasize global regulatory knowledge and compliance exposure• Mention experience with labeling, packaging, and promotional approvals• Showcase cross-functional collaboration and communication skills• Provide examples of managing submission timelines and inspections

Why This Role MattersPharmacovigilance leaders play a vital role in ensuring drug safety compliance, signal evaluation, and regulatory excellence. This position supports strategic PV operations while mentoring teams and maintaining high-quality safety standards.Job DescriptionCliniResource is hiring a Pharmacovigilance Team Lead / SME / Associate Manager for its New Delhi/NCR office. This is a full-time, office-based leadership opportunity for professionals with 3–5 years of comprehensive pharmacovigilance experience. Candidates with only ICSR processing experience are not eligible.Key Features of the Role:• Location: New Delhi / NCR (Office-based only)• Experience: 3–5 years• Employment Type: Full-time• Leadership opportunity• Open to professionals returning after a career break• Not eligible: Candidates with only ICSR experience or those outside Delhi/NCRResponsibilities• Oversee end-to-end pharmacovigilance activities• Lead and mentor PV team members• Ensure regulatory compliance with global PV guidelines• Review safety cases, aggregate reports, and signal data• Coordinate with cross-functional stakeholders• Maintain SOP adherence and quality standards• Support audits and regulatory inspectionsRequired Qualifications• M.Pharm• Pharm.D• BDS• Minimum 3 years of comprehensive pharmacovigilance experienceExperience and Skills:• Strong understanding of global PV regulations (ICH, FDA, EMA)• Experience beyond basic ICSR processing• Leadership and mentoring capability• Analytical and problem-solving skills• Excellent communication and documentation skills• Ability to manage team performance and deadlinesSalary InsightsSalary not disclosed (expected competitive package aligned with experience and leadership role).FAQsQ1 Is this a remote role?No, this is strictly office-based in Delhi/NCR.Q2 Are candidates with only ICSR experience eligible?No, comprehensive PV experience beyond ICSR is required.Q3 Is this role suitable for someone returning after a career break?Yes, experienced professionals making a comeback are encouraged to apply.Q4 What qualifications are required?M.Pharm, Pharm.D, or BDS.Q5 Is leadership experience required?Yes, as this is a Team Lead/SME/Associate Manager level role.Application Tips• Highlight leadership or mentoring experience• Specify aggregate reporting, signal management, or risk management exposure• Mention regulatory guideline familiarity• Confirm Delhi/NCR availability• Clearly state total pharmacovigilance experience (3–5 years)

Roles & Responsibilities• Promote company products to doctors, physicians, and healthcare professionals• Arrange regular meetings with doctors, pharmacists, and hospital staff• Explain product composition, benefits, usage, dosage, and competitive advantages• Achieve monthly and quarterly sales targets as per territory plan• Maintain daily call reports, doctor visit records, and sales data• Monitor competitor activities, schemes, and market trends• Ensure product availability at pharmacies and stockists• Coordinate with production and supply teams for stock planning and forecastingMarket Analysis• Map total doctors in assigned territory and analyze prescribing patterns• Identify which doctor prescribes which brand• Track strong competitor companies in the territory• Assess high-demand medicines and growth segments• Collect information on competitor schemes, discounts, and promotional strategiesSales Training & Development• Learn detailed product composition and therapeutic benefits• Understand diseases, indications, and treatment guidelines• Develop effective product detailing skills for doctors• Handle doctor objections confidently and professionally• Conduct competitor product comparisons• Maintain accurate reporting and territory managementKOL Engagement• Build strong relationships with senior doctors• Engage specialist consultants and department heads• Interact with medical professors and key hospital decision-makersQualification• B. Pharm (Bachelor of Pharmacy)• M. Pharm (Master of Pharmacy)• B.Sc (Bachelor of Science)• MBA in PharmaceuticalsExperience• 0–3 years of experience in pharmaceutical sales (preferred)Skills • Strong communication and presentation skills• Good knowledge of pharmaceutical products and disease areas• Sales and negotiation abilities• Analytical skills for market assessment• Relationship-building and networking capability• Time management and territory planning skills• Proficiency in MS Office and reporting toolsAbout the CompanyMaximon Wellness is a growing pharmaceutical company focused on delivering quality healthcare products and building strong partnerships with medical professionals across its operational territories.

Roles & Responsibilities• Accurately dispense medications as per valid prescriptions• Review prescriptions for dosage accuracy, interactions, and contraindications• Ensure proper storage and handling of medicines as per hospital and statutory guidelines• Maintain pharmacy inventory and monitor stock levels• Counsel patients on medication usage, dosage, side effects, and precautions• Maintain dispensing records and ensure compliance with regulatory requirements• Coordinate with doctors and nursing staff for effective medication managementQualification• B. Pharm (Bachelor of Pharmacy)• D. Pharm (Diploma in Pharmacy)• Valid Delhi Pharmacy Council (DPC) Registration (DPS mandatory)Experience• 1–3 years of relevant hospital or retail pharmacy experienceNo. of Openings: 05Skills • Strong knowledge of pharmacology and drug dispensing practices• Accuracy and attention to detail in prescription handling• Good communication and patient counseling skills• Inventory and stock management ability• Understanding of hospital pharmacy operations• Basic computer proficiency for billing and record maintenanceAbout the OrganizationMoolchand Healthcare is one of India’s trusted multi-specialty healthcare institutions, known for delivering high-quality patient care with advanced medical infrastructure and experienced clinical teams.

Roles & Responsibilities• Dispense medications prescribed by physicians accurately and safely• Verify prescriptions for dosage, interactions with other drugs, and patient health conditions• Educate patients on proper usage, potential side effects, and medication risks• Administer vaccinations, including flu shots, where applicable• Advise patients on general health topics such as diet, exercise, and stress management• Complete insurance forms and coordinate with insurance companies for patient medication coverage• Supervise pharmacy technicians, interns, and dispensers in training• Maintain accurate records and perform administrative tasks• Collaborate with other healthcare practitioners on proper medication therapies• Manage multiple patients efficiently while ensuring safety and accuracyQualification• (Bachelor's degree in Pharmacy) B.Pharm, (Master's degree in Pharmacy) M.Pharm, or equivalent pharmacy degreeExperience• Fresher or 1–3 years in pharmacy/dispensing rolesSkills• Accuracy and attention to detail• Strong patient communication skills• Ability to manage multiple patients simultaneously• Knowledge of medication therapies and pharmaceutical regulations• Administrative and record-keeping skillsAbout the CompanyCryptoMize is a Conglomerate Digital Agency operating across 3 continents, serving governments, MNCs, celebrities, and high-net-worth clients in over 30 countries. The company fosters innovation and trains a team of industry experts to deliver high-quality digital and privacy solutions.

Roles & ResponsibilitiesClinical Trial Start-Up• Assist in preparation of study protocols, Investigator’s Brochure, CRFs, and patient information documents• Coordinate with Ethics Committees and Regulatory Authorities for approvals• Conduct site feasibility assessments and support investigator selection• Assist in site initiation and training activitiesTrial Monitoring & Execution• Perform routine on-site monitoring visits• Conduct Source Data Verification (SDV)• Ensure CRF accuracy and regulatory compliance as per ICH-GCP guidelines• Train site staff on study-specific procedures• Manage Investigational Medicinal Product (IMP) accountability• Ensure protocol adherence and subject safetyDocumentation & Close-Out• Prepare monitoring visit reports and follow-up letters• Maintain Trial Master File (TMF) and essential documents• Support audit and inspection readiness• Close trial sites and archive documentation upon study completion• Prepare final reports for sponsors and regulatory authoritiesQualification• Degree in Life Sciences / Medical Sciences / Nursing from a recognized institution• Bachelor of Pharmacy• Master of Pharmacy• Doctor of PharmacyExperience• Minimum 2 years of clinical trial coordination or monitoring experience• Experience in NCD, cardiovascular, or renal trials preferred• Experience in regulatory submissions and ethics committee processesSkills• Strong knowledge of ICH-GCP guidelines• Understanding of regulatory approvals and ethics submissions• Clinical documentation and CRF handling expertise• Site monitoring and stakeholder coordination skills• Willingness to travel for monitoring visits• Excellent English communication and report-writing skillsAbout the OrganizationThe George Institute for Global Health is a globally recognized medical research organization operating in over 40 countries, focused on improving health outcomes worldwide through high-impact research in non-communicable diseases, including cardiovascular, renal, and chronic conditions.

Roles & Responsibilities• Provide technical and strategic support for implementation of national health programs• Offer expert guidance on policy formulation, program design, and health system strengthening• Conduct assessments, data analysis, and prepare technical reports and recommendations• Coordinate with central and state health departments for program execution and monitoring• Support capacity-building initiatives, training, and review meetings• Ensure timely documentation, reporting, and compliance with government guidelines• Assist in research activities, evidence synthesis, and policy briefs• Perform any other duties assigned by the competent authorityQualification• MBBS / BDS / BAMS / BHMS / BUMS / B.Pharm / B.Sc Nursing• Post Graduation in relevant discipline (MPH / MHA / MBA Health / M.Sc or equivalent) preferredExperience• Relevant post-qualification experience in public health programs, health systems, research, or policy implementation preferredSkills• Strong understanding of public health systems and national health programs• Analytical and report-writing skills• Project management and coordination abilities• Good communication and stakeholder engagement skills• Proficiency in computer applications and data analysis toolsAge Limit• Minimum: 21 Years• Maximum: 50 YearsAbout the OrganizationNational Health Systems Resource Centre (NHSRC) is a technical support organization under the Ministry of Health & Family Welfare, Government of India, providing policy, strategy, and implementation support to strengthen public health systems across the country.Last Date of Application: 10-03-2026Official Notification Click Here

Roles & Responsibilities• Lead strategic planning and operational management of assigned divisions• Oversee procurement, supply chain, and quality management activities• Ensure regulatory compliance and adherence to organizational policies• Monitor performance metrics and drive process improvements• Coordinate with government agencies, vendors, and internal stakeholders• Supervise budgeting, financial planning, and resource allocation• Provide leadership to cross-functional teams and ensure timely project execution• Prepare reports, policy notes, and management updates for senior authoritiesQualification• M.Pharm (Master of Pharmacy) or M.Sc from a recognized universityExperience• Relevant senior-level managerial/administrative experience in pharmaceuticals, procurement, supply chain, or public health systems (as per organizational norms)Skills• Strong leadership and strategic management capabilities• Knowledge of pharmaceutical procurement and supply chain systems• Understanding of regulatory and quality compliance frameworks• Excellent coordination and stakeholder management skills• Strong analytical, reporting, and decision-making abilities• Proficiency in computer applications and office toolsNo. of Vacancy: 01Age Limit• Minimum: 21 Years• Maximum: 56 YearsImportant Date• Last Date of Application: 10-03-2026About the OrganizationThe Central Medical Services Society (CMSS) functions under the Ministry of Health & Family Welfare, Government of India, and is responsible for centralized procurement and distribution of essential medicines and medical supplies for national health programs.Official Notification and Application Form Click Here

Roles & Responsibilities• Lead and manage pharmacovigilance activities across assigned projects• Oversee signal detection, aggregate reporting, risk management, and safety compliance functions• Provide technical guidance and act as Subject Matter Expert (SME) for PV operations• Ensure adherence to global pharmacovigilance regulations and SOPs• Review safety data, perform quality oversight, and ensure regulatory timelines are met• Mentor and support team members in PV processes and best practices• Coordinate with cross-functional stakeholders and clients for safety deliverables• Drive process improvements and ensure high-quality safety outputsQualification• M.Pharm / Pharm.D / BDSExperience• 3–5 years of comprehensive Pharmacovigilance experience• Experience across multiple PV functions beyond only ICSR processing• Leadership or SME exposure preferred• Candidates returning after a career break with relevant PV expertise may applySkills• Strong knowledge of global PV regulations (ICH, GVP)• Expertise in aggregate reporting, signal management, and risk evaluation• Team leadership and mentoring skills• Strong analytical and problem-solving abilities• Excellent communication and stakeholder management skills• Quality and compliance-focused mindsetAbout the CompanyAccenture is a clinical research and pharmacovigilance services organization focused on delivering high-quality safety and regulatory solutions to pharmaceutical clients. The company promotes a collaborative, growth-oriented work culture and offers leadership opportunities for experienced pharmacovigilance professionals in a full-time, office-based role in Delhi/NCR.

Roles & Responsibilities• Provide technical and strategic guidance for national health programs and policy implementation• Support planning, monitoring, and evaluation of public health initiatives• Coordinate with government bodies, stakeholders, and healthcare institutions• Develop reports, policy briefs, and technical documentation• Conduct data analysis and provide evidence-based recommendations• Ensure compliance with national health standards and program guidelinesQualification• MBBS / BDS / BAMS / BHMS / BUMS / B.Pharm /Nursing• Post Graduation in relevant fieldExperience• As per NHSRC norms for Senior Consultant position• Relevant experience in public health, healthcare management, or national health programs preferredVacancies• 01 Senior ConsultantSkills• Strong knowledge of public health systems and national health programs• Policy analysis and strategic planning skills• Data interpretation and report writing expertise• Stakeholder coordination and communication skills• Leadership and project management abilitiesAbout the CompanyNational Health Systems Resource Centre (NHSRC) is a premier technical support organization under the Ministry of Health & Family Welfare, Government of India. It provides policy and implementation support to strengthen public health systems across the country. NHSRC plays a key role in advising on national health missions, healthcare reforms, and capacity building initiatives to improve healthcare delivery nationwide.Last Date of Application - 10-03-2026Official Notification - Click Here

Roles & Responsibilities• Assist in preparation of protocol, Investigator’s Brochure, CRF, and patient information documents• Coordinate with Ethics Committees and Regulatory Authorities for submissions and approvals• Conduct site feasibility assessments and support investigator selection and site initiation• Perform on-site monitoring visits and Source Data Verification (SDV)• Ensure CRF accuracy, regulatory compliance, and adherence to ICH-GCP guidelines• Train site staff on study-specific procedures and protocol requirements• Manage Investigational Medicinal Product (IMP) accountability• Prepare monitoring visit reports and maintain trial documentation• Archive study documents and prepare final reports for sponsors and authorities• Support site close-out activities upon study completionQualification• B.Pharm / M.Pharm / Pharm.D / Life Sciences / Medical Sciences / NursingExperience• Minimum 2 years of clinical trial coordination or clinical research experience• Experience in site monitoring, ethics submissions, and regulatory coordination• Knowledge of ICH-GCP and clinical documentation practicesSkills• Strong understanding of ICH-GCP guidelines and regulatory processes• Experience in CRF handling and clinical documentation management• Ability to coordinate with multi-site stakeholders• Willingness to travel for site monitoring visits• Excellent English communication skills• Strong organizational and time management abilitiesAbout the CompanyThe George Institute for Global Health is a globally recognized medical research organization affiliated with leading universities and operating in more than 40 countries. With a strong focus on non-communicable diseases such as cardiovascular, renal, and chronic disorders, the institute conducts large-scale international clinical trials aimed at improving global health outcomes. It promotes diversity, ethical research standards, and collaborative clinical research excellence.

Roles & Responsibilities:• Conduct and oversee site initiation, interim monitoring, and close-out visits according to study protocols, GCP, and applicable regulatory guidelines• Build and maintain strong professional relationships with investigators, site coordinators, and key stakeholders• Proactively identify and resolve site issues to ensure quality and compliance• Perform comprehensive monitoring visits to assess site performance, data accuracy, and adherence to protocol• Ensure timely follow-up on monitoring findings, query resolution, and documentation in compliance with SOPs• Support risk-based monitoring activities and provide oversight to ensure data reliability• Ensure all trial activities comply with study protocols, SOPs, and local/international regulations• Participate in preparation and review of regulatory submissions and ethics committee communications• Monitor, document, and report adverse events according to safety protocols and regulatory timelines• Collaborate with data management and project teams to maintain high data quality and consistency• Participate in internal and external audits, ensuring readiness and corrective actions as needed• Provide ongoing training, mentoring, and support to site staff and junior CRAs• Serve as a subject matter expert for protocol-related and operational queriesQualification:• Bachelor of Pharmacy, Master of Pharmacy• Bachelor’s or Master’s degree in Life Sciences or a related fieldExperience:• Minimum 3 years as a Clinical Research Associate with demonstrated success in independently managing clinical sitesSkills:• Strong understanding of ICH-GCP, local and international regulatory requirements, and clinical trial conduct• Excellent communication and interpersonal abilities• Strong analytical, organizational, and problem-solving skills• Proficiency in documentation, reporting, and time management• Ability to work independently and collaboratively within cross-functional teams• Willingness to travel extensively to investigative sitesAbout the Organization:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific innovation and improving healthcare outcomes through high-quality clinical trials that meet global standards.

Roles & Responsibilities• Coordinate day-to-day clinical trial activities at the study site• Assist investigators in patient screening, recruitment, and follow-up visits• Maintain and update Trial Master File (TMF) and essential study documents• Ensure compliance with ICH-GCP guidelines and approved study protocols• Support and document the informed consent process• Perform data entry and resolve queries in CRF/eCRF systems• Communicate with sponsors, CROs, and ethics committees• Prepare study reports and maintain regulatory documentation• Support monitoring visits and auditsQualification• B.Sc / M.Sc or equivalent degree in Life Sciences• Master of PharmacyExperience• Minimum 1 year of clinical research experience• Experience in site coordination and clinical trial documentation preferredSkills• Understanding of clinical trial processes• Basic knowledge of ICH-GCP guidelines• Strong documentation skills• Proficiency in CRF/eCRF systems• Good communication and coordination abilities• Attention to detail and compliance awarenessAbout the OrganizationA leading clinical research services provider based in Delhi, India, offering structured clinical trial management solutions. The organization provides strong exposure to clinical operations, regulatory documentation, and sponsor coordination within a professional research environment.

Roles & Responsibilities• Assist Principal Investigator (PI) in site feasibility and study start-up activities• Prepare and maintain regulatory documents (CVs, Financial Disclosure, PI Undertaking, Confidentiality Agreements)• Coordinate IRB/IEC submissions, safety reports, amendments, and progress reports• Support informed consent process and prepare for Site Initiation Visits (SIV)• Maintain Site Master File (SMF), patient files, screening & enrollment logs• Manage patient pre-screening, recruitment, follow-ups, and visit coordination• Ensure accurate CRF completion and clinical data entry• Perform SAE reporting and follow-up activities• Maintain drug accountability and inventory records• Track study budgets, IRB fees, invoices, lab costs, and patient reimbursementsQualification• Any Graduate (Life Sciences / Pharmacy preferred)Experience• 1–4 years of experience in clinical research or clinical trial coordinationSkills• Strong knowledge of ICH-GCP guidelines• Experience in IRB/IEC submissions and regulatory documentation• SAE reporting and drug safety awareness• CRF completion and clinical data management• Patient recruitment and site coordination skills• Good communication, documentation, and organizational abilityAbout the OrganizationMax Healthcare is one of India’s leading hospital networks, known for excellence in patient care and advanced medical research. The organization offers strong exposure to investigator-initiated and sponsored clinical studies within a reputed hospital research environment.