Pharmacy Jobs

Role & Responsibilities • Process and triage Individual Case Safety Reports (ICSRs) • Ensure data accuracy, completeness, and regulatory compliance in safety reporting • Perform medical coding of adverse events, medical history, and medications using MedDRA • Support xEVMPD submissions and SPOR/IDMP activities • Maintain documentation within TMF and Pharmacovigilance system master files • Collaborate with global safety teams to meet regulatory timelines Qualification • Degree in Pharmacy, Life Sciences, or related healthcare discipline (e.g., B.Pharm, M.Pharm, Pharm.D, MSc, BDS) Experience • 2.6 to 4.5 years of hands-on experience in ICSR case processing • Proven experience with Argus, ArisG, or LSMV safety databases • Strong understanding of global pharmacovigilance regulations • Knowledge of MedDRA coding and safety reporting workflows Skills • Expertise in pharmacovigilance and safety reporting • Ability to manage and maintain accurate documentation • Strong collaboration and communication skills in a global setting About The Company • Syneos Health – A global biopharmaceutical solutions organization, Syneos Health provides a full spectrum of clinical, medical affairs, and commercialization services. The company is committed to delivering innovative solutions across the drug development lifecycle, from preclinical to post-marketing. Syneos Health fosters a collaborative work culture with global exposure and career growth opportunities.

Role & Responsibilities • Lead medical affairs objectives in the assigned country, serving as an internal medical, technical, and scientific resource • Use medical and scientific information to facilitate physician engagement on clinical and scientific issues relevant to AbbVie’s products • Identify and develop professional relationships with thought leaders, academic centers, and researchers in assigned therapeutic areas • Work closely with commercial leaders and medical affairs teams to set priorities and define strategies • Present AbbVie product data to healthcare professionals, academic institutions, and researchers upon request • Support research initiatives, collaborating with AbbVie R&D, Clinical Operations, and Medical Affairs departments • Develop scientifically accurate, balanced, and compliant disease-state and product communications • Support Round Table and Advisory Board sessions to ensure the accuracy of clinical data • Conduct ongoing training for internal teams, including medical affairs and field sales • Travel approximately 60% of the time for field-based activities, serving as the local representative of the Global Medical Office Qualification • MD, MBBS, or Pharm D Experience • 2-3 years of post-qualification experience in the Medical Affairs function • Experience within the pharmaceutical industry or clinical research is preferred • Ability to work cross-functionally in a matrix structure and support multiple stakeholders • Strong presentation and teaching skills to convey technical information effectively • Demonstrated ability to develop and maintain strong relationships with key stakeholders • Experience in evaluating and communicating clinical data effectively Skills • Ability to convey complex scientific and clinical data to individuals with varying scientific knowledge • Strong analytical and problem-solving skills • Proficiency with technology and systems like Microsoft Office About The Company • AbbVie – A global leader in the pharmaceutical industry, AbbVie is committed to delivering innovative medicines that solve serious health issues today and address tomorrow’s challenges. The company is deeply involved in multiple therapeutic areas including immunology, oncology, neuroscience, and eye care, with a commitment to improving lives through advanced treatments and solutions.

Role & Responsibilities • Independently manage multiple sites and complex clinical studies • Lead site monitoring activities and ensure protocol and regulatory compliance • Drive data quality, patient safety, and risk mitigation strategies • Mentor and guide junior CRAs • Support audits, inspections, and cross-functional collaboration Qualification • Life Sciences graduate/postgraduate Experience • 5-6 years of experience as a Clinical Research Associate (CRA) • Extensive CRA experience, with a strong expertise in GCP, regulatory guidelines, and monitoring best practices • Proven ability to manage sites independently and handle escalations Skills • Strong communication, coordination, and documentation skills • Excellent leadership, stakeholder management, and problem-solving skills About The Company • Sanofi Careers - Leading global healthcare company providing medicines and treatments across diverse therapeutic areas

Role & Responsibilities • Independently manage multiple sites and complex clinical studies • Lead site monitoring activities ensuring protocol, GCP, and regulatory compliance • Review monitoring reports, SDV quality, and site performance metrics • Support junior CRAs through mentoring and guidance • Proactively identify risks and drive issue resolution and escalation • Ensure inspection readiness and high-quality TMF maintenance Qualification • Graduate or Postgraduate in Life Sciences • Pharmacy, Biotechnology, Nursing, or related disciplines Experience • 5–6 years of clinical research monitoring experience Skills • Strong expertise in ICH-GCP and global clinical trial regulations • Leadership and stakeholder management skills • Ability to manage complex studies independently • Excellent analytical, communication, and documentation skills About the Company • Sanofi is a leading global healthcare company committed to advancing clinical research to deliver innovative therapies and improve patient outcomes worldwide

Role & Responsibilities • Execute site monitoring activities in line with study protocol, SOPs, ICH-GCP, and regulatory requirements • Conduct site initiation, routine monitoring, and close-out visits • Perform source data verification (SDV) and ensure data accuracy and quality • Ensure timely query resolution and compliance with study timelines • Maintain essential documents and Trial Master File (TMF) • Build and maintain strong relationships with investigators and site teams Qualification • Graduate or Postgraduate in Life Sciences • Pharmacy, Biotechnology, Nursing, or related disciplines Experience • 1–3 years of experience as a Clinical Research Associate or similar role Skills • Strong knowledge of ICH-GCP and clinical trial processes • Excellent communication and coordination skills • Good documentation and reporting abilities • Willingness to travel as per study requirements About the Company • Sanofi is a global biopharmaceutical company focused on transforming patient lives through innovative clinical research and development

Roles & Responsibilities:• Convert healthcare text information into numeric Diagnosis (Medical Problems) and Procedure (Treatments) Codes using ICD-10 CM and CPT code books• Analyze patient records, clinical reports, and other healthcare documentation for accurate coding• Maintain accuracy and compliance with coding standards and regulations• Communicate with healthcare professionals for clarification of documentation when needed• Maintain proper records of coded data and submit reports as per company guidelines• Assist in audits and quality checks to ensure coding accuracy• Participate in training and professional development programs for medical coding updates• Adhere to organizational protocols, confidentiality, and compliance policiesQualification:• UG: Nursing (GNM/DGNM), Life Sciences, Pharmacy, Physiotherapy, Dentistry (BDS), BHMS, BUMS, B.Sc in Food Technology, Optometry, Home Science, Bio-Chemistry, Biology, Microbiology, Botany, Nursing, Chemistry, Zoology, Environmental Science, BVSC, B.Tech/B.E. in Bio-Chemistry/Bio-Technology, Biomedical, B.Pharma, BAMS• PG: MVSC, MDS, MS/M.Sc(Science) in Food Technology, Biotechnology, Organic Chemistry, Home Science, Optometry, Microbiology, Nursing, Zoology, Bio-Chemistry, Biology, Botany, Chemistry, Environmental Science, Veterinary Science, M.Pharma, M.Tech in Environmental, Bio-Chemistry/Bio-Technology, BiomedicalExperience:• 0 – 2 years (Freshers with relevant knowledge can apply)Skills:• Knowledge of Anatomy and Physiology• Medical coding using ICD-10 CM and CPT codes• Basic computer skills and documentation• Communication and interpersonal skills• Attention to detail and accuracy• Ability to work in a fast-paced environment• Female/male nurse, GNM/DGNM, dietetics, biotechnology, pharmacy, biology, nutrition, physiotherapy, pharmacist, microbiology, botany, biomedical, bioinformatics, staff nurse, midwiferyPerks and Benefits:• Performance-based incentives and benefits as per corporate standards• Pick-up & drop facility• Food facility• Day shift• Weekend off• 4K fixed hike after six monthsAbout the Company:• Achievers Spot is an organization offering medical coding and billing services with a focus on revenue cycle management. The company provides career opportunities for freshers in nursing, life sciences, pharmacy, physiotherapy, biomedical, biotechnology, and related fields. Achievers Spot emphasizes accuracy, professional development, and excellence in healthcare documentation and coding services.

Roles & Responsibilities:• Convert healthcare text information into numeric Diagnosis and Procedure Codes using ICD-10 CM and CPT codes• Ensure accuracy in medical coding for patient records, billing, and reporting• Support healthcare billing and revenue cycle management processes• Collaborate with medical staff to clarify and verify clinical documentation• Maintain compliance with coding standards and regulations• Assist in auditing and quality checks of coded dataQualifications:• UG: BVSC, BAMS, BUMS, B.Tech/B.E. in Biochemistry/Biotechnology/Biomedical, B.Sc in Food Technology, Optometry, Biochemistry, Biology, Microbiology, Botany, Nursing, Chemistry, BHMS, MBBS, BDS, B.Pharma,BPT.• PG: M.Tech in Biochemistry/Biotechnology/Biomedical, MDS, MS/M.Sc (Science) in Food Technology, Biotechnology, Organic Chemistry, Optometry, Biochemistry, Biology, Microbiology, Botany, Nursing, Zoology, Veterinary Science, MVSC, M.PharmaExperience:• Freshers with relevant UG/PG qualification in life sciences, paramedical, or medical streamsSkills:• Knowledge of pharmacy, paramedical, microbiology, physiotherapy, biomedical engineering, nutrition, dietetics, and medical sciences• Familiarity with medical coding standards, ICD-10 CM, and CPT codes• Analytical, detail-oriented, and accurate in documentation• Good communication and collaboration skills• Ability to work under deadlines and in a healthcare environmentAbout the Company:Achievers Spot is an organization specializing in Medical Coding and Billing services, helping healthcare providers achieve outstanding results in revenue cycle management. The company focuses on accurate, efficient, and compliant coding and billing processes while providing professional growth opportunities to employees.

Role & Responsibilities • Perform medical review of aggregate safety reports to ensure accuracy, consistency, and regulatory compliance • Review and assess Individual Case Safety Reports (ICSRs) in line with global pharmacovigilance standards • Analyse signal reports and provide medical interpretation, insights, and recommendations • Contribute to the preparation, review, and maintenance of Risk Management Plans (RMPs) • Support benefit–risk evaluation activities for assigned products • Ensure compliance with global PV regulations, guidelines, and internal SOPs • Collaborate with cross-functional teams including PV operations, regulatory affairs, and quality • Maintain high standards of documentation, medical judgment, and review quality Qualification • MBBS or MD Experience • Minimum 2+ years of experience in Drug Safety / Pharmacovigilance / Medical Review Skills • Strong understanding of pharmacovigilance processes and safety reporting • Knowledge of aggregate reports, signal detection, and risk management activities • Familiarity with global PV regulations and guidelines • Strong analytical, medical review, and documentation skills • Ability to work effectively in an office-based, cross-functional environment About the Company • Fresenius Kabi Oncology Limited is part of a global healthcare group dedicated to advancing life-saving medicines and technologies

Roles & Responsibilities • Carry out effective field work to achieve and exceed assigned sales budgets through prescription generation from HCPs • Conduct effective RCPA, ensure accurate data entry, and prepare pre-call objectives for every doctor visit • Demonstrate and promote products to doctors and pharmacists as per division guidelines • Build strong relationships with customers to ensure regular conversion and prevent prescriber loss • Ensure adequate product availability at pharmacies and generate required POBs as per division norms • Create and regularly update doctor and chemist lists as per division guidelines • Support and ensure successful execution of new product launches • Manage and coordinate with distribution channel members such as stockists Qualifications • B.Sc / B.Pharm / D.Pharm / MBA Experience • 0 to 4 years of experience in pharmaceutical sales or field force roles Skills • Basic scientific and product knowledge • Good communication and interpersonal skills • Strong planning and execution capability • Willingness to travel and relocate anywhere in India • Two-wheeler with valid driving license is mandatory About the Organisation Alembic Pharmaceuticals is a leading Indian pharmaceutical company with a strong domestic and international presence, known for quality-driven manufacturing, ethical marketing practices, and continuous innovation in healthcare solutions.

Roles & Responsibilities • Implement marketing strategies and promotional campaigns for medical device, pharma, and OTC products • Drive product promotion through effective in-clinic presentations to doctors • Identify and promote the right products for the right doctors and institutions • Monitor retail chemist prescription audits and secondary sales • Lead, guide, and motivate a team of ABMs and MRs to achieve business objectives • Ensure timely reporting, territory reviews, and performance tracking • Achieve assigned value and volume targets for the region Qualifications • B.Sc or B.Pharm Experience • Minimum 1 year experience as a 2nd line manager • Proven experience handling a team of ABMs and MRs • Exposure to OTC and Pharma segments is mandatory • Experience in medical devices will be an added advantage Skills • Strong people management and leadership skills • Effective communication, presentation, and negotiation abilities • Strategic thinking with strong execution capability • Target-driven with proven regional performance About the Organisation APLE Pharma is a growing pharmaceutical organization with a presence across pharma, OTC, and medical device segments, focused on ethical promotion, innovation, and building strong relationships with healthcare professionals.

Roles & Responsibilities • Implement marketing strategies and promotional campaigns for assigned products • Promote products to doctors through effective in-clinic presentations • Identify and promote the right products to the right doctors • Conduct retail chemist prescription audits and collect market feedback • Ensure timely reporting of daily field activities • Achieve assigned value and volume sales targets Qualifications • B.Sc or B.Pharm Experience • Minimum 1 year experience in pharmaceutical ethical selling • Experience in Derma and/or Disinfectant segment preferred Skills • High energy level and strong field orientation • Effective communication, presentation, and convincing skills • Strong relationship-building ability • Proven track record of achieving sales targets About the Organisation A growing pharmaceutical organization with a strong focus on ethical promotion and a developing presence in the Derma and Disinfectant segments, committed to quality products and long-term partnerships with healthcare professionals.

Roles & Responsibilities: • Implement marketing strategies and promotional campaigns for assigned products • Conduct effective in-clinic product presentations to doctors • Identify and promote the right products to the right doctors • Generate prescriptions through ethical promotion practices • Conduct retail chemist prescription audits • Ensure timely reporting of field activities • Achieve assigned value and volume sales targets Qualifications: • B.Sc or B.Pharma Experience: • Minimum 1 year experience in pharma ethical selling preferred Skills: • Strong communication, presentation, and convincing skills • High energy level with result-oriented approach • Ability to build strong relationships with doctors and chemists • Proven track record of achieving sales targets About the Organization: APLE PHARMA is a growing pharmaceutical company engaged in marketing quality healthcare products across multiple therapeutic segments, with a strong focus on ethical promotion and field excellence.

Role & Responsibilities • Contribute to a culture of process improvement and operational excellence • Review and process Serious Adverse Events (SAEs), spontaneous ADRs, and safety data • Perform safety review of clinical and diagnostic data • Ensure case processing accuracy as per SOPs, study procedures, regulatory and sponsor requirements • Maintain and review safety tracking systems for data quality and compliance • Liaise with investigational sites, reporters, sponsors, and cross-functional teams on safety issues • Attend project team meetings and sponsor teleconferences as required • Serve as a safety resource for investigational sites and internal teams • Assist in training and mentoring junior Drug Safety Associates • Support generation of study-specific procedures and identify out-of-scope activities • Act as Lead Drug Safety Associate for local or regional projects • Support MSS Functional Lead under supervision • Travel up to 10% (domestic/international) as required Qualification • Life Sciences / Pharmacy / Healthcare background preferred Experience • 4–10 years of experience in Pharmacovigilance / Drug Safety • Experience in Pharma, Biotech, CRO, or Clinical Research environments Skills • Strong knowledge of Pharmacovigilance processes • Hands-on experience with Oracle Argus • Knowledge of EudraVigilance and global safety databases • Exposure to aggregate reporting activities • Strong attention to detail and data quality focus • Effective communication and stakeholder coordination skills • Ability to work independently and lead safety activities About the Company • Covalent Trainings specialises in pharmacovigilance training and industry placements, Supports global PV projects across pharma, biotech, and CRO sectors

Roles & Responsibilities: • Meet doctors and chemists to promote pharmaceutical products • Handle general and multi-specialty segment product promotion • Build and maintain strong relationships with doctors, chemists, and distributors • Achieve sales targets and ensure effective product positioning • Collect market feedback and share insights with management • Ensure regular follow-ups and complete territory coverage Qualifications: • B.Sc, B.Pharma, or any graduate preferred Experience: • 0–3 years experience in meeting doctors and chemists • Freshers with strong communication skills can also apply Skills: • Strong communication and presentation skills • Sales and negotiation abilities • Relationship-building with healthcare professionals • Willingness to travel within assigned territory • Self-motivated and result-oriented About the Organization: L K Saddi Associates is a pharmaceutical marketing and recruitment organization focused on promoting quality pharma products through strong doctor and chemist engagement across multiple segments.

Roles & Responsibilities: • Develop and implement innovative solutions using analytical and problem-solving skills • Collaborate with cross-functional teams to achieve business objectives • Conduct market research and analyze data to identify trends and opportunities • Provide customer service and support to clients and stakeholders • Stay updated with industry developments and emerging technologies • Participate in training and skill development programs Qualifications: • D Pharma, B Pharma, B.Sc, M.Sc, or B.Tech Experience: • 0–4 years in Pharma, Biotech, or Life Sciences industry preferred Skills: • Strong knowledge of pharmaceutical and life sciences concepts • Excellent communication and interpersonal skills • Strong analytical and problem-solving abilities • Ability to work in a fast-paced environment and meet deadlines • Familiarity with medical terminology and healthcare practices • Knowledge of chemical compounds and food products • Innovative mindset and critical thinking ability About the Organization: Leading Client is a reputed organization operating in the pharmaceutical and life sciences sector, focused on innovation, quality, and delivering value-driven healthcare solutions in a dynamic and collaborative work environment.

Roles & Responsibilities: • Ensure MAH pharmacovigilance compliance with EU GVP Modules and UK MHRA requirements • Act as operational PV representative for UK and EU markets • Support QPPV / UK QPPV in maintaining PV system oversight • Ensure PV agreements with partners, distributors, and service providers are in place • Provide oversight of outsourced PV providers (ICSRs, literature, signals, aggregate reports) • Monitor vendor performance against KPIs and SLAs and lead governance meetings • Ensure timely and compliant ICSR reporting to EudraVigilance, MHRA, and partners • Oversee PSUR/PBRERs, RMPs, signal management, and benefit–risk evaluations • Maintain MAH PV Quality Management System and ensure SOP compliance • Support PV inspections and audits (MHRA, EMA, partners) and manage CAPAs • Act as PV contact for Regulatory, Quality, and Commercial teams • Ensure safety information is accurately reflected in SmPC, PIL, and submissions Qualifications: • M.Pharma in Pharmacy Experience: • Proven pharmacovigilance experience within UK and/or EU • Experience working in an MAH environment • Hands-on experience managing outsourced/third-party PV providers Skills: • Strong regulatory and compliance mindset • Excellent vendor and stakeholder management skills • Strong documentation, review, and inspection readiness abilities • Ability to work independently and manage multiple priorities • Experience in generics and post-marketing PV • Exposure to global PV operations and EudraVigilance systems About the Organization: B&S Group is a global distribution and supply chain organization operating across pharmaceuticals and healthcare, with a strong focus on regulatory compliance, quality, and patient safety across international markets.

Roles & Responsibilities: • Report safety information from India and India cluster (South Asia countries) to Global Safety • Follow up with reporters for additional safety information • Review and manage safety mailbox for incoming reports • Perform monthly reconciliation and compliance checks from a pharmacovigilance perspective • Prepare and submit Periodic Safety Update Reports (PSURs) to regulatory authorities as per regulations • Gather requirements and prepare regulatory dossiers for new products, clinical trials, variations, and renewals • Prepare responses to regulatory authority queries and coordinate with global teams • Support preparation for regulatory authority and expert committee meetings • Prepare and follow up on regulatory submissions for South Asia countries • Prepare and update product labeling materials • Review promotional materials for compliance with approved product registrations • Ensure timely updates to regulatory databases • Update and maintain local SOPs • Update and renew safety agreements with partners, manufacturers, and distributors • Coordinate price updates and ensure timely entry into NPPA pricing database • Manage lifecycle maintenance activities and update commercial teams on key milestones Qualifications: • Bachelor’s degree in Pharmacy, Life Sciences, Microbiology, Chemistry, or related field Experience: • Minimum 1+ year experience in India Regulatory Affairs and Pharmacovigilance • Experience within pharmaceutical or biotechnology industry preferred Skills: • Knowledge of Indian regulatory and pharmacovigilance requirements • Strong documentation and dossier preparation skills • Ability to coordinate with global and cross-functional teams • Good communication and regulatory compliance understanding • Attention to detail and ability to manage multiple submissions About the Organization: Ferring Therapeutics is a global, research-driven biopharmaceutical company committed to developing innovative treatments in areas of high unmet medical need. The company focuses on maintaining the highest standards of quality, regulatory compliance, and patient safety while delivering life-changing therapies worldwide.

Roles & Responsibilities: • Perform medical assessments of client’s product ranges and evaluate adverse events • Conduct medical reviews of aggregate reports and prepare clinical expert statements • Detect signals for client’s medicinal products and manage risk management plans • Provide guidance and participate in follow-up of adverse events, offering backup medical support • Interact with staff at various levels to resolve issues during reviews • Contribute to enhancing pharmacovigilance processes and writing SOPs • Ensure compliance with local regulations and global pharmacovigilance requirements • Assist in developing SOPs for the department and clients, and communicate with clients and regulatory agencies if needed Qualifications: • Relevant degree in Life Sciences, Pharmacy, or related field Experience: • 0–1 year in pharmacovigilance or related field Skills: • Knowledge of local and national pharmacovigilance requirements • Strong communication and client interaction skills • Ability to work effectively with staff at various levels and functional areas • Marketing, business generation, direct sales, and client servicing skills About the Organization: This organization is a dynamic employment and recruitment services firm providing specialized healthcare and pharmacovigilance staffing solutions. They focus on regulatory compliance, quality processes, and client satisfaction while fostering a collaborative environment for professional growth.

Roles & Responsibilities: • Prepare and review clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and other clinical trial documents in line with regulatory guidelines and industry standards • Collaborate with cross-functional teams, including clinical operations, regulatory affairs, and biostatistics, to ensure accuracy and completeness of deliverables • Interpret and summarize clinical trial data from study reports, statistical analyses, and scientific literature • Assist in preparation of regulatory submissions (INDs, NDAs, BLAs, MAAs) with high-quality medical writing support • Participate in project meetings, provide updates on medical writing activities, and contribute to project planning and timelines • Stay current with developments in medical writing, regulatory requirements, and therapeutic areas relevant to projects • Mentor junior medical writers and provide guidance on best practices for document preparation Qualifications: • Bachelor’s degree in Life Sciences, Pharmacy, or related field; advanced degree (MD, PhD, PharmD) preferred Experience: • Minimum 5 years of experience in medical writing within pharmaceutical, biotechnology, or CRO industry • Proficiency in interpreting clinical trial data, including statistical analyses and safety reports • Strong understanding of regulatory guidelines (ICH, FDA, EMA) for clinical trial documents and submissions Skills: • Excellent written and verbal communication skills • Detail-oriented with strong organizational and time management abilities • Ability to work independently and collaboratively in multidisciplinary teams • Proficiency in Microsoft Office Suite and familiarity with document management systems (e.g., SharePoint) About the Organization: MS Clinical Research Pvt Ltd is a dynamic and innovative clinical research organization specializing in clinical trials and comprehensive medical writing services. The company is committed to advancing medical research, supporting regulatory submissions, and improving patient outcomes through high-quality, scientifically accurate documentation and collaborative project execution.