Doctor Jobs in Pune

Why This Role MattersIn modern healthcare systems, patients often require prior approval from insurance providers before certain medications or treatments can be dispensed. This process, known as prescription prior authorization, ensures that therapies are medically necessary, safe, and aligned with insurance coverage policies. Without proper authorization, patients may face delays in receiving essential medications or incur higher treatment costs.The role of a Prescription Prior Authorization Specialist is crucial in bridging the gap between healthcare providers, insurance companies, pharmacies, and patients. By coordinating authorization requests and verifying coverage requirements, professionals in this role help ensure that patients receive timely access to prescribed medications.Pharmacy professionals bring valuable knowledge to this position because they understand drug therapy, prescription processes, and healthcare documentation. Their expertise allows them to interpret prescription requirements, communicate effectively with healthcare teams, and navigate authorization systems efficiently. This role supports patient care while improving administrative efficiency within healthcare organizations.Job DescriptionThe Prescription Prior Authorization Specialist is responsible for managing medication authorization requests, verifying insurance requirements, and coordinating with healthcare providers and insurers to obtain approval for treatments. The position involves reviewing prescription information, preparing required documentation, and submitting authorization requests to insurance companies or pharmacy benefit managers.Professionals in this role track authorization statuses, resolve issues related to coverage approvals, and ensure that all documentation complies with healthcare regulations. The specialist also communicates regularly with physicians, clinical staff, and patients to provide updates on authorization progress and requirements.This position is well suited for pharmacy graduates who are interested in healthcare support services, medical billing, pharmacy benefit management, or healthcare administration. It offers a structured career path within healthcare operations and insurance coordination while maintaining a strong connection to pharmacy practice.Key Features of the RoleThe role offers pharmacy professionals an opportunity to work in healthcare support services where they can apply their knowledge of medications, prescriptions, and healthcare documentation. Professionals in this position collaborate with multiple stakeholders, including healthcare providers, insurance companies, and patient support teams, to facilitate medication approvals.The job also involves working with healthcare documentation systems and insurance authorization workflows, helping professionals develop strong administrative, analytical, and communication skills. It provides exposure to pharmacy benefit management and healthcare insurance processes, which are growing sectors within the healthcare industry.Responsibilities• Managing prior authorization requests for medications and treatments.• Coordinating with healthcare providers, insurance companies, and patients.• Verifying insurance coverage and authorization requirements.• Preparing and submitting prior authorization documentation.• Tracking authorization status and ensuring timely approvals.• Communicating updates and requirements with physicians and clinical teams.• Maintaining accurate documentation and compliance with healthcare regulations.• Resolving authorization issues and following up on pending approvals.• Handling multiple authorization cases simultaneously while ensuring accuracy.• Ensuring adherence to organizational procedures and healthcare compliance standards.Required QualificationsEducational Requirements• Bachelor of Pharmacy (B.Pharm)• Diploma in Pharmacy (D.Pharm)Experience and Skills• Minimum 1 year of experience in prescription prior authorization or related healthcare support roles.• Knowledge of prior authorization workflows and insurance approval processes.• Strong written and verbal communication skills.• Ability to coordinate with insurers, physicians, and healthcare teams.• Excellent organizational and multitasking abilities.• Familiarity with healthcare documentation and regulatory compliance standards.• Attention to detail in reviewing prescription and authorization documentation.• Ability to track multiple cases and manage deadlines efficiently.• Strong problem-solving skills for resolving authorization issues.Salary InsightsThe salary offered for the Prescription Prior Authorization Specialist role typically depends on the candidate’s experience, skill level, and the hiring organization’s policies.Estimated salary range:• ₹2,80,000 – ₹4,50,000 per yearAdditional benefits may include:• Exposure to healthcare support and insurance coordination processes.• Professional development opportunities in medical billing and healthcare administration.• Stable career growth in pharmacy benefit management and healthcare operations.• Opportunities to work with healthcare providers, insurers, and clinical teams.Company OverviewHealthcare service organizations that hire Prescription Prior Authorization Specialists typically support hospitals, pharmacies, insurance companies, and healthcare providers in managing medication approval processes. These organizations help streamline administrative workflows and ensure patients receive medications without unnecessary delays. Such companies often specialize in medical billing, pharmacy benefit management, healthcare documentation, and insurance coordination services. By managing authorization processes efficiently, they play a critical role in improving healthcare delivery and ensuring regulatory compliance.FAQs1. What does a Prescription Prior Authorization Specialist do?They manage authorization requests for medications and treatments, coordinate with insurers and healthcare providers, and ensure approvals are processed efficiently.2. Who can apply for this role?Candidates with D.Pharm or B.Pharm qualifications and experience in prior authorization processes are eligible.3. Is prior authorization experience mandatory?Yes, most employers prefer candidates with at least one year of experience in prior authorization or related healthcare support roles.4. What career opportunities are available after this role?Professionals can advance to positions such as Senior Authorization Specialist, Healthcare Operations Analyst, Medical Billing Specialist, or Pharmacy Benefit Management Professional.Application Tips• Highlight your knowledge of prescription workflows and healthcare documentation.• Emphasize experience in prior authorization or insurance coordination.• Showcase strong communication skills for interacting with healthcare providers and insurers.• Demonstrate your ability to manage multiple cases while maintaining accuracy.• Mention any experience with healthcare management systems or insurance platforms.

Why This Role MattersThe Clinical Safety Associate plays a crucial role in protecting patient health by ensuring the accurate collection, processing, and reporting of adverse event data from clinical trials and post-marketing sources. This position directly supports pharmacovigilance and Patient Safety Services (PSS) operations by managing expedited safety reports and maintaining regulatory compliance. Timely and accurate safety reporting is essential to meet global regulatory standards and to ensure that medicinal products remain safe for public use. By contributing to the end-to-end adverse event lifecycle, this role supports quality clinical research and strengthens trust between sponsors, regulatory authorities, and patients.Job DescriptionThe Clinical Safety Associate assists with overall Clinical Safety and PSS operations associated with pharmaceutical products. The role involves managing the entire adverse event process, including safety data collected from clinical trials and unsolicited post-marketing reports. The associate is responsible for processing expedited adverse events according to regulatory standards and submitting them to clients and regulatory authorities within agreed timelines. This position may function as part of a client project support team or operate as a standalone safety service provider. The role requires adherence to health, safety, and quality regulations as outlined in company policies and applicable legal frameworks.Key Features of the Role:• Involvement in clinical trial and post-marketing safety reporting• Hands-on exposure to adverse event lifecycle management• Opportunity to work with global regulatory authorities and ethics committees• Experience in MedDRA coding and narrative writing• Participation in Quality Management System (QMS) processes• Collaborative cross-functional working environment• Compliance-driven and timeline-sensitive operationsResponsibilities• Assist in processing Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs)• Maintain adverse event tracking systems and ensure accurate documentation• Set up and maintain project files and central documentation records• Report ESRs and PSRs to clients, regulatory authorities, ethics committees, and investigators within study timelines• Log all incoming Adverse Event (AE) and Serious Adverse Event (SAE) reports into departmental tracking systems• Perform accurate data entry of safety information into safety databases• Write detailed and medically accurate patient narratives• Code adverse events using MedDRA terminology where applicable• Assist in listedness assessment against approved product labeling• Generate follow-up queries for missing or inconsistent safety data in consultation with medical teams• Submit expedited SAE reports to clients, regulatory authorities, ethics committees, vendors, and partners within agreed timelines• Support peer and quality review of processed safety reports• Assist in reconciliation of safety databases• Maintain files related to country-specific adverse event reporting requirements• Work in compliance with Standard Operating Procedures (SOPs) and departmental Work Instructions (WIs)• Prepare safety study documentation for archiving at project completion• Coordinate internal and external meetings or teleconferences• Train and mentor PSS assistants or peers as required• Build and maintain strong professional relationships across functional units• Ensure compliance with regulatory requirements and project-specific safety plans• Take responsibility for data accuracy and quality• Provide administrative and operational support to PSS personnel• Perform additional duties as assignedRequired QualificationsCandidates should have an educational background in Life Sciences, Pharmacy, Nursing, Medical Sciences, or related disciplines. Equivalent industry experience may be considered in lieu of formal qualifications. Strong English communication skills (spoken and written) are mandatory, along with proficiency in the local language where applicable.Educational Requirements:• Non-degree qualification with 1–2 years of Safety or relevant industry experience, OR• Associate Degree with 6 months to 1 year of Safety or relevant experience, OR• Bachelor’s Degree (BS/BA) with 0–1 year of Safety or relevant experience, OR• Master’s Degree (MS/MA) with 0–6 months of Safety or relevant experience, OR• PharmD with 0–6 months of Safety experience• A one-year PharmD residency or fellowship may be considered as relevant experiencePreferred disciplines include Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences, or related areas.Experience and Skills:• Experience in processing AE/SAE reports and working with safety databases is preferred• Familiarity with regulatory submissions and reporting timelines• Background in pharmaceutical, biotechnology, or CRO environments is advantageous• Strong attention to detail and commitment to data accuracy• Ability to prioritize tasks and manage multiple responsibilities simultaneously• Good logical reasoning and proofreading skills, especially for numerical data• Proficiency in MS Office and general computer applications• Strong written and verbal communication skills• Ability to work effectively in a team-oriented environment• Good keyboard and documentation management skills• Capability to operate standard office equipmentSalary InsightsThe compensation package is competitive and aligned with industry standards for entry-level to junior pharmacovigilance professionals. Salary may vary depending on qualifications, prior safety experience, technical expertise, and location. Additional benefits may include health coverage, performance incentives, and professional development opportunities.Company OverviewThe organization is a leading Contract Research Organization (CRO) specializing in clinical development and patient safety services. It provides comprehensive pharmacovigilance solutions, regulatory support, and clinical trial management to global pharmaceutical and biotechnology companies. With a strong commitment to regulatory compliance and quality standards, the company supports safe and efficient drug development across therapeutic areas.FAQsQ1. Is prior pharmacovigilance experience mandatory?Prior safety experience is preferred but not mandatory for candidates with relevant educational qualifications.Q2. What is Safety experience?Safety experience includes processing AE/SAE reports, narrative writing, database handling, and regulatory submission exposure.Q3. Is MedDRA knowledge required?Basic understanding of MedDRA coding is beneficial but may be developed during training.Q4. Is this role suitable for fresh graduates?Yes, candidates with 0–1 year of relevant experience may apply based on qualification criteria.Q5. What are the growth opportunities?Employees may progress to Senior Safety Associate, Drug Safety Officer, or Pharmacovigilance Specialist roles.Application Tips• Highlight experience in AE/SAE processing or clinical data management• Mention familiarity with safety databases and MedDRA terminology• Emphasize attention to detail and compliance awareness• Demonstrate understanding of regulatory timelines during interviews• Keep your resume structured, concise, and focused on relevant safety skills• Prepare examples showcasing teamwork and problem-solving abilities

Why This Role MattersThe Medical and Scientific Reviewer ensures that all promotional and non-promotional materials, scientific documents, and medical communications are accurate, scientifically balanced, and compliant with applicable regulations. By reviewing content across multiple therapeutic areas, interpreting scientific literature, and supporting medical affairs and information teams, this role helps clients deliver high-quality, ethical, and scientifically rigorous information to healthcare professionals and patients. The position ensures both regulatory compliance and medical accuracy, contributing directly to patient safety and informed decision-making.Job DescriptionThe Medical and Scientific Reviewer is responsible for reviewing, fact-checking, and approving scientific and medical content for promotional and non-promotional materials. The role involves analyzing literature, preparing scientifically rigorous documents, supporting medical affairs, and ensuring alignment with medical strategies. The reviewer collaborates with internal teams, clients, and medical signatories, maintaining compliance with regulatory requirements and best practices. This position also contributes to SOP creation, process improvements, and content management using platforms like Veeva Vault PromoMats / MedComms.Key Features Of The Role• Review and fact-check promotional and non-promotional materials for medical, legal, and regulatory compliance• Ensure scientific accuracy, clinical and statistical relevance, and balanced presentation of data• Evaluate claims, references, and alignment with approved product labels• Support medical content creation including SRDs, FAQs, slide decks, abstracts, posters, and training materials• Collaborate with internal and client medical signatory reviewers for timely document approval• Use content management tools (e.g., Veeva Vault PromoMats / MedComms) for document upload, referencing, and annotations• Identify, communicate, and resolve issues impacting timelines or content quality• Propose content and process improvements to reduce recurring errors• Participate in client meetings and contribute to strategic discussions on medical communications• Support SOP, template, checklist, and style guide creation and updatesResponsibilities• Conduct thorough scientific review of medical and promotional content across multiple therapeutic areas• Analyze and interpret scientific literature, clinical trials, and regulatory data• Ensure all content is scientifically accurate, contextually correct, and aligned with medical strategy• Review claims for accuracy, relevance, and adequate supporting data• Collaborate with medical, regulatory, and creative teams to resolve findings and approve content• Support medical affairs and medical information teams with content creation and document development• Ensure compliance with US regulations, industry codes of practice, and internal standards• Manage multiple projects and meet deadlines while maintaining high-quality outputs• Flag quality issues proactively and implement corrective or preventive actions• Support cross-functional collaboration across EVERSANA business units and client teamsRequired QualificationsEducational Requirements• PharmD, M.Pharm, MS Pharm, Ph.D., BDS, MDS, or MBBS with relevant experience in scientific writing or reviewingExperience And Skills• Minimum of 2 years of experience in scientific writing, document QC, or medical content review within life sciences or pharmaceuticals• Experience across multiple therapeutic areas including oncology, immunology, rare diseases, and others• Proficient in literature searches and analysis using PubMed, Ovid, Embase, RightFind, etc.• Strong medical and scientific knowledge, with understanding of clinical trials, drug development, and medical terminology• Experience with content management platforms (e.g., Veeva Vault PromoMats / MedComms)• Excellent communication, editing, and project management skills• High attention to detail, analytical thinking, and ability to translate complex data for different audiences• Knowledge of US regulations and best practices for medical communications and promotional materials• Ability to work independently and collaboratively in a matrix team environmentSalary Insights• Compensation as per company norms and industry standards• Opportunities to work remotely and exposure to global medical communications projects• Career growth in medical affairs, regulatory, and scientific communicationsCompany OverviewEVERSANA is a global life sciences services provider, supporting more than 650 clients with commercialization, medical, regulatory, and scientific services. The company emphasizes diversity, inclusion, and professional development while delivering high-quality medical content to improve patient outcomes. EVERSANA values integrity, collaboration, and scientific excellence across all therapeutic areas.FAQsQ: What type of materials will I review?A: Promotional and non-promotional materials, scientific responses, FAQs, slide sets, abstracts, posters, and medical training materials.Q: Will I interact with clients?A: Yes, the role involves collaboration with internal teams, medical signatory reviewers, and client representatives.Q: What tools are used for content management?A: Veeva Vault PromoMats, MedComms, Microsoft Office, Acrobat, and other content management platforms.Application Tips• Highlight experience in medical or scientific content review across therapeutic areas• Emphasize familiarity with regulatory requirements and industry best practices• Showcase expertise in literature analysis, scientific writing, and document QC• Demonstrate project management, attention to detail, and collaborative skills

Why This Role MattersMedical writing plays a central role in translating complex clinical and scientific data into clear, compliant, and impactful communication for healthcare professionals, regulators, and patients. As a Senior Medical Writer at Syneos Health, you will directly support global pharmaceutical and biotech organizations by developing scientifically accurate and regulatory-compliant content. This role contributes to accelerating therapy delivery, enhancing scientific communication quality, and ensuring patient-centric information dissemination. Through high-quality medical information writing, this position strengthens evidence-based decision-making across clinical, regulatory, and medical affairs functions.Job DescriptionThe Senior Medical Writer will serve as a lead contributor on medical information writing projects, supporting global standard scientific response documents, FAQs, guidance materials, manuscripts, and publication deliverables. The role requires coordination with cross-functional teams including data management, regulatory affairs, biostatistics, and medical affairs. The candidate will respond to escalated scientific queries from healthcare professionals and internal stakeholders while ensuring adherence to journal, congress, and company regulatory standards. The position demands scientific accuracy, attention to detail, leadership in mentoring junior writers, and familiarity with literature search and publication planning tools.Key Features of the Role:• Remote full-time opportunity• Leadership role within medical writing function• Exposure to global publication and medical information projects• Cross-functional collaboration with regulatory and clinical teams• Opportunity to mentor junior medical writers• Involvement in scientific figure development and publication planningResponsibilities• Lead assigned medical information writing projects• Mentor and guide less experienced medical writers• Develop and update global scientific response communications (gSSRCs)• Respond to escalated scientific queries from HCPs and stakeholders• Conduct literature searches using PubMed and client databases• Develop manuscripts, abstracts, posters, and oral presentations• Ensure adherence to regulatory and journal guidelines• Review documents for scientific accuracy and referencing quality• Coordinate with regulatory, medical affairs, and biostatistics teams• Support publication planning using tools such as Datavision and PubConnect• Create scientific figures using GraphPad Prism and Adobe Illustrator• Maintain compliance with SOPs and client templates• Monitor project timelines and budget specifications• Serve as peer reviewer for internal document quality checksRequired Qualifications• Strong experience in medical information writing or publication writing• Familiarity with regulatory standards and journal guidelines• Experience handling scientific documentation and literature analysis• Ability to work independently with minimal supervision• Strong project management capabilitiesEducational Requirements:• Advanced degree in Life Sciences, Pharmacy, Medicine, Biotechnology, or related discipline preferred• Equivalent relevant experience consideredExperience and Skills:• Experience in clinical manuscript and publication development• Strong scientific writing and editing expertise• Familiarity with figure creation and data visualization tools• Knowledge of publication planning platforms• Excellent analytical and literature review skills• Strong communication and stakeholder coordination skills• Attention to detail and high-quality documentation standards• Ability to work within budget and timeline constraints• Leadership and mentoring capabilitiesAge Eligibility:No specific age criteria mentioned. Candidates must meet educational and professional qualification requirements.Salary InsightsCompensation is competitive and aligned with industry standards for senior medical writing roles. Salary may vary based on experience, therapeutic expertise, and project leadership exposure. Additional benefits may include career progression programs, training opportunities, and performance incentives.Company OverviewSyneos Health is a fully integrated biopharmaceutical solutions organization operating in over 110 countries with approximately 29,000 employees globally. The organization accelerates clinical development, medical affairs, and commercialization strategies for pharmaceutical and biotech clients. Known for its patient-centric Clinical Development model, Syneos Health supports the majority of recently approved FDA and EMA products. The company promotes diversity, professional growth, and a collaborative culture under its “Work Here Matters Everywhere” philosophy.FAQsIs prior medical writing experience required?Yes, senior-level experience in medical writing is expected.Is the role fully remote?Yes, this position is remote-based in Pune/Pimpri-Chinchwad Area.Does the role involve travel?Minimal travel may be required (less than 25%).What type of documents will be handled?Medical information documents, manuscripts, abstracts, posters, and scientific responses.Are regulatory guidelines important for this role?Yes, adherence to journal, regulatory, and SOP standards is critical.Application Tips• Highlight publication and medical information writing experience clearly• Showcase manuscript, abstract, and scientific communication exposure• Mention familiarity with PubMed, regulatory guidelines, and figure tools• Quantify project leadership or mentoring experience• Emphasize compliance, accuracy, and document quality standards• Tailor your resume to highlight therapeutic area expertise and writing portfolio

Role & Responsibilities• Perform primary medical review of safety cases including assessment of seriousness, listedness/labeling, causality, adverse event coding, and narrative review• Update and document daily case data and feedback in tracking tools to ensure workflow management• Take full responsibility for assigned deliverables in line with quality, compliance, productivity SLAs, and KPIs• Provide medical training and guidance to case processing teams after completion of one year of tenure• Support aggregate reporting and signal detection activities related to single case processing• Maintain high standards of customer service and compliance cultureQualification• Bachelor’s degree in Medical Science or MD or DO or equivalent qualification• Fortrea may consider relevant equivalent experience in lieu of formal education• English proficiency – Speaking (ILR Level 3+), Writing/Reading (ILR Level 4+)Experience• Working knowledge of medical sciences, diagnosis, therapeutics, drug treatments, and procedures• Knowledge of regulatory requirements for Clinical Research• Understanding of ICH-GCP guidelines• 1–2 years of clinical practice experience preferredSkills• Medical safety and pharmacovigilance knowledge• Clinical case assessment and causality evaluation• Understanding of regulatory compliance and post-marketing surveillance• Strong documentation and analytical skills• Ability to work in office or home-based environmentAbout the CompanyFortrea is a global contract research organization (CRO) providing clinical development and post-marketing services to pharmaceutical, biotechnology, and medical device companies. The organization focuses on delivering high-quality clinical research, pharmacovigilance, and regulatory support services to improve patient safety and accelerate drug development worldwide.

Roles & Responsibilities• Lead drafting, editing, and submission of manuscripts arising from clinical, surgical, and genetics research• Coordinate journal submissions, revisions, and responses to peer reviewers• Ensure adherence to ethical standards, reporting guidelines, and journal requirements• Contribute to review articles, commentaries, and perspective papers aligned with institutional priorities• Prepare high-quality PowerPoint presentations for conferences, workshops, and academic forums• Support faculty and trainees in developing abstracts, posters, and oral presentations• Translate research outputs into educational and capacity-building materials• Manage the editorial workflow of the in-house journal from manuscript receipt to final decision• Coordinate peer-review process including reviewer identification, invitations, follow-ups, and timelines• Conduct editorial quality checks, plagiarism screening, and ensure compliance with publication standards• Maintain records of submissions, reviews, decisions, and publication schedules• Mentor trainees, interns, and junior staff in scientific writing and research communication• Support workshops, conferences, webinars, and capacity-building initiatives conducted at the centreQualification• MBBS or BHMS or MS in Life Sciences / Biomedical Sciences / Genetics or related disciplineExperience• Minimum 5 years of experience in medical or clinical writing• Demonstrated experience in manuscript writing and publication in peer-reviewed journals• Experience in preparing conference abstracts, posters, and scientific presentations• Prior exposure to clinical research and multidisciplinary collaboration desirableSkills• Strong scientific writing and publication strategy expertise• Knowledge of clinical research methodologies and translational oncology• Excellent editing, proofreading, and analytical skills• Ability to manage editorial workflows and peer-review coordination• Strong communication and collaboration skills• Understanding of ethical publication standards and plagiarism screeningAbout The CompanyPrashanti Cancer Care Mission is a research-focused institution based in Pune, India, dedicated to advancing breast disease research, cancer genetics, and translational oncology. The centre emphasizes high-quality scientific communication, publication excellence, and capacity-building initiatives to support academic growth and multidisciplinary collaboration in oncology research.

Role & Responsibilities• Review biomedical literature for adverse reaction reports (ICSR/Non-ICSR)• Perform relevancy assessments and MedDRA coding• Draft high-quality medical narratives• Mentor scanning teams on inclusion/exclusion criteriaQualification• MBBS/MD (MCI Registered / FMGE cleared)Experience• 1–3 years in Pharmacovigilance (Mandatory)Skills• Strong understanding of pharmacovigilance and drug safety processes• Proficiency in MedDRA coding and adverse event reporting• Excellent medical writing and narrative drafting skills• Ability to mentor and guide team members• Strong attention to detail and data accuracyAbout the CompanyOur client is a global player in the pharmaceutical and healthcare space, committed to ensuring the safety of medicines and protecting patient health through robust pharmacovigilance practices. As a Medical Reviewer in their team, you will have an opportunity to impact drug safety strategies in a fast-paced and dynamic environment.

Roles & Responsibilities• Perform quality review of safety cases, regulatory documents, and pharmacovigilance reports• Compile quality metrics, identify trends, and support client quality reviews• Assist in CAPA preparation, implementation, and effectiveness monitoring• Review adverse events, product quality complaints, and medical information cases within timelines• Support audit readiness, regulatory inspections, and quality management activities• Conduct data analysis and contribute to process improvement initiatives• Assist in training coordination, documentation review, and QC activities• Support reconciliation of safety data and regulatory documentation complianceQualification• Bachelor’s / Master’s / PhD in Medicine, Pharmaceutical Sciences, Life Sciences, Nursing, or related disciplineExperience• Minimum 2+ years of experience in Pharmaceutical, Biotechnology, or CRO industry• Experience in Pharmacovigilance, Safety Writing, or Quality Review preferredSkills• Knowledge of Pharmacovigilance processes and safety reporting requirements• Understanding of GCP, GVP, ICH, EU, and FDA regulatory guidelines• Strong attention to detail and documentation review skills• Good analytical, communication, and problem-solving abilities• Proficiency in MS Office and safety data management toolsAbout the OrganizationFortrea is a global Contract Research Organization (CRO) providing clinical development, pharmacovigilance, and regulatory support services. The company partners with life sciences organizations to deliver high-quality, compliant solutions that improve patient safety and accelerate drug development.

Roles & Responsibilities• Perform scientific fact-checking and medical review of promotional and non-promotional materials• Ensure clinical, statistical, and scientific accuracy of claims and references• Verify alignment of content with approved product labeling and medical strategy• Review and proofread medical content against source references• Collaborate with Medical, Legal, and Regulatory (MLR) review teams• Work within Veeva Vault PromoMats / MedComms platforms• Support development of SRDs, FAQs, slide decks, abstracts, posters, and training materials• Conduct literature searches using PubMed, Embase, Ovid, RightFind, etc.• Identify quality issues and recommend corrective and preventive actions (CAPA)• Participate in client meetings and cross-functional discussionsQualification• PharmD / M.Pharm / M.S. Pharm• PhD / MBBS / BDS / MDSExperience• Minimum 2 years of experience in scientific writing, document QC, or medical review• Exposure to medical affairs, medical information, or medical communications preferredSkills• Strong understanding of clinical trials and drug development• Knowledge of US pharmaceutical promotional regulations• Experience with Veeva Vault MedComms or PromoMats (preferred)• Excellent written and verbal communication skills• Ability to review content across multiple therapeutic areasAbout the OrganisationEVERSANA is a leading global life sciences services company providing integrated commercialization, medical affairs, regulatory, and market access solutions, supporting biopharma companies in delivering therapies to patients worldwide.

Role & Responsibilities• Provide first aid and OPD-style consultations for students and staff at the campus first aid room• Coordinate emergency care and health sessions as required• Be available on-call post-duty hours for urgent cases• Ensure healthcare protocols are followed at the campus• Work in a self-sufficient 28-acre campus featuring hostels, labs, and Wi-FiSkills• Strong knowledge of physiology• Patient care expertise• Basic life support skills• Clinical experience in a similar settingQualifications• MBBS degree with valid MCI registration• Minimum 2 years of clinical experience• Female candidates preferred• Immediate joiners prioritizedBenefits• Free on-campus accommodation abiding by college rules• Food allowance• Competitive salary• Health insurance• Life insurance• Cell phone reimbursement• Flexible scheduleAbout The Company• Apollo Shine Foundation is a reputed healthcare organization that provides medical services in academic settings.

Roles & Responsibilities • Manage end-to-end scientific writing and publication workflows using Pub Connect. • Create and maintain publication plans, author approvals, versions and checklists. • Coordinate journal and congress submissions including pre-submission inquiries and dummy submissions. • Track submission requirements, guideline updates and provide status updates to stakeholders. • Prepare and collate metadata and complete submission packages. • Ensure accurate documentation from kick-off through review, sign-off and approvals. • Support system activities such as uploads, reference linking and workflow monitoring. • Ensure compliance with journal/congress guidelines, SOPs, client standards and templates. • Perform literature searches and provide ad-hoc operational support as required. • Manage assigned tasks within budgeted hours and defined timelines. Qualification • Master’s degree in Life Sciences, Pharmacy, Medicine or related discipline. Experience • Relevant experience as a Medical Writer or Publication Project Coordinator in a medical communications or biopharmaceutical environment. Skills • Strong experience in scientific writing and publication planning. • Hands-on knowledge of Pub Connect and publication planning tools such as Datavision, Veeva Vault PromoMats or MedComms systems. • Understanding of journal and congress submission processes and regulatory guidelines. • Strong documentation, organizational and project management skills. • Ability to manage multiple workflows and coordinate with cross-functional and sponsor teams. • Strong communication and stakeholder management skills. About the Company Syneos Health® is a leading fully integrated biopharmaceutical solutions organization supporting clinical development, medical affairs and commercial functions worldwide, partnering with global life sciences companies to accelerate the delivery of therapies through innovation, collaboration and a people-centric culture.

Roles & Responsibilities • Assist in regulatory documentation and compliance-related activities • Support preparation, review, and maintenance of regulatory submissions • Gain hands-on exposure to regulatory processes under expert guidance • Coordinate with internal teams for data collection and documentation • Support ongoing regulatory projects and new initiatives • Follow company SOPs and regulatory guidelines Qualifications • B.Pharm / M.Pharm / MD / BDS / BAMS / BHMS Skills • Strong interest in Regulatory Affairs • Good communication and documentation skills • Fluency in English, Hindi, and Marathi • Willingness to learn and adapt in a professional environment Additional Details • Working Days: Monday to Friday • Travel Allowance provided • Opportunity for payroll absorption for high-performing interns About the Organisation Agenome Research is a research-driven organization offering practical, real-world exposure in regulatory affairs, focused on developing skilled professionals through hands-on training and expert mentorship.

Roles & Responsibilities: • Develop, program, and validate ADaM datasets as per CDISC standards. • Create Tables, Listings, and Figures (TLFs) using SAS and/or R. • Implement Statistical Analysis Plans (SAP) and Statistical Programming Plans (SPP). • Ensure compliance with regulatory and industry standards (CDISC – SDTM, ADaM). • Collaborate closely with biostatisticians and clinical teams to ensure data accuracy. • Develop reusable macros and automate programming processes for efficiency. • Perform independent QC checks on statistical outputs and deliverables. • Support programming activities across multiple therapeutic areas including Oncology, Neuroscience, and Immunology. Qualifications • Graduate / Postgraduate in Life Sciences, Engineering, Statistics, or related disciplines.Experience: • 3 to 12 years of experience in clinical or biostatistical programming. • Hands-on experience in ADaM, TLF development, and clinical trial data analysis. Skills: • Strong expertise in SAS and/or R programming. • In-depth knowledge of CDISC standards (SDTM, ADaM). • Experience working with clinical trial protocols and regulatory guidelines. • Proficiency in TLF generation and data manipulation techniques. • Strong analytical, problem-solving, and attention-to-detail skills. • Exposure to additional tools such as Python or SQL (preferred). • Basic understanding of machine learning concepts applied to clinical data (preferred). About the Organisation: The organization is a leading clinical research and data analytics-driven company supporting global clinical trials across multiple therapeutic areas, offering a collaborative work environment, exposure to regulatory-compliant projects, and long-term career growth opportunities in statistical and clinical programming.