Doctor Jobs

Role & Responsibilities • Perform medical review of Individual Case Safety Reports (ICSRs) • Conduct signal detection and interpret emerging safety trends • Develop and review aggregate safety reports including PSURs, PBRERs and DSURs • Support benefit–risk assessments and safety strategy discussions • Ensure compliance with global pharmacovigilance regulations (ICH, EMA, US FDA) • Provide medical evaluation of case narratives and literature reports • Collaborate with cross-functional safety and quality teams • Contribute to clinical risk management and regulatory safety activities Qualification • MBBS / MD (Registered Medical Practitioner in India) Experience • Minimum 1+ year experience in Pharmacovigilance / Drug Safety Skills • Signal detection & aggregate reporting • ICSR medical review • Global PV regulatory knowledge • Analytical thinking & medical interpretation • Strong written and verbal communication About the Company • OrciMed Life Sciences is a pharmacovigilance and drug safety organization providing global safety services, signal detection, aggregate reporting and regulatory compliance solutions to pharmaceutical companies

Role & Responsibilities • Manage safety reconciliation and compliance monitoring activities for global clients • Perform reconciliation of Reference Safety Information (RSI) for assigned products • Conduct data mining and review of FDA Adverse Event Reporting System (FAERS) and other regulatory safety databases • Edit, review, and reconcile consolidated global product lists • Manage global exchange of safety information related to product approvals, launches, cancellations, and RSI updates • Maintain and update all documents related to safety reconciliation and compliance activities • Ensure adherence to global pharmacovigilance regulations and internal SOPs Qualification • B.Pharm / M.Pharm Experience • 5–8 years of experience in the Pharmacovigilance domain • Hands-on experience in safety reconciliation and compliance monitoring Skills • Pharmacovigilance compliance & reconciliation • FAERS database review • Reference Safety Information (RSI) management • Advanced MS Excel skills • Mailbox management & documentation • Strong analytical and communication skills About the Company • A global life sciences organization providing pharmacovigilance, regulatory, and compliance services across international markets

Role & Responsibilities • Initiate communication with internal business teams and subsidiaries for SDEA requirements • Follow up with third-party partners to establish and maintain SDEAs • Perform timely exchange of safety data with business partners • Conduct adverse event reconciliation with partners • Support case processing and safety writing activities • Ensure compliance with global pharmacovigilance standards • Stay updated with current PV regulations and scientific developments Qualification • B.Pharm / M.Pharm / BAMS / BHMS Experience • 3–4 years of experience in pharmacovigilance • Hands-on experience in case processing, safety writing and SDEA management • Experience in safety data exchange and reconciliation activities Skills • Knowledge of global pharmacovigilance regulations • SDEA management & reconciliation • Case processing & safety writing • Strong written and verbal communication skills • Presentation & documentation skills About the Company • A leading life sciences organization engaged in delivering high-quality pharmacovigilance and drug safety solutions across global markets

Role & Responsibilities • Manage HEOR project portfolios aligned with HORPs • Drive integrated budget planning and quarterly forecasting • Track milestones, timelines, scope and compliance • Coordinate cross-functional HEOR execution • Support contracting, procurement and sourcing activities • Facilitate change control and risk mitigation • Provide leadership updates and portfolio reporting • Represent HEOR in critical chain planning • Lead retrospectives and process improvements Qualification • Bachelor’s / Master’s in Pharmacy, Life Sciences, Science OR MBA Experience • 7–10 years in Pharma / HEOR / RWE / Clinical Project Management Skills • Portfolio & program management • Budgeting and forecasting • Stakeholder coordination • Risk & change management • MS Word, Excel, PowerPoint, MS Project • Strong analytical & communication skills About the Company • Eli Lilly and Company is a global healthcare leader delivering life-changing medicines and advancing patient access worldwide

Role & Responsibilities Maintain deep scientific and disease area expertise within Neurosciences Engage in continuous scientific learning to stay updated on disease states, Lilly and competitor products Conduct high-quality, field-based scientific engagements with Key Opinion Leaders and scientific experts Provide accurate, balanced, and unbiased medical and scientific information to healthcare professionals Identify collaborative research opportunities and connect external experts with Lilly internal stakeholders Capture, synthesize and communicate strategic medical insights to cross-functional internal teams Support affiliate medical planning and contribute to medical strategy development Develop and implement strategic territory plans and manage regional priorities effectively Ensure compliance with internal policies, regulatory guidelines and ethical standards Support medical education initiatives and scientific exchange programs Qualification MBBS / MD / PhD in Health Sciences or medically related field Experience Prior experience as an MSL or field-based medical affairs professional preferred Experience engaging with Key Opinion Leaders and scientific experts in Neurosciences highly desirable Skills Neuroscience therapeutic area knowledge Medical affairs and scientific communication Strategic planning and territory management KOL engagement and professional networking Advanced presentation and communication skills Strong analytical, critical thinking and problem-solving ability High emotional intelligence and interpersonal skills Willingness to travel extensively (up to 80%) About the Company Eli Lilly and Company is a global healthcare leader dedicated to discovering and delivering life-changing medicines, improving disease understanding and patient outcomes, and contributing to communities worldwide through science-driven innovation and compassionate healthcare solutions.

Role & Responsibilities Conduct detailed medical review and assessment of Individual Case Safety Reports (ICSRs) in safety databases Ensure accurate selection and coding of adverse events as per MedDRA guidelines Assess seriousness, expectedness, listedness and causality of reported cases Review suspect and concomitant medications, laboratory data, medical history and case narratives Prepare and provide Company Clinical Comments and medical narratives Ensure compliance with Good Pharmacovigilance Practices (GVP), Good Clinical Practice (GCP) and ICH guidelines Implement EMA and global regulatory requirements in safety reporting processes Maintain high quality and accuracy in safety case assessments Support audits, inspections and continuous quality improvement initiatives Qualification MBBS / MD or equivalent medical degree Experience Minimum 5–8 years of experience in Pharmacovigilance / Drug Safety / Medical Review roles Skills ICSR medical review and causality assessment MedDRA coding and narrative writing Strong knowledge of GVP, GCP, ICH and EMA guidelines Safety database handling (ARGUS, ARISg, etc.) Analytical skills and medical judgement Excellent documentation and communication skills About the Company The organization is a global pharmacovigilance and clinical research service provider delivering comprehensive drug safety, regulatory and clinical operations solutions to pharmaceutical and biotechnology companies worldwide, with a strong commitment to patient safety and regulatory compliance.

Role & Responsibilities Plan, coordinate and oversee Phase III & IV human clinical trials Support implementation of clinical protocols and completion of final study reports Recruit clinical investigators and negotiate study design and budgets Coordinate investigator site initiations and multi-center studies Monitor protocol adherence and determine study completion Coordinate regulatory submissions and reporting to health authorities Participate in adverse event reporting and safety monitoring activities Collect, analyze and manage clinical research data Act as liaison with partner organizations under licensing or collaboration agreements Support clinical research planning and execution activities Qualification Associate Degree (or higher) in Life Sciences, Pharmacy, Nursing, Clinical Research or related discipline Experience Minimum 1 year of experience in Clinical Research / Medical Affairs / Clinical Trials Skills Clinical trial coordination Protocol compliance & monitoring Regulatory documentation and reporting Safety reporting knowledge Data collection & documentation Stakeholder coordination Basic project management skills About the Company A leading global healthcare organization engaged in advanced clinical research, medical affairs and post-marketing clinical development to support safe and effective therapeutic innovations.

Role & Responsibilities Build and maintain relationships with KOLs and HCPs in medical genetics, genomics, oncology, reproductive medicine and related specialties Present scientific and clinical data for genetics-based diagnostic products Act as primary scientific contact for product-related medical inquiries Support advisory boards, conferences, CMEs, and scientific symposia Deliver scientific training for internal sales, marketing and support teams Conduct educational programs and academic presentations for clinicians Support clinical trials, real-world evidence and post-marketing studies Provide test interpretation support and genotype-phenotype correlation guidance Collect medical insights from the field to support product and marketing strategy Ensure compliance with ethical, legal and regulatory standards Qualification PhD or MD in Medical Genetics, Molecular Biology, Genomics or related discipline Experience Relevant experience in medical affairs, clinical genetics, genomics or scientific liaison roles preferred Skills Scientific communication and presentation Clinical genomics knowledge KOL engagement and stakeholder management Strategic planning and insight generation Cross-functional collaboration Willingness to travel Pan-India About the Company HaystackAnalytics is a HealthTech genomics company backed by DST, BIRAC and DBT, developing advanced diagnostic solutions in infectious diseases and clinical genomics, including nationally recognized innovations in tuberculosis and personalized diagnostics.

Role & Responsibilities Provide outpatient and basic inpatient medical care to ECHS beneficiaries Examine patients, diagnose medical conditions, and prescribe appropriate treatment Maintain accurate medical records and treatment documentation Refer patients to specialists or higher centres when required Ensure adherence to clinical protocols and ECHS healthcare guidelines Participate in medical audits, health camps, and awareness programs as assigned Support emergency care and first-line medical interventionsName of the PostsNo.of VacanciesQualificationMedical Officer 02MBBS Experience Freshers and experienced MBBS doctors may apply Skills Clinical diagnosis and patient management Prescription and documentation accuracy Emergency medical handling Good communication and interpersonal skills Knowledge of government healthcare systems preferred About the Company The Ex-Servicemen Contributory Health Scheme (ECHS) is a Government of India healthcare initiative that provides comprehensive medical care to ex-servicemen and their dependents through a nationwide network of polyclinics and empanelled hospitals.Last Date of Application27-01-2026Official NotificationClick Here

Role & Responsibilities Lead product registrations and regulatory submissions including preparation of complex and routine filing packages Coordinate documentation, monitor timelines, and manage regulatory project activities Prepare responses to health authority deficiency letters Represent Regulatory CMC in cross-functional project meetings Monitor regulatory timelines and identify risks impacting project progression Maintain coordination with regional and affiliate regulatory teams Assess and approve lifecycle change requests and ensure ongoing compliance Develop Regulatory CMC strategies for assigned products and projects Identify and mitigate regulatory risks across product life-cycle Attend health authority meetings and provide licensing due diligence support Support process improvements, position papers, and regulatory work aids Maintain technical and regulatory knowledge of global and regional CMC requirements Qualification Bachelor’s degree in Pharmacy, Biology, Chemistry, Pharmacology, or related discipline Experience Minimum 10 years in Regulatory Affairs, R&D, Manufacturing, or related regulatory functions Skills Regulatory CMC strategy development Product registrations and lifecycle management Health authority interaction Risk management and compliance Cross-functional coordination Strong project management skills Technical regulatory documentation expertise Leadership, mentoring, and stakeholder management About the Company The organization is a global life sciences company engaged in pharmaceutical development and manufacturing, supporting worldwide regulatory compliance, product registration, and lifecycle management to deliver high-quality medicines to patients globally.

Role & Responsibilities Perform medical assessment of Individual Case Safety Reports (ICSRs) in the safety database Conduct medical evaluation of serious and non-serious adverse event cases Assess quality of vendor medical assessments against defined KPIs Issue follow-up medical queries and ensure completeness of case information Maintain medical knowledge of product safety profiles across therapeutic areas Monitor case workflows to ensure timely processing and compliance Collaborate with Medical Safety and Pharmacovigilance teams Support audits, regulatory inspections, and internal trainings Contribute to pharmacovigilance activities for clinical and post-marketing products Qualification MBBS or MD Experience Minimum 3 years in pharmaceutical or biotech industry At least 2 years in pharmacovigilance / patient safety Minimum 2 years of hospital or private clinical practice Skills ICSR medical review Pharmacovigilance compliance Medical query management Clinical judgment and safety evaluation Strong communication and teamwork skills Ability to work in a global, fast-paced environment About the Company The organization is a global science and technology leader delivering innovative solutions in healthcare, life sciences, and electronics, with a strong commitment to improving and prolonging patient lives across oncology, neurology, and fertility therapeutic areas.

Role & Responsibilities Conduct detailed patient history and clinical examination Diagnose medical conditions and prescribe homeopathic treatment Develop personalized treatment plans and monitor patient progress Provide follow-up consultations and continuity of care Maintain accurate medical records and documentation Counsel patients on lifestyle modification, diet and preventive healthcare Conduct health awareness programs, workshops and seminars Represent the organization in medical events and conferences Ensure ethical and professional medical practice Supervise and guide junior staff or interns when required Qualification MBBS or BAMS from a recognized institution Experience Freshers or experienced candidates can apply Skills Clinical assessment and diagnosis Patient counselling Good communication skills Documentation and reporting Knowledge of homeopathic principles Ethical medical practice About the Company The organization provides holistic healthcare services focused on preventive medicine, patient education, and community health development through structured clinical care and awareness initiatives.

Role & Responsibilities • Prepare and review clinical study outlines, feasibility synopses, and clinical trial protocols (Phase I–IV, BA/BE) • Author and review Clinical Study Reports (CSRs) for regulatory submissions • Prepare Common Technical Documents (CTDs) and subject-facing documents (ICD, IBs, diaries, etc.) • Draft and review SAE narratives and regulatory submission documents (IND, NDA, BLA, MAA, 505(b)(2), biosimilar, hybrid applications) • Develop Module 2.4, 2.5, 2.6, 2.7 summaries, Clinical/Non-clinical Overviews, ISS/ISE, and briefing documents • Draft Pre-IND, Pre-NDA, SAM, orphan drug designation and expedited approval packages • Support cross-functional teams with SAPs, TLFs, eCRF outlines and study-specific documentation • Manage medical writing activities across studies and departments with minimal supervision • Ensure compliance with internal SOPs and global regulatory guidelines • Prepare and maintain departmental SOPs and quality documentation • Collaborate with Biostatistics, Data Management, Regulatory Affairs, and Medical Leads • Manage departmental administrative requirements and additional tasks as assigned Qualification PhD / MBBS / MD / M.Pharm / Pharm.D Experience Minimum 5 years of professional regulatory medical writing experience Skills • Expert knowledge of regulatory guidelines and submission requirements • Strong proficiency in MS Word, PowerPoint, Excel, and Adobe Acrobat/PDF editors • Understanding of publication processes and congress activities • Excellent interpersonal and communication skills • High attention to detail and scientific writing excellence • Strong multitasking, prioritization, and teamwork abilities About the Company A growing clinical research organization delivering high-quality regulatory medical writing, clinical documentation, and submission support services to global pharmaceutical and biotechnology clients

Role & Responsibilities • Execute Medical Affairs plan for AbbVie Oncology portfolio in India • Develop and maintain relationships with key opinion leaders, academic centers, and researchers • Provide scientific education and balanced medical information to healthcare professionals • Organize and support advisory boards, round tables, and scientific meetings • Present clinical and scientific data on AbbVie oncology products • Support clinical trials, research initiatives, and medical education programs • Serve as internal scientific resource for disease-state and product communications • Deliver ongoing training to medical affairs, sales, and cross-functional teams • Ensure compliance with regulatory, ethical, and company requirements • Maintain accurate documentation and manage activities within assigned budgets • Collaborate closely with Commercial, Medical Affairs, and R&D teams • Support HEOR, PV, and global medical office–related functions • High field engagement (approx. 60% travel) across assigned territories Qualification MD or MBBS Experience Minimum 2–3 years post-qualification experience in Medical Affairs Pharma industry or clinical research experience preferred Skills • Strong scientific communication and presentation skills • Ability to interpret and communicate clinical data effectively • Relationship building and stakeholder engagement • Cross-functional collaboration in matrix environments • Analytical thinking and problem-solving • Proficiency in MS Office tools About the Company AbbVie is a global biopharmaceutical leader focused on discovering and delivering innovative medicines across immunology, oncology, neuroscience, and eye care, with a strong commitment to improving patient outcomes worldwide

Key Responsibilities • Oversee adherence to Quality Management Framework procedures to ensure delivery of high-quality pharmacovigilance cases • Review and improve project Quality Management Systems and suggest process enhancements • Collaborate with Team Leads, Trainers and Medical Reviewers to implement new or enhanced quality processes • Coordinate with Quality Reviewers to maintain compliance with quality standards • Review late logs, perform Root Cause Analysis (RCA) and define Corrective and Preventive Actions (CAPA) • Ensure timely documentation and closure of late logs as per client SOPs • Conduct training, refresher sessions and awareness programs on case processing conventions • Work with Operational Excellence and Capability Development teams to enhance engagement quality • Support audits, inspections, SOP development and maintenance • Review safety case data for completeness and accuracy • Track, submit and distribute quality and compliance reports • Maintain client mailboxes, SharePoint, databases and safety tools • Drive zero quality deviations leading to regulatory submission delays • Support transitions, documentation archiving, and cross-functional coordination Skills & Competencies • Working knowledge of ICH, GCP, FDA, MHRA and global PV regulations • Strong attention to detail and data accuracy • Good understanding of medical terminology • Strong verbal and written communication skills • Proficiency in MS Excel, Word and PowerPoint • Strong interpersonal and stakeholder management skillsAbout Accenture Accenture is a global professional services company delivering Strategy & Consulting, Technology and Operations services across more than 120 countries. With industry-leading capabilities in digital, cloud and security, Accenture supports global life sciences clients through advanced technology and intelligent operations centers.

Role & Responsibilities • Oversee ICSR medical review activities performed by Global Service Providers (GSP) • Perform quality checks on medical review deliverables for regulatory and company compliance • Review listedness/expectedness and causality assessments • Lead training and competency development for medical reviewers • Act as liaison between SERM, ICSR processing teams and medical review vendors • Monitor KPIs, identify gaps, drive CAPA and continuous improvement initiatives • Support audit readiness, inspections, and regulatory compliance activities • Provide medical guidance on complex and high-risk safety cases • Support local operating companies on medical review processes when required Qualification • Advanced clinical degree preferred (MD / PharmD / Postgraduate Medical Qualification) Experience • 9–12 years of pharmacovigilance medical review experience Skills • Strong expertise in ICSR medical review, causality & listedness assessment • In-depth knowledge of MedDRA coding conventions • Expertise in quality management, KPI monitoring, and CAPA management • Strong understanding of global PV regulations and drug approval processes • Excellent medical judgment, analytical thinking, and communication skills • Leadership ability and stakeholder management in matrix environments • Experience with audits, inspections, CRO/vendor oversight About the Company GSK is a leading global biopharmaceutical company focused on vaccines and specialty medicines across respiratory, immunology, oncology, HIV and infectious diseases. With a mission to positively impact 2.5+ billion people by 2030, GSK unites science, technology and talent to deliver innovative, high-quality, patient-focused healthcare solutions worldwide.

Role & Responsibilities • Support consultants in Medical, Radiation, and Surgical Oncology services • Manage day-to-day inpatient care, ward rounds, and clinical documentation • Coordinate chemotherapy administration, patient admissions, and discharges • Ensure adherence to oncology treatment protocols, safety standards, and quality norms • Act as first point of clinical escalation for oncology patients • Liaise with nursing, pharmacy, and diagnostic teams to ensure smooth patient flow Qualification • MBBS Experience • Relevant clinical experience in Oncology preferred Skills • Strong clinical judgment and patient-centric care approach • Ability to work in high-acuity, multidisciplinary oncology environments • Good communication, coordination, and documentation skills • Knowledge of oncology protocols and patient safety standards About the Company The organization is a rapidly expanding oncology healthcare platform committed to delivering structured, advanced cancer care through multidisciplinary clinical systems, senior oncology leadership, and a collaborative work culture focused on quality and patient safety.

Role & Responsibilities • Perform medical review of clinical, solicited, spontaneous, and literature safety cases • Conduct medical assessment including seriousness, expectedness, labeling, and causality evaluation • Review and validate AE/SAE terms, suspect drugs, concomitant medications, lab data, and medical history • Ensure accurate narrative review and global coding consistency • Develop and maintain strong knowledge of disease biology and key safety concerns for marketed and investigational products • Ensure compliance with global regulatory requirements and internal SOP timelines Qualification • MBBS or equivalent medical qualification Experience • Experience in pharmacovigilance / medical review domain preferred Skills • Strong knowledge of PV regulations and safety case processing • Medical assessment and causality evaluation expertise • MedDRA coding and narrative review skills • High attention to detail and regulatory compliance awareness • Good communication and documentation skills About the Company TCS (Tata Consultancy Services) is a global IT services and consulting leader with a strong Life Sciences practice supporting pharmaceutical and healthcare organizations worldwide through advanced technology, analytics, and compliance-driven solutions.

Role & Responsibilities • Lead medical monitoring of clinical trials, providing safety and efficacy oversight throughout the study lifecycle • Evaluate and review adverse events, serious adverse events (SAEs), and expedited safety reports • Review SAE narratives, IND/IDE safety reports, CIOMS, DSURs, and other aggregate safety reports • Review and approve MedDRA and WHO Drug coding • Provide medical input for protocol development, inclusion/exclusion criteria, and halting rules • Support development of Safety Monitoring Plans, Medical Monitoring Plans, and training materials • Participate in safety oversight committees (DSMB/DMC/SMC) and sponsor/investigator meetings • Support preparation of safety sections for annual reports and clinical study reports • Act as internal medical consultant for feasibility strategies, bid support, and medical training • Contribute to audits, SOP development, quality assurance, and corporate safety activities Qualification • Medical degree (MD / MBBS / MBBCh or equivalent) Experience • Minimum 2 years in clinical practice, pharmaceutical medicine, clinical research, pharmacovigilance, medical affairs, or regulatory domains Skills • Strong clinical judgment and safety monitoring expertise • Knowledge of regulatory submissions and serious adverse event reporting • Clinical trial data collection and medical monitoring experience • Excellent scientific communication and leadership skills • Ability to work effectively in cross-functional and global teams About the Company Emmes Group is a global clinical research organization with over 47 years of expertise supporting government and biopharma-sponsored studies. Emmes is a leader in cell and gene therapy, vaccines, rare diseases, neuroscience, and ophthalmology, dedicated to accelerating medical discovery and improving patient lives worldwide.