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About Role & Responsibilities • Review, assess and medically evaluate adverse event reports • Ensure accurate medical coding and causality assessment • Provide medical oversight for ICSR processing and signal detection • Support aggregate safety reporting and regulatory submissions • Participate in safety governance and risk management activities • Liaise with regulatory authorities and global stakeholders Qualification MBBS / MD Experience Minimum 5+ years in pharmacovigilance or clinical safety Skills • ICSR processing • Medical review & causality assessment • Aggregate safety reports (PSUR, PBRER, RMP) • Regulatory compliance • Excellent documentation and communication skills About the Company Indegene is a global healthcare solutions company providing technology-driven services across medical, regulatory and safety domains to leading pharmaceutical and life-science companies worldwide
About the role & responsibilities • Provide inpatient and outpatient clinical services • Assist consultants in diagnosis, treatment and patient management • Participate in ward rounds and emergency care services • Maintain medical records and documentation • Support academic, clinical and research activitiesName of the PostsNo.of VacanciesQualificationSenior Resident 04MBBS, MD/ MS Experience • Freshers and experienced candidates eligible Skills • Clinical diagnosis and treatment • Emergency and inpatient care • Medical documentation • Communication and teamwork About the company • Indira Gandhi Institute of Medical Sciences (IGIMS) is a leading government medical institute How to apply • Attend walk-in interview on 19-01-2026Application formClick HereOfficial NotificationClick Here
Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
About the role & responsibilities • Provide specialized medical services under National Health Mission programs • Diagnose and treat patients in assigned healthcare facilities • Support public health initiatives and outreach programs • Maintain medical records and reporting documentation Name of the PostsNo.of VacanciesQualificationSpecial Doctor 300MBBS, MD/ MS, DNB, Post Graduation Experience • Freshers and experienced candidates eligible Skills • Specialized clinical care • Patient communication • Medical documentation • Public health program knowledge About the company • National Health Mission Punjab delivers public healthcare services across the stateOfficial NotificationClick Here
About the role & responsibilities • Provide medical care to patients under District Health Society programs • Conduct clinical examinations and diagnosis • Prescribe treatment and monitor patient progress • Support public health initiatives and reporting requirements Qualification • MBBS Experience • Freshers and experienced candidates eligible Skills • Clinical diagnosis and treatment • Patient care and communication • Knowledge of public health programs • Medical documentation skills About the company • District Health Society Kancheepuram operates public healthcare programs in Tamil Nadu How to apply • Send filled application to: Administrative Secretary, District Health Officer, District Health Society, 42A, Railway Road, Arignar Anna Memorial Cancer Complex, Kancheepuram – 631501Official Notification and Application FormClick Here
About the role & responsibilities • Provide routine inpatient medical care • Manage after-hours admissions and patient assessments • Support specialists and nursing teams in clinical care delivery • Assess newly admitted and deteriorating patients • Ensure compliance with NSQHS and infection control standards Qualification • MBBS or equivalent • Full unrestricted AHPRA registration Experience • PGY3+ • Minimum 3 years post-graduate acute care experience Skills • Acute patient management • Advanced Life Support • Strong communication and teamwork • Knowledge of NSQHS and WHS standards About the company • St Stephens Hospital is Australia’s first fully digital not-for-profit private hospital
About the role & responsibilities • Deliver comprehensive general practice care with focus on chronic disease management • Provide preventative health services and GP care plans • Build long-term relationships with patients • Maintain continuity of care and high-quality clinical standards Qualification • FRACGP / FACRRM • Current AHPRA registration Experience • Experienced VR General Practitioner Skills • Chronic disease management • Preventative health care • Strong patient communication • Clinical autonomy and decision making About the company • Flinders Clinic is a modern family medical practice focused on sustainable, patient-centred care
About the role & responsibilities • Perform triage and validity assessment of adverse event reports • Enter and process ICSRs in global safety databases • Assess cases for expedited reporting timelines • Prepare CIOMS, MedWatch and XML safety reports • Draft follow-up queries to obtain missing case information • Retrieve and review EVWEB cases • Maintain audit-ready safety documentation • Support additional pharmacovigilance activities Qualification • B.Pharm / M.Pharm • BDS • Life Science graduate Experience • Freshers and early-career candidates eligible Skills • Pharmacovigilance and ICSR processing knowledge • Strong communication skills • High attention to detail • Ability to meet regulatory timelines About the company • Cencora (PharmaLex India Private Limited) is a global healthcare services organization focused on drug safety and regulatory compliance
About the role & responsibilities • Act as CTMS subject matter expert and support system upgrades and user queries • Develop and maintain CTMS training materials and training matrix • Manage global trial disclosures and ensure regulatory compliance • Maintain eTMF systems as per DIA reference model and SOPs • Support LMS coordination and training documentation • Contribute to SOP review and quality compliance activities • Create dashboards and analytics using Power BI and BI tools • Perform data integrity and validation checks • Coordinate with internal and external stakeholders Qualification • Master’s in Science / Computers / Advanced Data Analytics • Equivalent industry experience accepted Experience • Minimum 5 years in pharma, IT software or data analytics domain Skills • CTMS, eTMF and Trial Disclosure management • Dashboard and BI analytics • SOP and compliance knowledge • MS Excel and MS Word proficiency • Strong documentation and multitasking skills About the company • Abbott Leading global pharmaceutical organization
About the role & responsibilities • Provide on-site clinical education and product training to healthcare professionals • Support surgeons during procedures and provide case coverage • Act as technical expert for assigned surgical and medical device products • Assist sales teams in territory planning and execution • Support clinical workshops, CMEs and conferences • Identify growth opportunities with regional sales and clinical teams • Coordinate closely with clinical leads and sales managers Qualification • B.Sc / B.Pharm / B.Tech Biomedical / Life Sciences Experience • 0 years • Freshers eligible Skills • Clinical and surgical technology interest • Strong communication and interpersonal skills • Willingness to travel for case support • Ability to work with sales and clinical teams About the company • Medtronic is a global leader in healthcare technology focused on life-saving innovations
About the role & responsibilities • Review and contribute to Safety Data Exchange Agreements ensuring quality and compliance • Support preparation of licensing agreements within assigned therapeutic areas • Participate in internal project-focused medical safety meetings • Engage in external scientific and non-regulatory meetings with consultants and partners • Maintain audit and inspection readiness • Lead or support safety process improvement initiatives • Provide medical safety support for US and RoW case management functions • Review and approve investigator safety reports with Clinical Development physicians Qualification • MBBS / MD Experience • Minimum 3 years in signal management, safety report authoring and benefit–risk management planning Skills • Signal management • Safety report writing and review • Benefit–risk evaluation • Regulatory compliance understanding • Strong analytical and communication skills About the company • Tata Consultancy Services (TCS) is a global IT and digital transformation leader with strong life sciences and healthcare operations
About the role & responsibilities • Develop global value dossiers, value briefs, scientific abstracts, manuscripts, and presentation decks • Create infographics, summaries, and HEOR scientific communication tools • Ensure clarity, consistency, and visual impact of all HEOR materials • Collaborate with Medical Affairs, Market Access and R&D teams on scientific narratives • Coordinate and track global HEOR projects, timelines and deliverables • Maintain dashboards, reports, and leadership updates • Support internal meetings, documentation and project follow-ups • Contribute to differentiated HEOR work products and scientific publications • Perform basic cost calculations and budget impact support (preferred) Qualification • Master’s degree or higher in Health Economics, Public Health, or related field Experience • Minimum 5+ years in HEOR, medical writing, or scientific communications Skills • HEOR scientific writing and editing • PowerPoint and Word proficiency • Strong analytical and project coordination skills • Excellent English communication skills • Ability to manage multiple priorities and collaborate cross-functionally About the company • Alcon is the global leader in eye care, dedicated to improving sight and patient lives through innovation
About the role & responsibilities • Build and maintain strong scientific relationships with healthcare professionals and KOLs • Engage in non-promotional scientific discussions on products and therapy areas • Deliver scientific presentations, CMEs, advisory boards and TOT programs • Generate medical insights from HCP interactions and surveys • Support clinical trial and investigator engagement activities • Align medical affairs strategies with India business priorities • Educate and train internal stakeholders on product science and medical practices • Collaborate with professional associations for guideline development and dissemination • Advise business leaders on medical and scientific matters • Represent company at scientific meetings and medical forums Qualification • MBBS / BDS / Postgraduate in relevant discipline Experience • Minimum 1+ year of medical affairs / scientific liaison experience Skills • Strong interpersonal, analytical and communication skills • Scientific presentation and stakeholder engagement • Proficiency in Excel and PowerPoint • Ability to multitask in fast-paced environments About the company • Haleon is a global consumer healthcare company with leading brands including Sensodyne, Panadol, Voltaren and Centrum, delivering trusted everyday health solutions worldwide
About the role & responsibilities • Act as scientific ambassador for oncology portfolio • Engage with KOLs and healthcare professionals for peer-to-peer scientific exchange • Deliver balanced, evidence-based medical information • Conduct advisory boards, CMEs, and scientific roundtables • Implement country-level medical affairs plans aligned to global strategy • Generate actionable medical insights for lifecycle management • Support real-world evidence generation • Drive scientific support for oncology product launches • Train internal commercial and marketing teams on disease and product science • Collaborate with clinical development, regulatory, market access and commercial teams • Ensure compliance with ICH-GCP, SOPs and regulatory guidelines • Perform adverse event and product complaint reporting Qualification • MBBS / MD / PhD / equivalent advanced degree in life sciences Experience • Minimum 2+ years in medical affairs or MSL role in oncology Skills • Strong oncology and biomarker knowledge • Excellent scientific communication and presentation skills • KOL relationship building and stakeholder engagement • Clinical trial data interpretation • Strategic planning and analytical thinking • Proficiency in MS Office and CRM tools Location & territory • North India region About the company • A global research-driven biopharmaceutical organization focused on developing innovative medicines and vaccines that improve patient outcomes
About the role & responsibilities • Execute Medical Affairs Plans for pre-launch and newly launched products • Engage in scientific exchange with healthcare professionals, key opinion leaders and ecosystem stakeholders • Provide scientific, clinical and pharmaco-economic information to HCPs • Develop and maintain peer-level scientific relationships • Conduct advisory boards, symposiums, MSL events, scientific exchanges and educational programs • Support evidence generation, investigator-initiated studies and publications • Gather medical insights on disease trends, patient pathways and treatment gaps • Support pharmacovigilance activities and adverse event reporting • Maintain compliance with ethical standards, GCP and regulatory guidelines • Deliver scientific training and presentations to internal and external stakeholders Qualification • Master’s degree in a scientific discipline • Doctoral degree preferred (MD / PhD / PharmD) Experience • Experience in pharmaceutical industry, medical affairs or clinical research preferred • Exposure to therapeutic area and KOL engagement Skills • Strong scientific communication and presentation skills • Stakeholder engagement and relationship management • Project management and analytical thinking • Knowledge of pharmacovigilance and GxP standards • Digital and technology-enabled scientific engagement About the company • AstraZeneca is a global science-led biopharmaceutical company focused on developing innovative medicines for serious diseases worldwide
About the role & responsibilities • Perform medical review of adverse events for investigational and marketed products • Ensure accurate medical assessment using MedDRA, WHO-DRL and ARGUS safety database • Maintain compliance with global pharmacovigilance regulations and internal SOPs • Identify, communicate and manage potential safety risks and safety signals • Provide medical review for aggregate safety reports including PSURs, PADERs and annual reports • Collaborate with safety and pharmacovigilance teams for consistent case assessment • Interact with sponsor safety and medical teams when required • Support training and mentoring of pharmacovigilance associates • Maintain continued medical education and PV expertise Qualification • MD / MBBS / DO • Completed accredited residency Experience • 1–2 years of clinical practice • Minimum 1 year experience in Pharmacovigilance / Drug Safety in pharma, CRO or biotech Skills • Knowledge of global PV regulations • MedDRA and WHO-DRL coding understanding • ARGUS safety database exposure • Safety signal identification and risk assessment • Strong documentation and communication skills About the company • Syneos Health is a global biopharmaceutical solutions organization operating in 110+ countries, supporting clinical development, medical affairs and commercialization worldwide Location & travel • Location as per project | Travel up to 10%
About the role & responsibilities • Perform medical review of adverse event cases for investigational and marketed products • Ensure accurate medical assessment using MedDRA, WHO-DRL and safety databases (ARGUS) • Maintain regulatory and SOP compliance for safety reporting and surveillance • Identify, communicate and manage safety signals and potential safety risks • Review aggregate safety reports including PSURs, PADERs and annual safety reports • Provide scientific and medical input to pharmacovigilance teams • Interact with sponsor safety and medical teams • Support training, mentoring and development of PV associates • Maintain continuous medical education and PV expertise Qualification • MD / MBBS / DO with completed residency Experience • 1–2 years clinical practice experience • 1+ year experience in Pharmacovigilance / Drug Safety in pharma, CRO or biotech Skills • Strong knowledge of global PV regulations • MedDRA & WHO-DRL coding understanding • ARGUS safety database experience • Signal detection & case medical review • Scientific writing & communication • Regulatory compliance & documentation About the company • Syneos Health is a global biopharmaceutical solutions organization operating across 110+ countries, supporting drug development, medical affairs and commercialization programs worldwide
Join a leading tertiary care hospital. Responsibilities include medication therapy management. **Job Duties:** - Diagnose and treat patients. - Prescribe medications as necessary. - Order and interpret diagnostic tests. - Advise patients on preventative health. **Benefits:** - Health insurance. - Paid time off. - Continuing education support.
World-class hospital seeking Board Certified Consultant Cardiologists. **What you will do:** - Lead daily clinical operations. - Mentor junior staff members. - Participate in quality improvement initiatives. **Requirements:** - Proven experience in the field. - Strong communication skills. - Valid license and registration.
About Role & Responsibilities • Serve as a scientific resource for healthcare professionals, providing expert knowledge on medical products and disease areas • Facilitate peer-to-peer scientific discussions with key opinion leaders (KOLs) • Support clinical research and assist in the development of medical strategies • Provide training and scientific support to internal teams and external stakeholders • Maintain a deep understanding of scientific advancements and regulatory requirements Qualification • PhD, PharmD, or MD Experience • 2+ years of experience in medical affairs or a related field Skills • Strong scientific knowledge and communication skills • Ability to engage with KOLs and healthcare professionals • Understanding of clinical data and regulatory requirements About the Company Novartis India is a leading global healthcare company focused on providing life-saving treatments and improving health worldwide