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Key Responsibilities • Perform centralized medical review of clinical trial subject data • Ensure compliance with ICH-GCP, SOPs, protocol and regulatory requirements • Identify clinically significant data inconsistencies, trends and safety concerns • Collaborate with Data Managers, Trial Managers and Medical Specialists • Support trial planning activities related to medical review • Review Medical Monitoring Plans (MMP), data listings and monitoring displays • Present medical review findings for clinical decision-making • Resolve medical queries with investigational sites • Ensure medical review documentation is maintained in sponsor TMF • Escalate critical medical issues in accordance with blinding and communication plansRequired Qualifications • MBBS + MD • 2–5 years of experience in Clinical Research / Medical Review • Strong knowledge of ICH-GCP guidelines • Experience in risk-based monitoring methodologies • Familiarity with clinical trial data systems and tools • Strong MS Office / PowerPoint / MS Project skills • Excellent English communication and analytical skills • Ability to manage complex, independent responsibilitiesAbout the Department The Centralized Monitoring Unit (CMU), Bengaluru, supports Novo Nordisk’s global clinical drug development programs. Medical Reviewers collaborate with international medical specialists to ensure protocol compliance, detect clinically significant outliers, maintain data quality, and safeguard participant safety through advanced risk-based monitoring frameworks.Why Join Novo Nordisk • Work on global clinical development programs • Direct impact on patient safety and regulatory compliance • Collaborative international exposure • High career growth potential in Clinical Research & Medical Affairs

Key Responsibilities • Provide medical oversight for clinical trials across BA/BE and Phase studies • Review adverse events (AEs), serious adverse events (SAEs), and safety signals • Draft and review Integrated Summary of Safety and Efficacy (ISS/ISE) • Prepare and review Medical Monitoring Plans (MMP), Risk Management Plans, REMS and Safety Management Plans • Support preparation of Investigator’s Brochure, ICF, CSR and regulatory documents • Perform MedDRA and WHO Drug coding reviews • Generate and review SAE narratives and safety analyses • Conduct medical review of protocols and synopses • Lead site feasibility assessments and prepare SFQs • Train site and internal teams on protocol and safety procedures • Coordinate safety communication with stakeholders per ICH-GCP and SOP timelines • Travel to sites for monitoring activities as requiredCore Competencies • Patient safety oversight and risk-benefit evaluation • Regulatory and ethical compliance (ICH-GCP, local regulations) • Cross-functional collaboration with CRAs, statisticians and PV teams • Real-time data interpretation and safety trend analysis • High-impact communication and medical decision making • Protocol deviation detection and corrective action planningEducation & Experience • MBBS with MD (Pharmacology) – Mandatory • Foundational to early-career experience in clinical research or pharmacovigilance preferredRequired Skills • Clinical trial safety monitoring • SAE / AE medical review • Regulatory documentation • MedDRA / WHO-Drug coding • Data trend analysis • Investigator communication • Leadership and mentoringAbout Syngene Syngene International Ltd is an innovation-led Contract Research, Development and Manufacturing Organization (CRDMO) providing integrated scientific services from early discovery to commercial supply. Patient safety, data integrity, and ethical compliance form the core of Syngene’s research culture.

Role & Responsibilities • Provide outpatient and inpatient medical care to hospital patients • Diagnose and treat common medical conditions • Prescribe medications and treatment plans • Maintain accurate patient records and reports • Participate in emergency medical care and referrals • Follow hospital clinical and safety protocols Qualification • MBBS from a recognized medical institution • Valid medical council registration Experience • Freshers and experienced doctors eligible Skills • Clinical diagnosis and patient management • Prescription writing and documentation • Emergency handling skills • Communication and patient counselling • Ability to work in a hospital environment About the Company Ordnance Factory Hospital Chanda (OFCH) is a government healthcare facility operating under the Ordnance Factory Board, providing medical services to defence employees and their families while maintaining structured public health standards.

Role & Responsibilities Perform medical review of individual case safety reports (ICSRs) from clinical trials, literature, spontaneous sources and regulatory authorities Ensure correct assessment of adverse events for seriousness, expectedness and listedness Review MedDRA coding for adverse events, medical history and concomitant medications Validate causality assessment and product role classification (suspect, concomitant, interacting) Review case narratives for medical accuracy, clinical coherence and regulatory completeness Draft and medically review aggregate safety reports including PSURs and PADERs Review Risk Management Plans (RMPs) and signal management documentation Support pharmacovigilance medical writing and regulatory submission activities Qualification MBBS or MD (preferably Pharmacology) OR PharmD or M.Pharm with drug safety medical writing experience Experience 2–4 years of experience in pharmacovigilance medical review or drug safety medical writing Hands-on exposure to PSURs, PADERs, DSURs, RMPs and signal management reports Skills Strong knowledge of pharmacovigilance regulations and safety reporting standards Proficiency in ICSR medical review and aggregate report writing Accurate use of MedDRA terminology High attention to clinical detail and documentation quality Strong written and verbal communication skills Good organizational and time management skills Working knowledge of MS Office tools About the Company MSN Group is a vertically integrated pharmaceutical company with strong capabilities across APIs, formulations and drug delivery systems. The company operates structured pharmacovigilance and regulatory compliance frameworks supporting global markets, with a strong R&D-driven focus on documentation quality, lifecycle safety management and regulatory excellence.

Role & Responsibilities • Provide medical consultations and treatment to employees and dependents • Handle emergency and occupational health cases • Conduct routine medical examinations and health assessments • Maintain patient records and medical documentation • Ensure compliance with workplace health and safety protocols • Coordinate with hospital staff and occupational health teams Qualification • MBBS from a recognized medical institution Experience • Freshers and experienced doctors can apply Skills • Clinical diagnosis and patient management • Emergency handling and first aid response • Medical documentation and reporting • Good communication and patient care skills About the Company • Government-sector medical officer role providing comprehensive healthcare services at Oil India’s Occupational Health Centre in Duliajan, AssamStarting date31-12-2025Closing date20-01-2026Official Notification and Application FormClick Here

Role & Responsibilities • Perform consultative selling of high-value treatment plans, programs and memberships at clinic reception • Manage clinic front desk operations and handle customer escalations professionally • Ensure timely inventory backfill of medicines and maintain clinic facility standards • Comply with SOPs to achieve and maintain clinic operations excellence certification • Manage doctor schedules and appointment flow • Track sales KPIs, perform root cause analysis and implement improvement plans • Ensure brand hygiene, dress code, grooming and service quality standards • Support smooth day-to-day clinic operations including weekend working Qualification • Graduate in any discipline preferred Experience • Proven experience in consultative face-to-face selling at clinics, centres or retail healthcare setups • Prior experience managing clinic or centre operations is mandatory Skills • Strong sales and negotiation skills • Customer handling and escalation management • Operational planning and inventory coordination • KPI tracking and performance analysis • Leadership, ownership mindset and problem-solving ability About the Role This role leads front-end clinic operations and consultative selling of high-value healthcare services, ensuring sales growth, service excellence, SOP compliance and superior patient experience while independently managing clinic operations.

Role & Responsibilities • Perform patient history taking, vitals assessment and clinical documentation • Discuss patient findings with treating consultants for care plan formulation • Transcribe medical orders, prescriptions and investigation results into patient records • Maintain hard and soft copy documentation including reports, prescriptions, certificates and referrals • Prepare discharge summaries as directed by consultants • Transcribe ultrasound scan reports into electronic systems • Act as patient care coordinator for the centre • Explain procedures, pre-procedure instructions and visit flow to patients and couples • Educate patients about prescribed medications and treatment plans • Resolve patient queries and brief them on fertility treatment options • Liaise between patients, doctors and administrative teams to ensure smooth operations • Ensure compliance with healthcare regulations and patient safety standards Qualification • MBBS Experience • 2–4 years preferred in hospital / fertility clinic / clinical coordination role Skills • Clinical documentation and record management • Patient counselling and coordination • Good communication and interpersonal skills • Attention to detail and data accuracy • Ability to work in a multidisciplinary healthcare environment About the Role This role focuses on patient coordination, clinical documentation, counselling and liaison support within a fertility care centre to ensure high-quality patient experience, regulatory compliance and smooth day-to-day clinical operations.

Role & Responsibilities • Provide OPD consultation under senior specialists in Dermatology, Medicine and allied departments • Assist in clinical evaluation, diagnosis and patient management • Support departmental procedures and follow-up care • Participate in academic programs and case discussions • Work with modern diagnostic equipment including CT imaging • Maintain accurate patient records and documentation • Coordinate with nursing and support staff for smooth patient care Qualification • MBBS (Completed Internship) • FMGE qualified candidates eligible Experience • Freshers to early-career doctors • Suitable for NEET / USMLE aspirants seeking non-emergency OPD exposure Skills • Basic clinical examination and diagnostic skills • Medical documentation and record maintenance • Good communication and patient interaction • Willingness to learn and adapt • Team-oriented approach About the Role Hope Clinic is Meghalaya’s oldest private multi-specialty clinic established in 1992, offering doctors structured OPD exposure, advanced diagnostic facilities and regular academic programs in a stable day-shift working environment.

Role & Responsibilities • Work under the supervision of modern medicine doctors • Assist in patient assessment, daily progress notes and clinical documentation • Prepare discharge and death summaries • Support in maintaining medical records and hospital documentation • Coordinate with departments for patient evaluations and family meetings • Update doctors on patient condition and clinical changes • Assist in routine ward activities and patient care coordination • Be flexible to work in day, evening or night shifts as required • Support operations at other branches when assigned • Perform additional clinical and administrative responsibilities when requiredQualification • BAMS (Bachelor of Ayurvedic Medicine & Surgery)Experience • 1 – 3 years of clinical or hospital experienceSkills • Basic clinical assessment knowledge • Medical documentation and record keeping • Good communication and coordination skills • Ability to work under supervision • Flexible and cooperative work attitudeAbout the Role This role supports hospital doctors in daily clinical operations, documentation, patient coordination and inter-departmental communication while gaining exposure to hospital-based modern medical practice.

Role & Responsibilities • Provide in-person clinical consultations at primary health centres • Deliver teleconsultation via voice, video and chat • Diagnose and treat patients using standard clinical protocols • Prescribe treatment, counsel patients and refer when required • Maintain patient confidentiality and accurate medical records • Document medical histories, examination findings and reports • Participate in health camps at community and corporate levels • Ensure compliance with quality, safety and company policies • Stay updated with medical developments and treatment guidelinesQualification • MBBS degree • MCI / State Medical Council registration mandatoryExperience • Minimum 1+ year of clinical experienceSkills • Strong communication and listening skills • Empathetic and patient-centric approach • Multilingual – Hindi, English mandatory • Conversational Kannada required • Comfortable with split day shift • Good documentation and telemedicine handling skillsAbout the Company Clinikk is a health-tech company transforming primary healthcare for middle-income families in India. It combines affordable health insurance with protocol-based primary care to serve over 600 million uninsured Indians, backed by leading investors including Rajan Anandan, 500 Startups and Times Internet.

Role & Responsibilities • Conduct pre-employment and periodic medical examinations • Manage statutory medical check-ups for hazardous area employees • Conduct occupational health surveys and risk assessments • Ensure compliance with Factories Act and Gujarat Factories Rules • Liaise with certifying surgeons and health authorities • Develop and implement organizational medical policies • Operate and manage Occupational Health Centre (OHC) • Handle first-aid, emergency and accident response cases • Maintain ambulance readiness and emergency response systems • Manage medical stock, antidotes and emergency medicines • Coordinate with hospitals and specialists for referrals and camps • Conduct employee health awareness and hygiene programs • Train first aiders and conduct refresher programs • Manage biomedical waste disposal compliance • Prepare statutory reports, budgets and compliance documentation • Oversee procurement of medical and surgical suppliesQualification • MBBS degree from a recognized university • AFIH (Associate Fellow of Industrial Health) – MandatoryExperience • 2 to 5 years of occupational/industrial health experience • Experience in manufacturing or hazardous industry preferredSkills • Strong knowledge of occupational health laws and compliance • Emergency medical and industrial risk management • Training and employee engagement skills • Documentation and statutory reporting expertise • Proficiency in SAP, MS Excel, PowerPoint • Good communication in English and local languagesAbout the Company • Leading industrial organization focused on employee health and safety • Operates structured Occupational Health Centres across manufacturing units • Strong compliance-driven, employee-centric workplace culture

Role & Responsibilities • Provide OPD and IPD medical services (Medical Officer) • Handle maternal and child health programs (MCHO) • Maintain digital patient and program records (Data Entry Operator) • Assist public health initiatives and outreach programs • Prepare reports and maintain documentation • Follow NHM and government healthcare guidelinesName of the PostsVacanciesEducationMedical Officer02MBBS, MD/MSExperience • Freshers and experienced candidates can applySkills • Clinical diagnosis and patient care • Public health program coordination • Computer data entry and documentation • Government healthcare compliance • Communication and reporting skillsAge Limit • Minimum 21 years • Maximum 45 years • Relaxation as per government normsImportant Dates • Application Start – 31 December 2025 • Last Date – 09 January 2026Address for Submission Executive Secretary / District Health Officer District Health Society Old Nattamai Building Salem – 636001Official Notification and Application FormClick Here

Role & Responsibilities • Provide OPD and IPD medical services • Diagnose, treat and manage patients • Handle emergency medical care • Maintain medical records and reports • Follow government healthcare protocolsQualification • MBBS from a recognized medical institution • Must be registered with State Medical CouncilVacancies 117 PostsExperience • Freshers and experienced doctors can applySkills • Clinical diagnosis and patient care • Emergency handling • Medical documentation • Government healthcare complianceAge Limit • Minimum 21 years • Maximum 45 years • Age relaxation as per government normsSelection Process • Tamil Language Eligibility Test • Computer Based TestSalary • ₹50,000 – ₹1,00,000 per monthApplication Fee • SC / SCA / ST / DAP – ₹500 • All Others – ₹1000Important Dates • Application Start – 24 December 2025 • Last Date – 13 January 2026Official NotificationClick Here

Role & Responsibilities Perform end-to-end ICSR case processing Triage, prioritize and assess adverse event cases Conduct MedDRA and WHO-Drug coding Assess seriousness, causality and expectedness Draft narratives and sender comments Manage follow-ups, reconciliations and regulatory timelines Support inspections, audits and safety surveillance activities Handle literature review and mailbox management Qualification Bachelor of Ayurvedic Medicine and Surgery (BAMS) Bachelor’s Degree in Life Sciences Master’s Degree in Life Sciences Experience 1–3 years of pharmacovigilance experience Skills Strong knowledge of pharmacovigilance workflows Good command over MedDRA and WHO-Drug coding Medical writing and documentation skills Proficiency in MS Office tools Excellent communication and compliance orientationAbout the Company Accenture is a global professional services organization with large-scale life sciences operations Works with international clients and regulatory frameworks Offers long-term growth in drug safety and pharmacovigilance careers

Role & Responsibilities Update and maintain patient files during follow-up visits Record and maintain complete medical histories and patient information Perform daily OPD under the supervision of a senior doctor Assist senior doctors in primary consultation and clinical assessment Support prescribing of medications and provide OPD and IPD care Conduct clinical examination of couples and analyze investigation reports and test results Maintain accurate and clear medical documentation Assist doctors during sonography procedures Explain prescriptions and treatment plans to patients as per consultant’s advice Maintain IPD records, admission notes and discharge summaries Guide nursing staff for IPD patient care as per doctor’s guidelines Monitor medication administration and ward activities Qualification BAMS or BHMS Experience Minimum 2 years of relevant clinical experience Skills Clinical examination and patient assessment Medical documentation and record management Patient counseling and communication Basic sonography assistance Coordination with nursing staffAbout the Company Progenesis is a leading fertility healthcare organization dedicated to helping couples overcome infertility and achieve parenthood. Established in 2014, Progenesis provides compassionate, ethical and evidence-based fertility care and supports couples through every stage of their reproductive journey.

Role & Responsibilities Provide preventive, promotive, curative and emergency medical services to employees and their families Manage and operate Medical Centres independently Deliver routine and emergency treatment through in-person and virtual modes Implement emergency and disaster management protocols Coordinate with hospitals, ambulance services and EMS providers Implement uniform emergency management protocols across assigned zones Support development of medical infrastructure and wellness initiatives Conduct pre-employment and periodic health check-ups Plan and deliver first aid and occupational health trainings Implement ergonomic and indoor air quality (IAQ) health services Support corporate and sports events as required Prepare daily, weekly and monthly medical reports Conduct internal audits Engage with state leadership teams and business leaders Handle medical concerns of senior leadership Qualification MBBS (Mandatory) Postgraduate Diploma / AFIH / Emergency Training preferred Experience Minimum 5+ years of medical practice Experience in corporate offices, hospitals or offshore installations preferred Prior experience in multi-location liaison and coordination preferred Skills Clinical diagnosis and patient assessment Emergency care and disaster response Healthcare compliance and documentation Occupational health services

Role & Responsibilities Conduct post-discharge follow-up teleconsultations Monitor recovery progress and identify early warning signs Assess medication, laboratory, diet and physiotherapy adherence Provide evidence-based clinical guidance (non-prescribing) Escalate high-risk cases to the clinical team Educate patients on lifestyle modifications and self-care practices Coordinate referrals, diagnostic services and allied healthcare support Maintain accurate electronic medical records Collaborate with program managers to improve care delivery models Qualification MBBS (Mandatory) Additional certification in Family Medicine or Public Health is an advantage Experience 2–4 years of clinical practice preferred Family Medicine, Internal Medicine, Emergency or Community Health experience desirable Skills Strong clinical judgment and analytical ability Excellent communication and patient counselling skills Knowledge of post-hospitalization recovery protocols Ability to prevent readmissions through early intervention Familiarity with teleconsultation platforms preferred Benefits Fixed daytime working hours Permanent employment Exposure to digital healthcare and population health programs Career growth in HealthTech and Value-Based Care systemsAbout the Company HEAPS Health Solutions is a health-tech organization headquartered in Bangalore with offices in Mumbai, Hyderabad and Delhi. The company leverages data analytics, artificial intelligence and machine learning to deliver value-based digital healthcare and patient care coordination services.

Role & Responsibilities Maintain global oversight of unresolved sample discrepancies for incoming and outgoing shipments Coordinate with internal teams to resolve discrepancies within defined TAT and OTIF timelines Perform QC verification of biospecimen data in LIMS and inventory systems Conduct advanced QC checks and trend analysis on sample data Support study close-out activities including reconciliation of sample disposition Monitor patient sample collection schedules and protocol assessment windows Support study setup activities in LIMS including workflows and protocol configuration Prepare operational reports including inventory, kit tracking and site performance metrics Participate in RCA and CAPA activities Ensure compliance with QMS, SOPs and data privacy regulations Support ad-hoc analysis and cross-functional operational requests Qualification Bachelor’s or Master’s degree in Life Sciences or related discipline Experience Minimum 2–3 years of experience in clinical research, sample management or data operations Skills Strong understanding of drug, device and biologic development processes Hands-on experience with clinical databases and LIMS systems Expertise in data quality and compliance standards Proficiency in MS Excel, Word, PowerPoint and Outlook Excellent written and verbal communication skills Knowledge of GDPR, HIPAA and data privacy regulations About the Company Precision For Medicine is a global precision medicine organization supporting international clinical trials, biospecimen management and advanced clinical data operations

Role & Responsibilities Perform triage and initial validity assessment of adverse event cases Enter and manage safety data in global pharmacovigilance databases Conduct initial ICSR assessments as per regulatory requirements Evaluate cases for expedited reporting and regulatory timelines Prepare and submit CIOMS I, MedWatch and XML safety reports Draft follow-up queries to collect missing case information Maintain audit-ready documentation Retrieve and assess cases from EVWEB and health authority sources Support additional pharmacovigilance activities as assigned Qualification B.Pharm / M.Pharm BDS Life Science Graduate Experience Freshers / Entry-level candidates preferred Skills Strong written and verbal communication Attention to detail and compliance mindset Basic understanding of pharmacovigilance and drug safety Willingness to learn global PV regulations Time management and documentation skills About the Company Cencora, through PharmaLex India, is a global healthcare services organisation delivering regulatory, pharmacovigilance and risk management solutions while ensuring patient safety and compliance across international markets