Medical Physician Specialist II – Mumbai
Full-Time | Job ID: 255708
Application Deadline: November 24, 2025
Job Overview
The Medical Physician Specialist II will provide advanced medical safety expertise in the post-marketing phase for pharmaceutical products, medical devices, and combination products. This role focuses on medical case evaluation, clinical safety decision-making, and ensuring regulatory-compliant pharmacovigilance practices.
Key Responsibilities
Medical Case Review
Conduct primary medical review of individual case safety reports, including seriousness assessment, labeling/listedness evaluation, causality assessment, adverse event coding, and narrative verification.
Complete daily documentation of case data and feedback using standardized trackers and workflow tools.
Quality, Compliance, and Delivery
Take full responsibility for all assigned safety deliverables in alignment with quality standards, regulatory compliance, productivity targets, and client SLAs/KPIs.
After one year of tenure, provide medical training and guidance to case processing teams.
Quality Control & Assurance
Perform secondary medical review (QC) and retrospective medical case evaluations (QA) after more than one year of service to identify error trends, training needs, and opportunities for process improvement.
Safety Surveillance
Support aggregate medical review processes and participate in signal detection and safety trend analysis as required.
Client Engagement & Process Improvement
Contribute to strengthening client relationships through consistent delivery and professional communication.
Promote a high-service culture and actively participate in internal process optimization initiatives.
Minimum Qualifications
Bachelor’s degree in Medical Science, or an MD/DO or equivalent medical qualification.
Relevant and equivalent experience may be considered in place of formal educational requirements.
Proficiency in English:
Speaking: ILR 3+
Reading/Writing: ILR 4+
Experience Required
Foundational understanding of medical sciences, diagnosis, therapeutics, and clinical procedures.
Knowledge of regulatory guidelines for clinical research and familiarity with ICH-GCP.
Preferred Experience
Up to 1 year of pharmaceutical industry experience, including pharmacovigilance (case processing or medical review) or clinical research.
1 to 2 years of clinical practice experience.
Understanding of pharmacovigilance regulations and safety reporting requirements.
Work Environment
May be office-based or home-based depending on business needs and manager approval.
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | Tarasadi | Vadodara | Vapi |Maharashtra :
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Bangalore | Belgaum | Bengaluru | B.G Nagara | Bommasandra | Colorado | Czech Republic | Karnataka | Mangaluru | Mysore | Udupi |Punjab :
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Delhi | India | New Delhi | PAN-India |Assam :
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Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Frank Scottile Blvd |Missouri :
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Germany | GErmany |Lower Saxony :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Norway | NOrway |Romania :
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Donegal |Meath :
Dunboyne |Dún Laoghaire :
Dún Laoghaire |Galway :
Galway |County Dublin :
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Beijing |China :
China | Quarry Bay |Liaoning :
Dalian |Zhejiang :
Hangzhou |Tokiyo :
Osaka | Tokyo |Shanghai Sai :
Shanghai Shi |Hubei :
Wuhan |Capital of Netherland :
Amsterdam |North Brabant :
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Leiden |Netherlands :
Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
Ballina | Sydney |Republic of Western Australia :
Nedlands |Queensland :
Queensland |Melbourne :
South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
Harrogate |South Yorkshire :
Sheffield |Oxfordshire :
Witney |Ontario :
Mississauga | Uxbridge | Richmond Hill | Australia | North York | Renfrew |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
Zaventem |South America :
Peru | Argentina |Brazil :
Brazil | Sao paulo |Attica :
Koropi | Athens |Greece :
Greece |North Island :
Auckland |New Zealand :
New Zealand |Austria :
Austria |Vienna :
Vienna |Catalonia :
Barcelona |Madrid :
Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
Hanoi | Hà Nội |Ho Chi Minh :
Ho Chi Minh City |Italy :
Italy |Lombardy :
Rho |Jakarta :
Jakarta |East Java :
Surabaya |Japan :
Saitama | Japan |Tokyo :
Otemachi |North Ostrobothnia :
Oulu |Southwest Finland (Varsinais-Suomi) :
Turku |Remote Korea :
Remote Korea |Republic of Korea :
Seoul |Kazakhstan :
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Bangkok |Israel :
Netanya | Kfar Saba | Yavne | Tel Aviv | Be'Er Sheva |Remote :
McFarland | Green Way | Springville | Nairobi | Remote - South America (Latin Americal) | French | Melbourne | Remote, USA | Zaragoza | Medan | Lenexa | Switzerland | Remote - Africa | Bountiful | Remote | Castlebar | Leinster | Bishop | Lousiana | Thailand | Regulatory Labeling Manager (NA and LATAM Only) | Hungary | Texas | Riga | Faridabad | Remote - Europe | Belgium | Tulsa | Minnesota | Ireland | Remote - Middle East | Hammond | Manipal | Slovakia | Victoria | Blue Bell | Xzagreb |Republic of Colombia :
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Brentwood |Bucharest :
Bucharest |Buenos Aires :
Buenos Aires |Republic of Egypt :
Cairo |Mexico :
Ciudad de México | New Mexico |Dubai :
Dubai |Makkah :
Rabigh | Jeddah | King Abdullah Economic City | Khulais | Najran | Riyadh |Kuala Lumpur :
Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
Lima |France :
Paris | Lyon |South Africa :
Midrand | South Africa |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
Sarajevo |Singapore :
Singapore |Sofia City :
Sofia |Sweden :
Sweden |Taipei :
Taipei |Mazovia :
Warsaw |