Medical Advisor – Structured Job Description
Role Title: Medical Advisor
Location: Mumbai, India
Category: Medical & Clinical Affairs
Job Type: Full-time
Role Summary
The Medical Advisor is a senior-level individual contributor role within Medical Affairs, responsible for overseeing the planning, execution, and management of complex clinical trials and research activities. The role requires strong scientific expertise and the ability to independently manage high-impact clinical and regulatory responsibilities, particularly in Phase III and Phase IV studies.
Key Responsibilities
1. Clinical Trial Leadership
Lead and oversee design, planning, and execution of clinical trials and research programs
Manage Phase III and Phase IV clinical studies for company products under development
Ensure proper implementation of clinical protocols and study methodologies
2. Investigator & Site Management
Recruit clinical investigators for study participation
Negotiate study design, budgets, and associated costs with investigators and stakeholders
Coordinate investigator meetings and group study activities
Oversee site initiation processes and ensure readiness
3. Regulatory & Compliance Activities
Ensure adherence to clinical trial protocols and regulatory requirements
Contribute to preparation and submission of clinical study reports to regulatory agencies
Support adverse event (AE) reporting and pharmacovigilance/safety monitoring activities
4. Data & Study Oversight
Monitor study progress and determine study completion criteria
Ensure data collection quality and consistency across trial sites
Facilitate completion of final clinical study reports
5. Cross-functional Collaboration
Act as liaison between internal teams and external partners
Collaborate with regulatory bodies, investigators, and potential licensing partners
Provide medical and scientific input across clinical development activities
Required Qualifications
Associate degree (minimum requirement noted)
Minimum 7 years of experience in Medical Affairs or clinical research-related roles
Strong experience in clinical trial management and oversight
Required Skills & Expertise
Deep knowledge of Medical Affairs processes and clinical development lifecycle
Strong understanding of Phase III and Phase IV clinical trials
Experience in adverse event reporting and safety monitoring
Ability to manage complex, multi-stakeholder clinical projects
Strong negotiation and communication skills
Familiarity with regulatory submission processes
Role Characteristics
Senior individual contributor with high autonomy
Works on complex and specialized clinical development projects
May deviate from standard approaches to develop effective solutions
Acts as a scientific and medical expert within the organization
Key Responsibilities Impact
Supports development and approval of pharmaceutical products
Ensures clinical evidence generation aligns with regulatory standards
Contributes directly to patient safety monitoring and study integrity
Influences clinical development strategy and execution
Work Context
This role operates within Medical & Clinical Affairs, supporting late-phase clinical development (Phase III–IV) and post-marketing research activities. It requires strong collaboration with investigators, regulatory authorities, and internal clinical development teams.
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
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Frank Scottile Blvd |Missouri :
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Germany | GErmany |Lower Saxony :
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Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
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Cork | Dublin | Limerick | Waterford |Ulster :
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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Arkansas | Remote Australia |New South Wales :
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Queensland |Melbourne :
South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
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Argentina | Peru |Brazil :
Sao paulo | Brazil |Attica :
Koropi | Athens |Greece :
Greece |North Island :
Auckland |New Zealand :
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Austria |Vienna :
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Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Estonia | Tartu |Harju County (Maakond) :
Tallinn |Hà Nội :
Hanoi | Hà Nội |Ho Chi Minh :
Ho Chi Minh City |Italy :
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Jakarta |East Java :
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Saitama | Japan |Tokyo :
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Oulu |Southwest Finland (Varsinais-Suomi) :
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King Abdullah Economic City | Najran | Khulais | Rabigh | Riyadh | Jeddah |Kuala Lumpur :
Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
Lima |France :
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Midrand | South Africa |Nišava District :
Niš |Bohemia :
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