Job Description
Designation: VP / Sr. VP - Global Medical Affairs
Location: Ahmedabad
Job Summary
A leading CRO is seeking a senior medical and scientific leader to head its Global Medical Affairs function. The role will be responsible for defining and executing the global medical and scientific strategy, ensuring regulatory compliance, scientific excellence, and operational effectiveness across regions. This position will oversee Medical Affairs, Pharmacovigilance, Clinical Data Management, Biostatistics, Programming, and Medical Writing, while supporting product lifecycle management and evidence generation globally.
The role also carries accountability for driving business growth through strategic initiatives and effective leadership of the Medical & Scientific Affairs portfolio.
Key Responsibilities
Define and execute the global medical and scientific affairs strategy aligned with organisational objectives.
Provide executive oversight across clinical programs, ensuring scientific integrity, regulatory compliance, and operational efficiency.
Drive strategic initiatives that contribute to revenue growth and long-term financial sustainability.
Oversee global pharmacovigilance systems, risk management plans, and medical governance frameworks.
Lead and manage all functions within Medical & Scientific Affairs, including PV, CDM, Biostatistics, Programming, and Medical Writing.
Partner closely with R&D, Regulatory, Commercial, and Clinical teams to support product development and lifecycle management.
Drive real-world evidence generation, clinical trial support, publications, and data-driven insights.
Build, mentor, and lead a high-performing global medical team, including regional and functional heads.
Qualifications
MD / Ph D in Life Sciences or a related discipline; advanced degree preferred.
15+ years of experience in Medical Affairs, Clinical Research, or related functions within pharma, biotech, or CRO environments.
Proven experience leading global, cross-functional, and cross-cultural teams.
Strong understanding of global regulatory requirements including FDA, EMA, and ICH guidelines.
Demonstrated ability to combine scientific leadership with strategic and financial acumen.
Strong communication, stakeholder management, and decision-making capabilities.
Location: Ahmedabad
Job Summary
A leading CRO is seeking a senior medical and scientific leader to head its Global Medical Affairs function. The role will be responsible for defining and executing the global medical and scientific strategy, ensuring regulatory compliance, scientific excellence, and operational effectiveness across regions. This position will oversee Medical Affairs, Pharmacovigilance, Clinical Data Management, Biostatistics, Programming, and Medical Writing, while supporting product lifecycle management and evidence generation globally.
The role also carries accountability for driving business growth through strategic initiatives and effective leadership of the Medical & Scientific Affairs portfolio.
Key Responsibilities
Define and execute the global medical and scientific affairs strategy aligned with organisational objectives.
Provide executive oversight across clinical programs, ensuring scientific integrity, regulatory compliance, and operational efficiency.
Drive strategic initiatives that contribute to revenue growth and long-term financial sustainability.
Oversee global pharmacovigilance systems, risk management plans, and medical governance frameworks.
Lead and manage all functions within Medical & Scientific Affairs, including PV, CDM, Biostatistics, Programming, and Medical Writing.
Partner closely with R&D, Regulatory, Commercial, and Clinical teams to support product development and lifecycle management.
Drive real-world evidence generation, clinical trial support, publications, and data-driven insights.
Build, mentor, and lead a high-performing global medical team, including regional and functional heads.
Qualifications
MD / Ph D in Life Sciences or a related discipline; advanced degree preferred.
15+ years of experience in Medical Affairs, Clinical Research, or related functions within pharma, biotech, or CRO environments.
Proven experience leading global, cross-functional, and cross-cultural teams.
Strong understanding of global regulatory requirements including FDA, EMA, and ICH guidelines.
Demonstrated ability to combine scientific leadership with strategic and financial acumen.
Strong communication, stakeholder management, and decision-making capabilities.
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