Medical Advisor
Company: Abbott
Location: Mumbai, India
Department: Medical & Clinical Affairs
Employment Type: Full-Time
Experience Required: 7+ Years
Function: Medical Affairs / Clinical Research / Medical Strategy
Position Overview
Abbott is seeking an experienced Medical Advisor to provide scientific, clinical, and strategic leadership within the Medical Affairs function. This role is responsible for supporting clinical development programs, overseeing Phase III and Phase IV clinical studies, ensuring patient safety, generating scientific evidence, and collaborating with cross-functional teams to support product lifecycle management.
The Medical Advisor serves as a key medical expert, providing clinical insights, scientific guidance, and regulatory support while maintaining strong relationships with investigators, healthcare professionals, and external stakeholders.
Key Responsibilities
Medical Affairs Leadership
Serve as a subject matter expert within the Medical Affairs organization.
Provide strategic medical and scientific input for assigned therapeutic areas and products.
Support the development and execution of medical affairs plans aligned with business objectives.
Deliver evidence-based medical insights to internal and external stakeholders.
Clinical Research & Trial Management
Oversee and support Phase III and Phase IV clinical studies.
Contribute to protocol development, study design, and scientific review processes.
Ensure successful execution of clinical research projects according to timelines and quality standards.
Monitor study progress and ensure compliance with approved protocols.
Facilitate study completion and review final clinical study reports.
Investigator & Site Management
Identify, recruit, and engage clinical investigators and research centers.
Build and maintain strong relationships with healthcare professionals and key opinion leaders (KOLs).
Coordinate investigator meetings, site initiations, and study-related activities.
Negotiate study requirements, budgets, and operational deliverables.
Medical Monitoring & Patient Safety
Participate in medical monitoring activities throughout the clinical trial lifecycle.
Review and assess adverse events, serious adverse events, and safety signals.
Support pharmacovigilance activities and safety surveillance programs.
Ensure patient safety remains the highest priority across all studies.
Regulatory Affairs Support
Collaborate with Regulatory Affairs teams on clinical and scientific submissions.
Support preparation and review of documents submitted to regulatory authorities.
Provide medical expertise for regulatory queries and health authority interactions.
Ensure compliance with global and local regulatory requirements.
Scientific Communications
Interpret clinical trial data and scientific evidence.
Develop scientific presentations, reports, publications, and educational materials.
Communicate complex medical information clearly to healthcare professionals and internal teams.
Support medical education initiatives and scientific exchange activities.
Cross-Functional Collaboration
Work closely with:
Clinical Operations
Regulatory Affairs
Pharmacovigilance
Medical Information
Commercial Teams
Market Access
Research & Development
Quality Assurance
to ensure alignment of clinical, scientific, and business objectives.
Compliance & Quality
Ensure all activities comply with:
ICH-GCP Guidelines
Local Regulatory Requirements
Company Policies
Ethical Standards
Industry Best Practices
Maintain inspection readiness and support audits when required.
Promote a culture of quality, compliance, and patient safety.
Required Qualifications
Education
Preferred
MBBS
MD (Preferred)
PharmD
Alternative Qualifications
Master's Degree in Life Sciences
Clinical Research
Pharmacology
Biotechnology
Related Healthcare Discipline
Experience Requirements
Mandatory
Minimum 7 years of experience in:
Medical Affairs
Clinical Research
Clinical Development
Pharmaceutical Industry
Biotechnology Industry
Preferred
Experience in:
Clinical Trial Management
Medical Monitoring
Pharmacovigilance
Regulatory Affairs
Investigator Management
Scientific Communications
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