Regional Medical Advisor
Location: Ahmedabad, Gujarat, India
Function: Medical and Clinical Affairs
Employment Type: Full-Time
Company Overview
Abbott Laboratories is a global healthcare leader focused on delivering innovative medicines, diagnostics, nutrition, and medical devices. With a strong footprint in India, Abbott continues to advance clinical excellence and evidence-based medical engagement across therapeutic areas.
Role Overview
The Regional Medical Advisor is a field-based medical affairs professional responsible for overseeing clinical research activities, supporting investigator-led studies, and ensuring compliance with regulatory and pharmacovigilance requirements within the assigned region.
This role plays a critical part in strengthening scientific engagement, supporting Phase III and IV clinical trials, and maintaining high standards of clinical governance. It is an ideal opportunity for medical affairs professionals seeking regional medical advisor jobs in Ahmedabad within a global pharmaceutical organization.
Key Responsibilities
Clinical Research & Trial Oversight
Provide medical leadership in the planning, execution, and monitoring of Phase III and Phase IV clinical trials.
Support implementation of clinical protocols and facilitate timely completion of final study reports.
Recruit and engage clinical investigators, including negotiation of study design and budgets.
Monitor adherence to study protocols and ensure timely study completion.
Medical Affairs & Scientific Engagement
Act as a regional scientific resource for internal and external stakeholders.
Coordinate investigator meetings, site initiations, and collaborative group studies.
Serve as a liaison in licensing partnerships or collaborative agreements where required.
Regulatory & Safety Compliance
Participate in adverse event (AE) reporting and pharmacovigilance monitoring.
Ensure compliance with regulatory guidelines, Good Clinical Practice (GCP), and company SOPs.
Coordinate and provide reporting data for submissions to regulatory authorities.
Stakeholder Collaboration
Work closely with Clinical Operations, Regulatory Affairs, and Safety teams.
Support cross-functional initiatives within Medical and Clinical Affairs.
Educational Qualifications
Associate’s Degree or equivalent qualification in Life Sciences, Pharmacy, Medicine, or related field. Bachelor’s degree preferred.
Experience Required
Minimum 1–3 years of experience in Medical Affairs, Clinical Research, or Clinical Trial Management within the pharmaceutical or healthcare industry.
Exposure to Phase III and Phase IV clinical studies preferred.
Knowledge of pharmacovigilance and adverse event reporting processes.
Understanding of regulatory submission and compliance requirements.
Core Competencies
Clinical trial oversight and coordination
Investigator engagement and site management
Regulatory compliance and GCP knowledge
Safety monitoring and adverse event reporting
Strong communication and stakeholder management skills
Language Proficiency
Proficiency in English required; regional language proficiency preferred for effective stakeholder engagement in Gujarat.
Why Join Abbott?
Opportunity to contribute to regional clinical excellence initiatives.
Exposure to late-phase clinical trials and investigator-led research.
Career progression within Medical Affairs and Clinical Development functions.
SEO & GEO Keywords: Regional Medical Advisor Jobs Ahmedabad, Medical Affairs Careers Gujarat, Clinical Research Jobs Ahmedabad, Pharma Medical Advisor India, Phase III Phase IV Clinical Trial Jobs Gujarat, Abbott Medical Affairs Jobs India.
This opportunity is suited for early-career medical affairs professionals seeking Regional Medical Advisor roles in Ahmedabad with exposure to clinical trials, investigator engagement, and regulatory compliance within a leading healthcare organization.
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Siliguri |Illinois :
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