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Regional Medical Advisor

Abbott
Abbott
1+ years
Not Disclosed
Ahmedabad, India
10 Feb. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Regional Medical Advisor – Medical and Clinical Affairs

Job Location
Ahmedabad, India

Job Category
Medical and Clinical Affairs

Employment Type
Full-Time

Experience Required
Minimum 1+ year of relevant experience in Medical Affairs, Clinical Research, or Clinical Trials Management

Education Requirement
Associate Degree or equivalent qualification in Life Sciences, Pharmacy, Medicine, Clinical Research, or related healthcare discipline


Job Overview

The Regional Medical Advisor will play a critical role in supporting medical and clinical affairs operations by overseeing clinical research activities, implementing clinical protocols, and ensuring regulatory compliance. This position requires an experienced professional with strong expertise in clinical trial management, data collection processes, and investigator coordination.

The role involves directing clinical trial activities, supporting regulatory submissions, monitoring study execution, and ensuring adherence to established clinical and ethical standards. The candidate will collaborate with internal teams, clinical investigators, and regulatory authorities to ensure successful execution of clinical research initiatives.


Key Responsibilities

  • Provide strategic direction, planning, and execution support for clinical trials, research activities, and data collection processes.

  • Contribute to the implementation and management of clinical study protocols and facilitate preparation of final clinical reports.

  • Recruit clinical investigators and negotiate study design, timelines, and budgets.

  • Direct and manage Phase III and Phase IV human clinical trials for company products under development.

  • Monitor clinical trial progress to ensure compliance with study protocols and regulatory requirements.

  • Participate in adverse event reporting and safety monitoring activities.

  • Coordinate preparation and submission of clinical reports to regulatory authorities.

  • Oversee investigator initiation activities and manage group study operations.

  • Act as a liaison or consultant with partner organizations under licensing or collaboration agreements when required.

  • Ensure study completion and maintain adherence to ethical and clinical standards throughout the research lifecycle.


Required Qualifications and Skills

  • Associate Degree or equivalent qualification in Life Sciences, Clinical Research, Pharmacy, Medicine, or a related healthcare field.

  • Minimum 1 year of professional experience in Medical Affairs, Clinical Research, or Clinical Trial Management.

  • Knowledge of clinical trial processes, regulatory requirements, and safety reporting procedures.

  • Understanding of clinical protocol development and research methodologies.

  • Strong analytical, coordination, and documentation skills.

  • Ability to collaborate with investigators, regulatory authorities, and cross-functional teams.

  • Effective communication and stakeholder management capabilities.


Language Proficiency

  • Professional proficiency in English required.

  • Additional regional language proficiency is considered an advantage.