Corporate Medical Affairs Specialist at Parexel (Remote, India)
Remote · Full Time
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- Experience
- 2+ yrs
- Salary
- —
- Openings
- 1
- Posted
- 3 days ago
- Work mode
- Work from home
- Education
- MBBS or MD
- Eligibility
- Medical professionals with MBBS or MD degrees, particularly those with pharmacovigilance and medical monitoring experience; candidates should have completed basic clinical training such as internship or residency.
- Resume
- Required to apply
Job description
Overview
Parexel is seeking dedicated medical professionals to join its Corporate Medical Affairs team, contributing to patient safety and the advancement of drug development. This remote position based in India offers a chance to be part of a trusted global leader in biopharmaceutical services committed to regulatory adherence and superior service quality.
About Parexel
Parexel is an established global provider specializing in the healthcare and biopharmaceutical sectors, delivering comprehensive solutions with a focus on enhancing drug safety and development processes. Operating globally, including in India, the company emphasizes regulatory compliance and quality medical affairs services.
Job Details & Responsibilities
- Monitor and maintain detailed knowledge of adverse event and safety profiles related to assigned pharmaceutical products.
- Ensure compliance with internal and external regulatory timeframes for adverse event reporting.
- Collaborate and communicate effectively with internal teams and external stakeholders to resolve pharmacovigilance issues.
- Participate actively in client meetings and cross-disciplinary team discussions.
- Support audit and inspection processes as part of quality assurance and compliance.
- Provide mentorship and guidance to junior physicians engaged in patient safety roles.
- Conduct detailed medical reviews of complex individual case safety reports (ICSR) and provide expert medical input to case processing teams.
- Identify, evaluate, and resolve any medical case issues that arise.
Qualifications & Eligibility
- Graduate with MBBS or MD degree from a recognized medical institution.
- Minimum two years of experience reviewing Individual Case Safety Reports (ICSR) within pharmacovigilance or related functions.
- Solid understanding of medical terminology and clinical practice.
- Experience or familiarity with pharmacovigilance, drug safety, or clinical medicine is preferred.
- Completion of basic clinical internship or residency training.
- Prior experience in medical monitoring and pharmacovigilance is advantageous.