Medical Jobs at Qinecsa: Apply Now
Medical Jobs: This opportunity is ideal for doctors looking to advance their careers in pharmacovigilance and drug safety. The Medical Safety Physician will play a critical role in reviewing, assessing, and ensuring the safety of pharmaceutical products across clinical trials, spontaneous reports, and post-marketing surveillance. This role requires strong skills in medical evaluation, regulatory understanding, and case assessment—perfect for MBBS/MD professionals with experience in drug safety, medical review, or clinical practice.
Medical Jobs—About the Company:
Qinecsa Solutions is a global leader in pharmacovigilance and safety sciences, offering advanced technology-enabled services to support the pharmaceutical and life sciences industries. With a strong focus on patient safety, regulatory compliance, and operational excellence, Qinecsa delivers integrated end-to-end drug safety solutions powered by expert medical teams and innovative platforms. The company is known for its collaborative culture, commitment to quality, and dedication to helping partners drive safer, more effective healthcare outcomes.
Medical Jobs—Qualifications:
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Education: MBBS / MD
Experience:
- 1–2 years of experience in Pharmacovigilance (mandatory)
- Minimum 2 years of clinical experience preferred
- Exposure to medical review, regulatory submissions, and safety reporting is desirable.
Role:
The Medical Safety Physician is responsible for ensuring the highest standards of drug safety, medical review, and regulatory compliance across various products and therapeutic areas. The position involves scientific evaluation of Individual Case Safety Reports (ICSRs), assessment of seriousness and causality, MedDRA coding, and collaboration with cross-functional safety teams. This full-time role is well-suited for physicians with hands-on experience in pharmacovigilance and clinical practice who are aiming to build a long-term career in drug safety.
Key Responsibilities:
The Medical Safety Physician will:
- Conduct medical review and assessment of Individual Case Safety Reports (ICSRs) from clinical trials, spontaneous reports, and solicited sources.
- Determine regulatory reportability of cases across assigned products and therapeutic areas in a timely manner.
- Perform triage of cases, assess seriousness, expectedness, and causality.
- Review and verify correct identification of adverse events from source documents, with accurate MedDRA coding.
- Assess case narratives, labeling, and clinical consistency across reports.
- Maintain updated knowledge of product portfolios, safety profiles, and relevant therapeutic areas.
- Escalate complex or high-risk cases to senior medical review teams, as required.
- Review litigation cases and provide safety-related medical input across products.
- Identify, troubleshoot, and resolve case processing or data discrepancies.
- Coordinate with internal teams and client safety teams for case clarifications or product-specific issues.
- Communicate effectively with cross-functional teams, including clinical, regulatory, and safety specialists.
- Stay updated with global Health Authority regulations (e.g., FDA, EMA, MHRA).
- Perform any additional drug safety activities allocated by the pharmacovigilance leadership team.
