Medical Review Physician Job Vacancy at ClinChoice – MBBS & MD Job Opportunities | Apply Now
ClinChoice is hiring for a Medical Review Physician job vacancy, offering a rewarding career path for MBBS and MD graduates. This role involves high-quality medical review of ICSRs across multiple therapeutic areas, ensuring compliance with GVP modules and international regulatory guidelines. Ideal candidates will gain hands-on experience, mentoring opportunities, and exposure to diverse MBBS and MD job opportunities in pharmacovigilance.
Job Position: Medical Review Physician 1
About the Company:
ClinChoice is a leading global provider of pharmacovigilance and clinical research services. The company delivers high-quality safety solutions across multiple therapeutic areas, helping clients comply with international regulations and ensuring patient safety worldwide. This is an ideal place for MBBS and MD graduates seeking rewarding job opportunities in the field.
Qualifications:
- MBBS/MD with 2-4 years of experience as a Medical Reviewer for ICSRs.
- Strong knowledge of ICH-GCP, relevant GVP modules, 21 CFR guidelines, and other regulatory requirements.
- Training and mentoring skills in GVP concepts, disease conditions, and product portfolios.
- Proficiency in MS Office applications, including Outlook, Excel, Word, and PowerPoint.
Job Description:
The Medical Review Physician job vacancy at ClinChoice requires reviewing ICSRs with precision, ensuring regulatory compliance, and providing expert guidance to case processors. The role allows MBBS and MD professionals to grow in pharmacovigilance while participating in process improvements and mentoring initiatives.
Key Responsibilities:
- Perform medical review of ICSRs from multiple sources including Spontaneous, Literature, Regulatory Authority, Solicited, and Clinical trials.
- Assess the seriousness, expectedness, causality, and narrative of adverse events without compromising on quality and compliance.
- Assign appropriate MedDRA coding, assess labeling, and review narratives.
- Support case triage and determine relatedness across products.
- Maintain knowledge of product portfolios and safety profiles across therapeutic areas like Oncology, Respiratory, Immunology, Neuroscience, and Rare Diseases.
- Provide medical guidance and mentorship to case processors and quality reviewers.
- Identify and resolve case issues, coordinating with client teams and internal stakeholders.
- Contribute to process improvement initiatives while maintaining compliance with international safety regulations.
- Complete medical review activities within stipulated timelines to meet SLAs and regulatory requirements.
- Assist in training and mentoring new team members.
- Perform ad-hoc tasks as directed by team leads/managers.
