Medical Job at Syngene | Jobs in Bangalore
This Medical Job at Syngene offers an excellent opportunity for licensed physicians seeking jobs in Bangalore within clinical research and patient safety oversight. Based in Bengaluru, Karnataka, this role supports translational and clinical research projects while ensuring regulatory compliance, scientific integrity, and participant safety across multiple therapeutic areas.
Job Details
- Job Title: Medical Monitor
- Division: Discovery Services
- Department: Medical & Regulatory Affairs
- Operating Unit: Translational and Clinical Research
- Job Location: Bengaluru, Karnataka
About the Company
Syngene represent opportunities at an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply. For professionals searching for a medical job in Bangalore, Syngene provides a strong safety-first culture where operational excellence and patient well-being are equally prioritized.
Qualifications
- Education: MBBS, MD Pharmacology
- Experience: Foundational
Medical Job Description
This Medical Job at Syngene Careers focuses on patient safety oversight in clinical trials. The Medical Monitor role involves continuous evaluation of participant well-being, medical review of adverse events, and regulatory compliance. This opportunity is ideal for professionals exploring jobs in Bangalore within translational and clinical research environments.
Core Purpose of the Role
- Patient safety oversight through continuous evaluation of adverse events and serious adverse events
- Ensuring scientific integrity and accurate medical decision-making
- Providing expert medical guidance during clinical study design and execution
- Enhancing research quality through ongoing data review
- Maintaining regulatory and ethical compliance in line with ICH-GCP guidelines
Medical Job – Key Responsibilities
- Associate Research Physician in clinical trial-related projects across therapeutic areas
- Medical review and interpretation of clinical and safety data
- Preparation and review of protocol-related regulatory documents
- Review of MedDRA and WHO Drug Insight coding
- Support in SAE narrative preparation and quality analysis
- Communication of SAEs to stakeholders as per internal SOPs
- Drafting Integrated Summary of Safety and Efficacy documents
- Review of clinical protocols and study synopses
- Preparation of Medical Monitoring Plans and Safety Management Plans
- Training study teams and resolving protocol-related queries
- Managing regulatory documentation and timelines
- Travel within India for site monitoring activities
