Explore exciting pharma jobs at Syngene International. Medical Monitor role in clinical trials offering opportunities in Bengaluru for MBBS/MD professionals in pharmaceutical careers in India.
Contents
About the Company
Syngene International Limited is an innovation-led contract research, development, and manufacturing organization (CRDMO). It provides integrated scientific services from early discovery through commercial supply.
A subsidiary of Biocon, Syngene operates with a strong focus on safety, quality, regulatory compliance, and scientific excellence. With global clients and cutting-edge facilities, it is a trusted partner driving advancements in healthcare and a top choice for pharmaceutical careers in India.
Job Details
- Company Name: Syngene International Limited
- Experience: Entry-level (For Freshers)
- Qualification: MBBS with MD Pharmacology
- Location: Bengaluru, Karnataka, India
- Work Type: On-site
Job Description
Syngene is hiring a Medical Monitor to join its Translational and Clinical Research team in Bengaluru. This clinical trials role offers physicians the opportunity to ensure patient safety, scientific integrity, and regulatory compliance in innovative research projects.
Join a dynamic organization committed to excellence and patient-centric clinical development.
Medical Monitor
- Department: Medical & Regulatory Affairs
- Operating Unit: Translational and Clinical Research
- Division: Discovery Services
- Role: Provide medical oversight, safety monitoring, and expert guidance in clinical trials across therapeutic areas
- Experience: Foundational level
- Education/Qualification: MBBS with MD Pharmacology
Skills/Qualifications
- MBBS with MD in Pharmacology
- Strong clinical knowledge in medicine, pharmacology, and relevant therapeutic areas
- Expertise in evaluating adverse events (AEs) and serious adverse events (SAEs)
- In-depth understanding of ICH-GCP guidelines and local regulatory requirements
- Proven skills in clinical data interpretation and safety signal detection
- Excellent communication for clear medical insights to diverse stakeholders
- Strong problem-solving, leadership, and cross-functional collaboration abilities
- Commitment to ethical standards and patient welfare
Key Responsibilities
- Ensure patient safety through ongoing adverse event review
- Provide medical interpretation of clinical and safety data
- Support protocol development and review of key documents
- Generate SAE narratives and safety summaries
- Prepare Medical Monitoring Plans and Risk Mitigation Strategies
- Review MedDRA/WHO Drug coding when required
- Train study teams and address protocol queries
- Conduct site monitoring visits within India as needed
Benefits/Perks
- Competitive salary and comprehensive benefits
- Strong focus on safety, learning, and professional growth
- Exposure to global clinical research projects
- Collaborative and innovation-driven work culture
- Opportunities for leadership and cross-functional development
- Commitment to work-life balance and employee well-being
How to Apply
Interested candidates should apply through the official Syngene careers portal at https://www.syngeneintl.com/careers. Submit your updated resume highlighting relevant clinical and regulatory experience.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Syngene LinkedIn page.
For more pharma job opportunities and guidance on pharmaceutical careers in India, visit https://pharmarecruiter.in. Apply now and advance your career in clinical research with Syngene!
Why You Should Join
Syngene embodies excellence, integrity, and professionalism while placing safety at the core of its operations. Employees enjoy a supportive environment that promotes continuous learning, ethical leadership, and meaningful contributions to global healthcare.
With a strong emphasis on regulatory compliance, innovation, and employee accountability, Syngene offers long-term career stability and growth in a world-class CRDMO setting.
FAQs
What qualifications are required for the Medical Monitor role at Syngene?
Candidates must hold MBBS with MD in Pharmacology; foundational experience is sufficient.
Is this Medical Monitor position open to fresh MD graduates?
Yes, the role welcomes candidates with foundational-level experience in clinical research.
Where is the job location for this Syngene clinical trials role?
The position is based in Bengaluru, Karnataka, with possible travel to study sites in India.
What career growth opportunities does Syngene offer?
Syngene provides competitive compensation, global exposure, leadership development, and a strong focus on safety and professional excellence. Explore more at https://pharmarecruiter.in.