Latest Jobs at Syngene in Bangalore | Life Science Graduates Apply
Syngene International Ltd. is hiring a Clinical Research Associate (CRA) in Bangalore, India. This role offers an exciting opportunity for life science postgraduates with 3–5 years of experience in clinical research to contribute to global drug development. As a CRA, you will play a vital role in site monitoring, study management, and ensuring compliance with ICH-GCP and regulatory standards while collaborating with global pharma and biotech leaders.
- Job Position: Clinical Research Associate (CRA)
- Location: Bangalore, India
- Department: Clinical Operations
About the Company
Syngene International Ltd., founded in 1993, is a leading global discovery, development, and manufacturing organization providing integrated scientific services. With over 4,240 scientists, Syngene partners with top international companies like Bristol-Myers Squibb, Amgen, GSK, Merck KGaA, and Herbalife. Its mission is to accelerate R&D productivity, reduce time to market, and lower the cost of innovation across pharmaceuticals, biotechnology, nutrition, animal health, consumer goods, and specialty chemicals.
Qualifications
Master’s degree in Life Sciences.
Experience
- 3–5 years of core clinical research experience.
- Strong knowledge of ICH-GCP and Indian regulatory guidelines.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Ability to develop SOPs and handle audits.
Job Description
The Clinical Research Associate will liaise with clinical sites and monitor Cliniops studies, ensuring compliance with GCP and regulatory guidelines. The CRA will be responsible for site selection, initiation, monitoring, and close-out visits, while maintaining high standards of quality and integrity in clinical research activities.
Key Responsibilities
- Conduct site selection, initiation, monitoring, and close-out visits as per SOPs and GCP guidelines.
- Manage sites for assigned protocols and therapeutic areas, and ensure compliance.
- Provide training to study sites and maintain regular communication.
- Monitor study progress, including submissions, subject recruitment, CRF completion, and query resolution.
- Document site management activities with reports, letters, and study documentation.
- Support Clinical Project Managers in study design, documentation, and coordination.
- Ensure timely timesheet submissions and delegation of project-level responsibilities.
Skills Required
- Technical Skills: ICH-GCP knowledge, SOP development, MS Office proficiency, and regulatory compliance.
- Behavioral Skills: Strong communication, stress management, empathy, patience, and conflict resolution.
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