Clinical Research Associate Jobs | Syngene is Hiring | Apply Now
Looking to build a strong foundation in clinical research with a globally trusted organization? Syngene career opportunities bring an exciting opening for Clinical Research Associate jobs in Bangalore. This role is ideal for postgraduates seeking meaningful life science jobs where science meets real-world clinical impact through global research collaborations.
Job Details
- Job Title: Clinical Research Associate
- Location: Bangalore
About the Company
Syngene International Ltd., incorporated in 1993, is a globally recognized innovation-driven organization providing integrated discovery, development, and manufacturing services. The company partners with leading pharmaceutical and biotechnology giants worldwide. With a strong scientific workforce, Syngene supports cutting-edge research while offering rewarding life science jobs for professionals aiming to grow in clinical and translational research.
Key Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits in accordance with contracted scope of work, Standard Operating Procedures, and all the applicable Good Clinical Practice (GCP) Guidelines and Regulations.
- Responsible for site management for the assigned protocols, sites, and therapeutic areas.
- Complete appropriate Standard Operating Procedure training, therapeutic area training, protocol training, and any relevant training required to perform job duties.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and activities.
- Ensure the quality and integrity of study conducted at site level in accordance with protocol and applicable regulations. Investigate and discuss quality issues with Clinical Project Manager for resolution and implementation of Corrective Action and Preventive Action.
- Manage the progress and performance of the assigned study sites by following activities but not limited to: tracking regulatory and Ethics Committee submissions and approvals, subject recruitment, case report form (CRF) completion and submission, and data query generation and resolution.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans by submitting regular visit reports, generating follow-up letters, and other required study documentation.
- Provide assistance to the Clinical Project Manager with design of study tools, documents, and processes.
- Timely submission of timesheets for Project-specific and other tasks.
- Supporting the Clinical Project Manager for coordination within the project team.
- Delegation of project-level Clinical Project Manager responsibilities.
Educational Qualification
Masters Degree in Life Science
Technical/functional Skills
- Sound knowledge on ICH-GCP and Indian Regulatory guidelines.
- Well-versed with Microsoft Office documents (MS Word, Excel, PowerPoint).
- Knowledge about developing SOPs.
- Well-versed with facing internal and external audits.
Experience
Experience in core clinical research activities within clinical research.
Behavioral Skills
Proficient in English (reading and writing), Stress Management, Empathy, Conflict resolution, and Patience.
This opportunity is ideal for candidates aspiring to establish a long-term Syngene career in clinical research. These Clinical Research Associate jobs offer hands-on exposure, global project experience, and a strong professional learning environment, making it a valuable step for postgraduates exploring impactful life science jobs.
