Clinical Research Job at Syngene
Looking for a high-growth Clinical Research Job in India? This exciting opportunity at Syngene offers a dynamic role for experienced professionals eager to advance as a Clinical Research Associate. If you’re passionate about clinical trials, regulatory compliance, and patient safety, this role provides the perfect platform to enhance your career in the life sciences domain.
About the Company
Syngene International Ltd is an innovation-led contract research, development, and manufacturing organization that provides integrated scientific services from early discovery to commercial supply. The company emphasizes safety, quality, and integrity across all its operations.
Job Details:
- Job Title: Senior Clinical Research Associate (Sr. CRA)
- Location: Bangalore, India
- Company: Syngene International Ltd
- Division: Discovery Services
- Department: Clinical Operations – T&CR
Role Overview
The Senior Clinical Research Associate (Sr. CRA) is responsible for managing clinical trial sites and ensuring studies are conducted in compliance with protocols, regulatory guidelines, and Good Clinical Practice (GCP). The role involves end-to-end site management including initiation, monitoring, and close-out activities.
Core Responsibilities
- Perform site selection, initiation, monitoring, and close-out visits
- Manage assigned clinical trial sites, protocols, and therapeutic areas
- Ensure compliance with Standard Operating Procedures (SOPs) and GCP guidelines
- Conduct protocol and study-related training for site personnel
- Maintain effective communication with clinical trial sites
- Ensure quality and integrity of data collected at site level
- Identify and resolve quality issues in collaboration with Clinical Project Manager
- Track regulatory submissions, ethics approvals, and subject recruitment
- Oversee case report form (CRF) completion and data query resolution
Role Accountabilities
- Maintain accurate documentation of site management and monitoring activities
- Submit monitoring visit reports and follow-up communications
- Ensure timely submission of timesheets and project-related documentation
Safety & Compliance Expectations
- Adhere to all environment, health, and safety (EHS) protocols
- Ensure compliance with company quality standards and data integrity practices
- Participate in safety training and promote a safety-first culture
- Monitor and review safety metrics regularly
- Ensure team adherence to safety and compliance requirements
Candidate Profile
The ideal candidate is an experienced clinical research professional with strong site management skills and the ability to work in a fast-paced, regulated environment.
Educational Qualification
- M.Sc. Life Sciences degree
Experience
- Prior experience as a Senior Clinical Research Associate (Sr. CRA)
Key Skills & Competencies
- Strong communication and interpersonal skills
- Ability to work in dynamic and ambiguous environments
- Time management and ability to meet tight deadlines
- Problem-solving and innovative thinking
- Strong focus and attention to detail
- Team collaboration and coordination
Core Values
- Excellence
- Integrity
- Professionalism
Work Environment
- Clinical operations role with site visits and coordination responsibilities
- High focus on compliance, quality, and safety
- Collaborative and performance-driven environment
