Clinical Research Associate (CRA) jobs in India continue to see strong demand as global CROs expand operations across oncology, pharmacovigilance, medical affairs, and clinical development programs. Syneos Health has announced hiring for CRA โ Future Roles (India) in Gurugram with a hybrid working model.
This opportunity is ideal for candidates with experience in clinical monitoring, ICH-GCP compliance, site management, and clinical trial operations who want to build a long-term career in clinical research and pharmaceutical development.
Job Overview
- Role: CRA โ Future Roles (India)
- Company: Syneos Health
- Location: Gurugram
- Work Mode: Hybrid
- Job Type: Full-Time
- Department: Clinical Research / Clinical Operations
- Job Requisition ID: 25106957
Key Responsibilities of Clinical Research Associate (CRA)
Candidates selected for this CRA role at Syneos Health will support clinical trial execution, regulatory compliance, and investigator site management activities across multiple studies.
Major Responsibilities
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure compliance with ICH-GCP, protocol requirements, and SOPs
- Perform Source Document Review (SDR) and verify CRF accuracy
- Monitor patient safety, informed consent, and pharmacovigilance compliance
- Resolve clinical data queries within project timelines
- Support investigator site file (ISF) maintenance and reconciliation with TMF
- Review investigational product (IP) accountability and storage conditions
- Assist with subject recruitment and retention strategies
- Participate in investigator meetings and sponsor discussions
- Maintain audit readiness and support inspection preparation
- Coordinate with project teams, sponsors, and site personnel
- Manage travel-based site monitoring activities across India
For Real World Late Phase studies, selected candidates may additionally support:
- Chart abstraction activities
- Real-world evidence data collection
- Collaboration with local medical and sponsor teams
- Site lifecycle management from startup to closeout
Required Qualifications
Syneos Health is seeking professionals with strong clinical operations and monitoring expertise.
Educational Qualification
- Bachelorโs degree in Life Sciences, Pharmacy, Nursing, or related field
- Registered Nurse (RN) qualification may also be considered
Skills & Experience
- Knowledge of ICH-GCP Guidelines and regulatory requirements
- Experience in clinical trial monitoring and site management
- Strong communication and interpersonal skills
- Ability to work with EDC systems and clinical software tools
- Good documentation and reporting capabilities
- Willingness to travel up to 75%
Why Join Syneos Health Careers
Syneos Health is one of the leading global CROs supporting innovative drug development programs worldwide.
Employee Benefits
- Global clinical research exposure
- Hybrid work flexibility
- Career development and progression programs
- Technical and therapeutic area training
- Inclusive and diverse workplace culture
- Competitive compensation and rewards
- Opportunities across oncology, vaccines, rare diseases, and medical affairs
According to the company, Syneos Health has contributed to:
- 94% of Novel FDA Approved Drugs in recent years
- 95% of EMA Authorized Products
- 200+ studies across 73,000+ sites globally
How to Apply
