Syneos Health Hiring Senior Clinical Research Associate – Apply Now!
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- Syneos Health Hiring Senior Clinical Research Associate – Apply Now!
- About Syneos Health
- Job Overview – Senior Clinical Research Associate (CRA II / Sr CRA)
- Key Responsibilities
- Clinical Site Management & Monitoring
- Regulatory & Compliance Oversight
- Data & Documentation Management
- Collaboration & Communication
- Required Qualifications
- How to Apply
Syneos Health Hiring Senior Clinical Research Associate – Apply Now!
About Syneos Health
Syneos Health is a globally recognized biopharmaceutical solutions organization, dedicated to accelerating the delivery of innovative therapies to patients worldwide. With over 29,000 employees across 110 countries, Syneos Health provides comprehensive clinical development services, ensuring high-quality research and streamlined operations.
If you’re passionate about clinical research and looking for a rewarding career, Syneos Health is the place for you!
Job Overview – Senior Clinical Research Associate (CRA II / Sr CRA)
Current Openings:
- Position: CRA II / Sr CRA
- Location: Mumbai, Delhi, Bangalore, Hyderabad (Client-Based)
- Experience Required: Minimum 4 years in clinical research, with oncology and cardiovascular therapeutic area experience preferred
- Qualification: Bachelor’s degree or RN in a relevant field
- Travel: Up to 75% (as required)
Key Responsibilities
Clinical Site Management & Monitoring
- Conducts site qualification, initiation, routine monitoring, and close-out visits, ensuring compliance with regulatory standards and study protocols.
- Performs Source Document Verification (SDV) and ensures the accuracy of case report forms (CRFs).
- Evaluates patient safety and site compliance with study requirements.
- Reviews and reconciles the Investigator Site File (ISF) with the Trial Master File (TMF).
Regulatory & Compliance Oversight
- Ensures adherence to ICH-GCP, Good Pharmacoepidemiological Practices (GPP), and local regulatory guidelines.
- Conducts audits to verify the accuracy of informed consent documentation.
- Provides guidance to site personnel for audit readiness and regulatory compliance.
Data & Documentation Management
- Reviews investigational product (IP) inventory, storage, and security compliance.
- Ensures accurate data entry in electronic data capture systems and resolves queries efficiently.
- Documents all activities in trip reports, follow-up letters, and monitoring logs.
Collaboration & Communication
- Acts as the primary liaison between Syneos Health, site personnel, and study sponsors.
- Supports recruitment and retention efforts to enhance study enrollment.
- Attends Investigator Meetings, sponsor visits, and clinical training sessions as required.
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Required Qualifications
- Minimum Experience: At least 4 years in clinical research, with a preference for oncology and cardiovascular experience.
- Educational Background: Bachelor’s degree in Life Sciences (Biotechnology, Microbiology, Biochemistry, Genetics, Molecular Biology), Nursing (BSc Nursing, MSc Nursing), Pharmacy (BPharm, MPharm, PharmD), or an equivalent field such as Clinical Research, Public Health, or Medical Laboratory Sciences.
- Technical Skills: Knowledge of ICH-GCP, regulatory requirements, and electronic data capture systems.
- Soft Skills: Strong communication, problem-solving, and analytical abilities.
- Flexibility: Willingness to travel up to 75% as per project requirements.
How to Apply
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📱 Get More DetailsIf you meet the qualifications and are ready to advance your career in clinical research, apply now! Click the link below to submit your application:
To apply for this job please visit www.syneoshealth.com.