Clinical Research Associate (CRA) – Syneos Health
Location: Gurugram, India
Job ID: 25101768
Updated: September 18, 2025
About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. Our Clinical Development model places patients and customers at the center of everything we do, focusing on innovative, streamlined solutions for modern clinical trials.
Employees: 29,000 across 110 countries
Experience: Involved with 94% of Novel FDA-approved drugs, 95% of EMA-authorized products, 200+ studies, 73,000 sites, and 675,000+ trial patients.
Culture: Total Self culture fostering diversity, authenticity, career growth, and inclusion.
Job Overview
The CRA (P20 level) ensures that clinical research studies are conducted according to accepted clinical practices and regulatory requirements. Responsibilities include on-site and remote monitoring, quality assurance, and supporting the professional growth of lower-level professionals.
Key Responsibilities
Clinical Monitoring & Compliance:
Conduct comprehensive on-site and remote monitoring of clinical trials.
Ensure compliance with study protocols, regulations, and GCP guidelines.
Perform audits, source data verification, and data quality checks.
Process Development & Implementation:
Develop and implement tools, procedures, and processes for effective monitoring.
Contribute to design, implementation, and delivery of monitoring processes, programs, and policies.
Collaboration & Guidance:
Work with study teams to ensure accurate, timely data collection and reporting.
Provide training, guidance, and mentorship to lower-level professionals.
Communicate effectively with study sites, investigators, and other stakeholders.
Continuous Learning & Improvement:
Stay current with industry trends, regulatory updates, and best practices.
Identify opportunities to streamline processes and improve efficiency.
Qualifications
Education: Bachelor’s degree in life sciences, nursing, or related field.
Experience: Previous clinical research experience preferred.
Skills:
Strong understanding of clinical trial processes and regulations
Excellent organizational, analytical, and problem-solving skills
Effective communication and interpersonal skills
Attention to detail and high standards of quality
Ability to work independently and as part of a team
Certifications (preferred): CCRP, CCRA, or other clinical research certifications
Technical Requirements
Proficiency with clinical trial management systems and relevant software
Willingness to travel for on-site monitoring
Impact & Contribution (P20 Level)
Ensures trial integrity and quality through rigorous monitoring
Develops tools, procedures, and processes to enhance efficiency
Supports and mentors junior staff
Manages specific processes and programs within the clinical monitoring function
Additional Information
Tasks and responsibilities may vary at the company’s discretion
Equivalent experience or skills may be considered
Commitment to diversity, inclusion, and accommodations under ADA
Expressing interest adds you to Syneos Health’s talent pipeline for upcoming opportunities
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