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Clinical Research Associate

0-2 years
Not Disclosed
10 Sept. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

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