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Clinical Research Associate

0-2 years
Not Disclosed
10 Sept. 22, 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

Job Title:

Clinical Research Associate (CRA)

Location: IND-Gurugram
Job ID: 25101768
Updated: September 18, 2025


Company Overview – Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success. The company emphasizes patient-centric clinical development while streamlining processes to ensure efficiency and high-quality outcomes.

Key Highlights:

  • Operates in 110 countries with 29,000 employees.

  • Partnered with 94% of Novel FDA Approved Drugs, 95% of EMA Authorized Products, 200+ studies, 73,000 sites, and 675,000+ trial patients in the last 5 years.

  • Promotes career development, technical training, and peer recognition.

  • Fosters a diverse, inclusive, and authentic workplace through its Total Self culture.

Learn more: Syneos Health


Role Summary

The Clinical Research Associate ensures that clinical research studies are conducted according to widely accepted clinical practices and study protocols. This includes both on-site and remote monitoring, development of monitoring tools, and support of lower-level professionals.


Key Responsibilities

  • Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulations.

  • Develop and implement tools, procedures, and processes to ensure quality monitoring and regulatory adherence.

  • Contribute to the design, implementation, and delivery of clinical monitoring processes, programs, and policies.

  • Collaborate with study teams to ensure accurate and timely data collection, entry, and reporting, resolving discrepancies promptly.

  • Provide guidance, training, and mentoring to junior staff.

  • Manage processes and programs to ensure efficient clinical monitoring operations.

  • Maintain documentation of monitoring activities, findings, and corrective actions.

  • Communicate effectively with study sites, investigators, and stakeholders.

  • Stay current with industry trends, regulatory changes, and best practices in clinical research.

  • Ensure the integrity and quality of clinical data through audits, reviews, and source verification.


Candidate Profile / Skills

  • Education: Bachelor’s degree in life sciences, nursing, or a related field.

  • Experience: Prior experience in clinical research preferred.

  • Certifications: CCRP, CCRA, or other clinical research certifications preferred but not required.

  • Skills:

    • Proficiency in clinical trial management systems and relevant software.

    • Strong analytical, problem-solving, and organizational skills.

    • Excellent communication and interpersonal skills.

    • Attention to detail and ability to maintain high-quality standards.

    • Ability to travel for on-site monitoring as required.

    • Capable of working independently and as part of a team.


Additional Information

  • Tasks listed are not exhaustive; company may assign additional duties.

  • Equivalent skills or experience may be considered in lieu of formal qualifications.

  • Nothing in this description constitutes an employment contract.

  • Syneos Health is committed to ADA compliance and providing reasonable accommodations.


How to Apply

  • Apply directly via Syneos Health website.

  • Not ready to apply? Join the Talent Network to stay connected for future opportunities.