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Cra – Future Roles (India)

Syneos Health
1-3 years
₹5–8 LPA
Gurgaon, Gurugram, India
10 July 2, 2026
Job Description
Job Type: Full Time, Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Job Title: CRA – Future Roles (India)

Company: Syneos Health

Location: Gurugram, India (Hybrid)

Employment Type: Full-time

Job Requisition ID: 25106957

Overview:
Syneos Health is building a talent pipeline for future Clinical Research Associate (CRA) opportunities in India. The CRA will be responsible for monitoring clinical trial sites, ensuring compliance with ICH-GCP guidelines, regulatory requirements, study protocols, and maintaining the quality and integrity of clinical trial data.

Required Qualifications:

  • Bachelor's degree in Life Sciences, Pharmacy, Nursing (RN), or a related field.

  • Knowledge of ICH-GCP Guidelines and applicable regulatory requirements.

  • Good computer proficiency and ability to learn new technologies.

  • Excellent communication, presentation, and interpersonal skills.

  • Willingness to travel up to 75% as required.

Experience:

  • 1–3 years of relevant experience in Clinical Research or Clinical Trial Monitoring. Candidates with relevant internship or clinical research exposure may also be considered for future opportunities.

Salary Criteria:

  • Expected Salary: ₹5–8 LPA (CTC), depending on qualifications, relevant experience, and interview performance.

Key Responsibilities:

  • Conduct site qualification, initiation, monitoring, management, and close-out visits (on-site and remote).

  • Ensure compliance with ICH-GCP, regulatory guidelines, study protocols, and company SOPs.

  • Verify informed consent, patient safety, protocol adherence, and data integrity.

  • Perform source document verification (SDV) and review case report forms (CRFs).

  • Resolve data queries and ensure timely closure.

  • Monitor investigational product (IP) accountability, storage, reconciliation, and documentation.

  • Maintain Investigator Site Files (ISF) and reconcile with Trial Master Files (TMF).

  • Prepare monitoring reports, follow-up letters, and other study documentation.

  • Coordinate with investigators, site staff, sponsors, and project teams.

  • Support subject recruitment, retention, audit readiness, and regulatory inspections.

  • Participate in investigator meetings, sponsor meetings, and clinical training sessions.

  • Support Real World Late Phase studies, including site management and chart abstraction activities, where applicable.

Working Hours:

  • As per project requirements.

Work Mode:

  • Hybrid

Travel Requirement:

  • Up to 75% travel based on project needs.

Important Note:

  • This is a future opportunity (Talent Pipeline) and not an active hiring position. Interested candidates will be considered when suitable CRA roles become available.

Equal Employment Opportunity:
Syneos Health is an equal opportunity employer committed to fostering a diverse and inclusive workplace and providing equal employment opportunities to all qualified candidates.