We are hiring for Leading Clinical Research Organisation

Role: Clinical Research Associate

Experience: min 3 Years

Reporting To: Head Project Management / Clinical Trial Lead

Location: Chennai

NOTE- Candidate should be willing to relocate Chennai

Key Responsibilities

Clinical monitoring and site management

- Conduct Site Qualification, Initiation, Monitoring and Close-Out Visits (SQV, SIV, IMV, COV), independently for assigned activities following training and study authorisation.

- Perform source data review and verification (SDR/SDV) and assess protocol compliance, data quality and participant safety.
- Review essential documents and maintain inspection-ready site files.

• Prepare accurate monitoring reports and follow-up communications within agreed timelines; track site issues, protocol deviations and data queries through resolution. Site performance and study execution

- Support site activation, enrolment, retention and study close-out activities.
- Monitor site performance and support enrolment improvement initiatives.
- Identify and escalate operational risks and site-related challenges.

Investigator and stakeholder management

- Build and maintain robust relationships with investigators and site personnel.




- Serve as the primary operational contact for assigned sites.
- Participate in investigator meetings, study team meetings and site training.

Cross functional collaboration and compliance

- Collaborate with Clinical Operations, Data Management, Safety, Regulatory, Medical Writing and external vendors.
- Ensure compliance with ICH-GCP, protocol requirements and applicable regulations.
- Support sponsor audits, inspections and inspection readiness activities

Skills and competencies

- Strong understanding of ICH-GCP and clinical trial regulations.
- Strong monitoring, site management and investigator relationship management skills
- Effective communication, stakeholder management and problem-solving abilities. • Ability to work independently and within cross-functional global teams.
- Willingness to travel as required

Preferred experience

- Experience in global Phase II and Phase III clinical trials.
- Exposure to sponsor audits, inspections and co-monitoring visits.
- Demonstrated potential to progress into CRA II and Senior CRA roles.

Interested Candidates can share there CV at [email protected] or Whatsapp- (phone hidden)

Regards

Nupur Tathe

(HR Recruiter)

Pace HR Consulting LLP

📌 Clinical Research Associate (Chennai)
🏢 Pace Hr Consulting
📍 Chennai