A hospital group’s shared back-office team is hiring a Clinical Research Associate (CRA) for its clinical operations team through Flexiple. The team supports four hospitals and manages investigator-led and sponsored clinical studies.
The position is based on-site in Delhi or Hyderabad. Candidates with 2 to 6 years of experience in clinical trial monitoring or clinical operations can apply.
Job Details
| Particulars | Details |
|---|---|
| Hiring Platform | Flexiple |
| Job Role | Clinical Research Associate (CRA) |
| Job Type | Full-Time |
| Job Locations | Delhi / Hyderabad |
| Work Mode | On-site |
| Experience | 2–6 Years |
| Qualification | Bachelor’s / Master’s Degree |
| Relevant Fields | Life Sciences, Pharmacy, Medicine |
| Department | Clinical Operations |
| Reporting To | Clinical Project Manager |
| Placement | Intended to be Long-Term |
Position
Clinical Research Associate (CRA)
The selected candidate will monitor clinical trial sites, ensure compliance with study protocols and Good Clinical Practice (GCP), verify clinical trial data, and maintain accurate study documentation.
The role involves supporting hospital site teams conducting investigator-led and sponsored clinical studies.
Key Responsibilities
- Conduct site initiation, site monitoring, and site close-out activities.
- Verify clinical trial data against source documents and resolve data queries.
- Ensure compliance with clinical study protocols, ICH-GCP, and local regulations.
- Review informed consent and safety-reporting processes.
- Maintain Trial Master File (TMF) documentation and site files.
- Prepare clinical monitoring visit reports and follow up on action items.
- Support investigators and site staff through training and clinical research-related guidance.
Eligibility and Qualifications
Candidates should meet the following requirements:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or Medicine.
- 2 to 6 years of experience in clinical trial monitoring or clinical operations.
- Previous experience in clinical monitoring or clinical operations.
- Working knowledge of ICH-GCP and Indian clinical-trial regulations.
- Willingness to travel to clinical trial sites.
Required Skills
- Clinical Trial Monitoring
- Site Initiation, Monitoring and Close-Out
- ICH-GCP Compliance
- Source Data Verification (SDV)
- Clinical Data Query Resolution
- Informed Consent Review
- Safety Reporting
- Trial Master File (TMF) Management
- Monitoring Visit Report Preparation
- Clinical Site Coordination
Additional Preferred Skills
Candidates with the following experience will have an added advantage:
- Experience with Electronic Trial Master File (eTMF) systems.
- Experience with Electronic Data Capture (EDC) systems.
- Therapeutic experience in Oncology, Cardiology, or Diabetes.
- Formal GCP certification.
Clinical Research Associate Hiring Process
The provided job listing describes the following hiring stages:
- Screening Call
- Assignment
- Team Panel
- Final Fit Conversation
The platform also lists a seven-stage hiring process:
- Internal HM Review
- Flexiple Interview
- Profile Review
- Technical Interview 1
- Technical Interview 2
- Technical Interview 3
- Founder Interview
