Auriga Research is hiring a Clinical Trial Associate (CTA) in New Delhi for candidates with a background in pharmacy and clinical research. The position involves clinical trial documentation, Investigator Site File maintenance, patient recruitment coordination, data query follow-up, and support for clinical monitoring activities.
Job Details
| Particulars | Details |
|---|---|
| Company | Auriga Research |
| Job Title | Clinical Trial Associate (CTA) |
| Job Location | New Delhi |
| Experience | 2–3 years |
| Salary | ₹3–4 LPA |
| Employment Type | Full-time, Permanent |
| Department | Research & Development |
| Industry | Clinical Research / Contract Research |
| Qualification | B.Pharm / M.Pharm |
| Openings | 1 |
Position: Clinical Trial Associate
The Clinical Trial Associate will support clinical study documentation, site coordination, data query resolution, and administrative activities under the supervision of Clinical Research Associates (CRAs).
Key Responsibilities
- Maintain study documentation and organise Investigator Site Files (ISFs).
- Assist with basic Case Report Form (CRF) completion reviews for assigned studies.
- Coordinate patient recruitment activities and maintain screening logs under CRA supervision.
- Learn documentation requirements for pharmaceutical, medical device, and AYUSH/nutraceutical studies.
- Shadow senior CRAs during site initiation, monitoring, and close-out visits.
- Support routine data query resolution and maintain follow-up documentation.
- Assist with courier tracking, clinical trial supply management, and meeting scheduling.
- Maintain accurate records of training completion and site-specific requirements according to study protocols.
Eligibility and Qualifications
Candidates applying for the Clinical Trial Associate position should meet the following requirements:
- B.Pharm or M.Pharm graduate.
- Up to 2–3 years of relevant clinical research experience.
- Exposure to site coordination and clinical trial documentation practices.
- Experience or exposure across approximately 4–5 studies through academic work, internships, or professional experience.
- Basic understanding of Good Clinical Practice (GCP) principles.
Required Skills
The job description highlights the following skills and areas of knowledge:
- Clinical research and clinical operations
- Clinical trial documentation
- Investigator Site File (ISF) maintenance
- Case Report Form (CRF) review
- Site coordination and site monitoring
- Clinical monitoring support
- ICH-GCP principles
- Clinical Research Associate (CRA) and Clinical Research Coordinator (CRC) processes
- Medical device and cosmetic trials
- Oncology clinical trials
About Auriga Research
Auriga Research is a Contract Research Organization (CRO) conducting regulated Phase II–IV clinical trials across India. According to the company information provided, its clinical operations are supported by a network of 370 investigator sites and more than 100 Site Management Organization (SMO) partnerships.
The company states that its clinical trial operations follow ICH E6(R3) Good Clinical Practice and the New Drugs and Clinical Trials Rules, 2019. Its facilities also include a bioanalytical laboratory with NABL and USFDA inspection credentials.