REV Clinical Hiring 2026 – Junior Clinical Research Associate in Ahmedabad
Are you a M.Pharm, Pharm.D or Life Sciences graduate looking to begin your career in clinical research?
REV Clinical is hiring for a Junior Clinical Research Associate / Clinical Trial Assistant position in Ahmedabad. The role is designed for freshers and early-career professionals who want to gain practical experience in clinical trial operations, study start-up and regulatory documentation.
The position is office-based and full-time, with candidates working alongside experienced clinical research teams.
About REV Clinical
REV Clinical is a global Clinical Research Organization (CRO) headquartered in the United States, with operations in Australia and India.
The organization works across therapeutic areas including:
- Oncology
- Neurology
- Ophthalmology
- Rare Diseases
Its services cover areas such as clinical trial design, regulatory submissions, biometrics, data management, quality compliance and clinical trial support.
Job Overview
| Details | Information |
|---|---|
| Company | REV Clinical |
| Position | Junior Clinical Research Associate / Clinical Trial Assistant |
| Department | Clinical Operations / Clinical Trial Support |
| Location | Ahmedabad, Gujarat |
| Experience | 0–1 years |
| Qualification | M.Pharm / Pharm.D / Life Sciences |
| Work Type | On-site |
| Employment Type | Full-time |
| CRC Experience | Preferred |
Junior Clinical Research Associate – Job Role
The Junior Clinical Research Associate / Clinical Trial Assistant will support clinical trial start-up and operational activities.
This entry-level position involves working with study documentation, site feasibility, regulatory submissions and project tracking.
It can be suitable for candidates who want to develop their career in clinical operations, clinical trial management and regulatory coordination.
Eligibility Criteria
Candidates should have:
- M.Pharm
- Pharm.D
- Degree in Life Sciences
- 0–1 years of relevant experience
- Clinical Research Coordinator (CRC) experience is preferred
- Basic understanding of clinical trial processes
- Understanding of regulatory documentation and requirements
- Good organizational and documentation skills
- Strong communication and coordination abilities
- Ability to manage multiple tasks and timelines
Fresh graduates with the required educational background can consider this opportunity.
Skills Required
The role requires a combination of clinical research knowledge and organizational skills.
Important skills include:
- Basic knowledge of clinical trial operations
- Understanding of study start-up activities
- Familiarity with regulatory documentation
- Awareness of Ethics Committee submissions
- Basic understanding of DCGI submission procedures
- Strong documentation skills
- Good coordination and communication
- Time management
- Attention to detail
- Ability to work with multiple project activities
- Willingness to learn clinical research processes
Key Responsibilities
As a Junior Clinical Research Associate / Clinical Trial Assistant, responsibilities include:
- Develop site and investigator databases for feasibility assessments
- Collect and organize regulatory documents for study start-up
- Coordinate Ethics Committee and DCGI submissions
- Track study start-up activities and timelines
- Maintain Trial Master File (TMF) documentation
- Support internal and external audits
- Assist the Project Manager with site agreements
- Support clinical supplies-related activities
- Assist with project reporting
- Maintain accurate study documentation and trackers
Clinical Research Exposure
Working in this role can provide practical exposure to several areas of clinical research, including:
- Clinical trial start-up
- Site feasibility
- Investigator management
- Regulatory submissions
- Ethics Committee coordination
- DCGI documentation
- Trial Master File management
- Clinical supplies
- Audit support
- Project coordination
This makes the position relevant for graduates planning to build careers in Clinical Research, Clinical Operations, Clinical Trial Management or related functions.
Benefits & Career Development
The supplied job information highlights opportunities such as:
- Exposure to global clinical research operations
- Learning opportunities in clinical trial processes
- Experience with regulatory documentation
- Exposure to international clinical research standards
- Work across therapeutic areas such as Oncology and Rare Disease
- Professional development opportunities
- Collaborative and quality-focused work environment
Job Location
Ahmedabad, Gujarat, India
Work Mode
Office-based | On-site | Full-time
Candidates should be comfortable working from the Ahmedabad office.
How to Apply
Interested candidates can apply through the official REV Clinical careers page.
Position: Junior Clinical Research Associate / Clinical Trial Assistant
Official application:
REV Clinical – Junior CRA / CTA Job Posting
Candidates should select the Apply Now option and submit an updated resume.
Resume Tip
Candidates can highlight relevant:
- Clinical research coursework
- Internship experience
- CRC experience
- Regulatory knowledge
- Clinical trial projects
- Documentation skills
No Walk-In Interview
This is an online application opportunity. No walk-in interview has been announced for this position.
Candidates should apply through the official REV Clinical job posting and check the listing for the latest recruitment status.
Frequently Asked Questions
1. What is the position at REV Clinical?
REV Clinical is hiring for a Junior Clinical Research Associate / Clinical Trial Assistant position in Ahmedabad.
2. Who can apply?
Candidates with M.Pharm, Pharm.D or Life Sciences qualifications can apply.
3. Can freshers apply?
Yes. The listed experience requirement is 0–1 years, making the position suitable for freshers and early-career candidates.
4. Is CRC experience mandatory?
No. CRC experience is preferred, but the role is open to candidates with 0–1 years of experience.
5. Where is the job located?
The position is based in Ahmedabad, Gujarat.
6. Is this a work-from-home job?
No. The role is described as office-based/on-site and full-time.
7. What regulatory experience is useful?
Familiarity with Ethics Committee and DCGI submissions, regulatory documentation and clinical trial start-up processes is useful.
8. Is this a walk-in interview?
No. Candidates need to apply online through the official REV Clinical careers page.
