eAspire Technolabs Inc. is hiring for the position of Clinical Trial Assistant in Ahmedabad, Gujarat. Candidates with a Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, Microbiology, Nursing, or related disciplines are eligible to apply.
This is a full-time opportunity for candidates with 0–1 year of experience. Freshers interested in clinical research and clinical trial management are also encouraged to apply.
The selected candidates will support clinical research teams in trial coordination, Trial Master File (TMF) and Investigator Site File (ISF) maintenance, regulatory documentation, and clinical study activities.
Job Details – eAspire Technolabs Recruitment
| Particulars | Details |
|---|---|
| Company | eAspire Technolabs Inc. |
| Recruitment Posted By | Evoke HR |
| Job Role | Clinical Trial Assistant |
| Department | Pharmaceutical & Biotechnology |
| Job Location | Ahmedabad, Gujarat |
| Experience | 0–1 Year |
| Qualification | B.Pharm, M.Pharm, Pharm.D, B.Sc. / M.Sc. in relevant disciplines |
| Job Type | Full-Time |
| Employment Type | Full-Time, Permanent |
| Openings | 1 |
| Industry | IT Services & Consulting |
| Job Category | Pharmaceutical & Biotechnology |
| Role Category | Clinical Research Scientist |
Position Available
Clinical Trial Assistant
The Clinical Trial Assistant will support the planning, coordination, and execution of clinical research studies while maintaining essential trial documentation and ensuring compliance with study protocols and Good Clinical Practice (GCP) standards.
Key Responsibilities
- Assist clinical research teams in coordinating and managing clinical trial activities.
- Prepare, organize, and maintain essential clinical trial documents.
- Support Trial Master File (TMF) and Investigator Site File (ISF) maintenance.
- Assist in preparing clinical trial protocols and informed consent forms.
- Track clinical trial progress, timelines, and study milestones.
- Coordinate with Clinical Research Associates (CRAs), investigators, sponsors, and research teams.
- Support regulatory document collection, review, and submission processes.
- Maintain accurate records of clinical trial activities and study correspondence.
Eligibility Criteria & Educational Qualifications
Candidates with the following educational qualifications can apply:
- B.Pharm – Bachelor of Pharmacy
- M.Pharm – Master of Pharmacy
- Pharm.D – Doctor of Pharmacy
- B.Sc. / M.Sc. in Life Sciences
- B.Sc. / M.Sc. in Biotechnology
- B.Sc. / M.Sc. in Microbiology
- Nursing graduates
- Other related disciplines
Experience: 0–1 year. Freshers interested in clinical research and clinical trial management are encouraged to apply.
Additional Requirements:
- Basic understanding of clinical trials and clinical research processes.
- Knowledge of medical terminology.
- Understanding of clinical trial documentation.
Required Skills
- Clinical Trial Coordination and Administration
- Clinical Research Documentation
- Trial Master File (TMF) Management
- Investigator Site File (ISF) Maintenance
- ICH-GCP Guidelines
- Regulatory Documentation
- Clinical Operations
- Clinical Research
- Life Sciences
