Looking to start your career in clinical research and clinical trial management? A promising opportunity is now open for the role of Executive โ Clinical Trial Management (NCE) in Ahmedabad, Gujarat. This role is ideal for Pharm.D, M.Pharm, and Life Sciences freshers aiming to enter the clinical research domain.
This Clinical Trial Assistant (CTA) job in Ahmedabad offers exposure to global Phase 1โ4 clinical trials, regulatory processes, and Trial Master File (TMF) managementโmaking it a strong entry point into the pharmaceutical and CRO industry.
๐ Job Overview
- Role: Executive โ Clinical Trial Management (CTA)
- Location: Ahmedabad, Gujarat, India
- Department: Clinical Trial Management (NCE)
- Qualification: Pharm.D / M.Pharm / Life Sciences
- Experience: Freshers can apply
- Job Type: Full-Time
- Application Deadline: 11 May 2026
๐ Key Responsibilities โ Clinical Trial Assistant Role
As a Clinical Trial Assistant (CTA), you will support global clinical operations teams in managing trials efficiently:
- Assist in Phase 1โ4 clinical trials for New Chemical Entities (NCE)
- Maintain and manage Trial Master File (TMF) as per ICH-GCP guidelines
- Track study milestones, patient recruitment, and site activities
- Support protocol amendments, IB updates, and ICF revisions
- Prepare and review clinical documents and study materials
- Assist in regulatory submissions (IND, CTA, EC submissions)
- Coordinate safety reporting documentation (SUSAR, DSUR, PSUR)
- Communicate with CROs, clinical sites, and vendors globally
- Support audit readiness and regulatory inspections
- Maintain clinical trial documentation systems (CTMS, EDC)
๐ Qualifications & Eligibility
Required:
- B.Pharm / Pharm.D (mandatory)
- Basic understanding of clinical trials and regulatory processes
Preferred:
- M.Pharm / Life Sciences / Biotechnology
- Knowledge of:
- ICH-GCP guidelines
- Clinical trial lifecycle
- TMF, CTMS, EDC systems
๐ง Required Skills
Technical Skills:
- Clinical trial documentation & compliance
- Regulatory submissions knowledge
- Pharmacovigilance basics
- Data integrity and documentation
Soft Skills:
- Strong organizational ability
- Attention to detail
- Communication & stakeholder coordination
- Ability to work in global teams
๐ฐ Salary & Benefits
- Estimated Salary: โน3.0 โ โน5.5 LPA (based on market standards for CTA roles)
- Exposure to global clinical trials
- Career growth in clinical research & drug development
- Work with cross-functional international teams
- Learning opportunities in AI/ML applications in clinical trials
๐ Why This Clinical Trial Job Matters
This clinical trial assistant job for freshers provides hands-on experience in:
- Global drug development lifecycle
- Regulatory frameworks (FDA, EMA, CDSCO)
- Clinical documentation and compliance
- Real-world clinical operations
It is a strong foundation for careers in:
- Clinical Research Associate (CRA)
- Clinical Project Management
- Regulatory Affairs
- Pharmacovigilance
๐ฅ How to Apply
