Clinical Trial Assistant Job at HRAPL for experienced candidates. Apply via email with 2–3 years CTA experience.
Introduction
A promising opportunity is available for clinical research professionals looking to grow in documentation, site coordination, and trial support roles. This Clinical Trial Assistant (CTA) position is ideal for candidates with prior experience in clinical operations who want to strengthen their expertise in Trial Master File (TMF) management and regulatory compliance. If you are aiming for career growth in clinical research, this role offers a solid pathway.
Company Overview
HRAPL is a growing clinical research organization focused on delivering high-quality clinical trial support and compliance-driven services. The company works on regulated clinical studies and provides professionals with exposure to industry standards such as ICH-GCP and global documentation practices.
Job Location & Employment Type
- Location: Nagpur, Maharashtra, India
- Employment Type: Full-Time
- Work Setup: Office-based Clinical Operations Role
Open Positions / Department Details
- Position: Clinical Trial Assistant (CTA)
- Department: Clinical Operations / Trial Support
- Open Positions: 1
Job Overview (Quick Details Table)
| Category | Details |
|---|---|
| Job Role | Clinical Trial Assistant (CTA) |
| Company | HRAPL |
| Location | Nagpur |
| Qualification | B.Pharm / M.Pharm / BSc / MSc / Biotechnology |
| Experience | 2–3 Years |
| Job Type | Full-Time |
| Industry | Clinical Research |
| Application Mode | |
| Salary Range | ₹3.0 – ₹5.5 LPA |
Key Roles & Responsibilities
As a Clinical Trial Assistant, you will support clinical teams in managing documentation, compliance, and coordination of trial activities.
- Assist in maintaining clinical trial documentation and regulatory records
- Manage and update Trial Master File (TMF/eTMF)
- Support site coordination and communication with stakeholders
- Ensure adherence to ICH-GCP guidelines and internal SOPs
- Track study progress, timelines, and documentation status
- Perform data tracking and quality checks on trial-related documents
- Collaborate with clinical teams to ensure smooth execution of studies
- Assist in audit readiness and compliance activities
Eligibility Criteria
Education
- Bachelor’s or Master’s Degree in:
- Life Sciences
- Pharmacy (B.Pharm / M.Pharm)
- Biotechnology or related field
Experience
- Minimum 2–3 years of experience as a Clinical Trial Assistant (CTA)
- Experience in clinical research and documentation handling is required
Skills Required
- Strong knowledge of clinical trial processes
- Understanding of ICH-GCP guidelines
- Experience with TMF/eTMF management
- Proficiency in MS Excel and documentation tools
- Good organizational and communication skills
- Ability to manage site coordination and data tracking efficiently
Salary & Benefits
- Salary: ₹3.0 – ₹5.5 LPA (estimated)
- Exposure to regulated clinical trials and documentation systems
- Opportunity to work on TMF, site coordination, and compliance processes
- Career growth in clinical operations and research
- Hands-on experience in audit preparation and regulatory standards
Selection Process
The hiring process may include:
- Email application submission
- Resume shortlisting
- Technical interview
- HR discussion
- Final selection
How to Apply
- Interested candidates should apply via email
- Send your updated CV to: contact@hrapl.in
- Subject Line: Name_CTA
- Ensure your resume highlights:
- CTA experience
- TMF handling
- GCP knowledge
- Clinical trial exposure
Important Dates
- Last Date to Apply: Not specified (Apply as soon as possible)
Why Apply for This Pharma Job?
This role is an excellent opportunity for professionals who want to strengthen their foundation in clinical research operations. It provides hands-on exposure to TMF management, regulatory documentation, and site coordination—key areas in clinical trials. Candidates will gain valuable experience in compliance and audit readiness, which are essential for career advancement in clinical research. Additionally, this position offers stable growth and learning opportunities within a developing clinical research organization.
Important Note / Disclaimer
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Final Call-to-Action
Eligible candidates with relevant CTA experience should apply immediately via email to secure this opportunity in clinical research operations.
