Clinical Trial Assistant Jobs for Freshers at Bio-Prospera Clinical Research Vasai offering entry-level CRO career growth and learning opportunities in India.
Introduction
Bio-Prospera Clinical Research Pvt. Ltd. is currently inviting applications for the role of Clinical Trial Assistant (CTA) at its Vasai location. This opportunity is designed for freshers and candidates with up to two years of experience who are looking to enter the clinical research and CRO industry. It offers practical exposure to clinical trials, documentation processes, and regulatory standards, making it an excellent starting point for a career in clinical operations.
Company Overview
Bio-Prospera Clinical Research Pvt. Ltd. is an emerging Clinical Research Organization (CRO) focused on conducting bioavailability and bioequivalence (BA/BE) studies along with clinical trials. The company operates with a strong emphasis on compliance, data integrity, and adherence to international regulatory guidelines. With a growing portfolio of clinical projects, Bio-Prospera provides a professional environment for learning and career development in clinical research.
Job Overview
| Job Title | Clinical Trial Assistant (CTA) |
|---|---|
| Company Name | Bio-Prospera Clinical Research Pvt. Ltd. |
| Location | Vasai, Maharashtra |
| Employment Type | Full-Time |
| Qualification | B.Pharm / M.Pharm / B.Sc / M.Sc |
| Experience | 0–2 Years |
| Salary | As per company norms |
| Application Mode |
Job Location & Employment Type
The role is based in Vasai, Maharashtra, and is a full-time, on-site position. Candidates will work closely with clinical research teams, including project managers and clinical research associates, to support trial activities and documentation.
Open Positions / Department Details
The company is hiring for the following role:
- Clinical Trial Assistant (CTA) under Clinical Operations
This role is crucial in ensuring the smooth execution of clinical trials through proper documentation and coordination.
Key Roles & Responsibilities
- Assist Clinical Research Associates (CRAs) and Project Managers in coordinating clinical trial activities
- Prepare and organize documentation for Ethics Committee submissions
- Maintain and update Trial Master File (TMF) and study-related documents
- Coordinate with clinical trial sites for documentation and compliance requirements
- Support site visits including Site Initiation Visits (SIV), monitoring visits, and close-out visits
- Manage logistics related to clinical trials such as investigational products, lab kits, and supplies
- Maintain trackers, logs, and reports for trial progress
- Record meeting minutes and ensure proper communication between stakeholders
- Ensure compliance with ICH-GCP guidelines and regulatory requirements
Eligibility Criteria
Education:
- B.Pharm
- M.Pharm
- B.Sc (Life Sciences, Microbiology, Biotechnology)
- M.Sc (Relevant disciplines)
Experience:
- Freshers are eligible
- Candidates with up to 2 years of experience in clinical research or CRO can apply
Skills Required:
Technical Skills:
- Basic understanding of clinical trial processes
- Knowledge of ICH-GCP guidelines and BA/BE studies
- Familiarity with TMF management and documentation practices
- Proficiency in MS Office tools such as Excel, Word, and Outlook
Soft Skills:
- Strong organizational and documentation skills
- Attention to detail
- Effective communication skills
- Ability to work in a fast-paced and team-oriented environment
- Time management and multitasking ability
Salary & Benefits
- Salary: As per company norms
- Hands-on exposure to clinical trials and regulatory workflows
- Opportunity to work with experienced professionals in the CRO industry
- Learning environment focused on clinical documentation and compliance
- Career growth in clinical operations and research
Selection Process
The recruitment process may include:
- Resume screening
- Technical or functional interview
- HR discussion
- Final selection and onboarding
Candidates should be prepared to demonstrate their understanding of clinical research basics and communication skills.
How to Apply
Interested candidates can apply by sending their updated CV to the official email address:
Ensure your resume highlights your academic background, relevant knowledge, and any internship or project experience related to clinical research.
Why Apply for This Pharma Job?
This Clinical Trial Assistant position is a strong entry point into the clinical research industry. It provides practical exposure to clinical trial management, regulatory documentation, and coordination with clinical sites. Candidates will gain valuable knowledge of GCP guidelines and industry practices, which are essential for long-term career growth in CROs and pharmaceutical companies.
Working at Bio-Prospera allows freshers to build a solid foundation in clinical operations while learning from experienced professionals. This experience can open doors to advanced roles such as Clinical Research Associate (CRA) and Project Coordinator in the future.
Important Note / Disclaimer
PharmaJobHub.in is an independent job information platform. We do not provide any recruitment guarantee and are not affiliated with any company. Candidates are advised to verify details from official sources before applying.
Final Call-to-Action
If you are interested in starting your career in clinical research and meet the eligibility criteria, do not miss this opportunity. Apply early to increase your chances of getting shortlisted.
