The clinical research industry in India continues to expand rapidly, creating exciting career opportunities for Life Sciences, Pharmacy, and Nursing graduates. If you have experience in clinical trials and are looking to build a rewarding career in research, Bio-Prospera Clinical Research Pvt. Ltd. has announced a walk-in recruitment drive for the position of Clinical Trials Assistant (CTA) at its Vasai East facility in Maharashtra.

This opportunity is ideal for candidates who want hands-on exposure to clinical trial documentation, patient coordination, regulatory compliance, and Good Clinical Practice (GCP). Read on for complete details about the eligibility criteria, responsibilities, interview schedule, and preparation tips.

About Bio-Prospera Clinical Research Pvt. Ltd.

Bio-Prospera Clinical Research Pvt. Ltd. is a clinical research organization committed to delivering high-quality clinical trial services while maintaining international standards of ethics, compliance, and patient safety. Guided by its vision of “Innovation for Better Tomorrow,” the company supports pharmaceutical and healthcare organizations through efficient clinical research operations.

Working with Bio-Prospera offers professionals an opportunity to gain practical exposure to clinical trial management, regulatory documentation, and collaborative research projects that contribute to the development of new healthcare solutions.

Bio-Prospera Recruitment 2026 – Overview

Particular	Details
Company	Bio-Prospera Clinical Research Pvt. Ltd.
Position	Clinical Trials Assistant (CTA)
Experience	6 Months to 1 Year
Qualification	B.Sc, M.Sc (Life Sciences), B.Pharm, M.Pharm, Nursing, or related Life Science disciplines
Job Location	Vasai East, Maharashtra
Industry	Clinical Research / Pharmaceuticals
Interview Mode	Walk-In

Eligibility Criteria

Candidates applying for this position should meet the following requirements:

Bachelor’s or Master’s degree in Life Sciences or related disciplines.
B.Pharm, M.Pharm, or Nursing graduates are also eligible.
6 months to 1 year of experience in Clinical Research is preferred.
Basic understanding of ICH-GCP guidelines and clinical trial processes.
Good knowledge of Microsoft Word and Microsoft Excel.
Strong written and verbal communication skills.
Excellent organizational skills with attention to detail.

Roles and Responsibilities

As a Clinical Trials Assistant (CTA), you will support the clinical operations team by ensuring smooth documentation and coordination throughout the study lifecycle.

Your responsibilities include:

Maintaining Trial Master Files (TMF) and Investigator Site Files (ISF).
Assisting with clinical trial documentation and regulatory records.
Supporting patient scheduling and participant coordination.
Collecting and organizing study-related data accurately.
Ensuring compliance with Good Clinical Practice (GCP), study protocols, and Standard Operating Procedures (SOPs).
Coordinating with investigators, Clinical Research Associates (CRAs), and project teams.
Preparing documents for audits and inspections.
Maintaining confidentiality of patient and study information.

Preferred Skills

Bio-Prospera is looking for candidates who possess:

Knowledge of ICH-GCP Guidelines
Clinical documentation skills
Trial Master File (TMF) management
MS Office proficiency
Communication and interpersonal skills
Time management
Problem-solving ability
Accuracy and attention to detail

Expected Salary

The company has not officially disclosed the salary package.

Based on current industry standards, candidates with 6 months to 1 year of experience can expect an annual CTC in the range of:

₹2.8 LPA – ₹4.5 LPA

Actual compensation may vary depending on experience, interview performance, and company policy.

Walk-In Interview Details

Particular	Details
Interview Date	From 15 July 2026 onwards (Monday to Friday)
Interview Time	10:00 AM – 2:00 PM
Venue	Bio-Prospera Clinical Research Pvt. Ltd., Viraj Industrial Estate, Plot No. 44, Dewan & Shah Udyog Nagar, Chinchpada, Vasai East, Maharashtra – 401208
Contact Number	+91 9730151113
Email	hr@bpclinical.com
Website	www.bioprosperaclinical.com

Documents to Carry

Candidates attending the walk-in interview should carry:

Updated Resume
Passport-size photographs
Educational certificates
Experience certificate
Government-issued ID proof
Latest salary slip (if applicable)

How to Apply

Interested and eligible candidates can directly attend the walk-in interview at the venue during the scheduled dates and timings.

Candidates who are unable to attend the walk-in interview may send their updated resume to the HR email address mentioned above, subject to the company’s recruitment process.

Interview Preparation Tips

To improve your chances of selection, revise the following topics before attending the interview:

1. ICH-GCP Guidelines

Understand the principles of Good Clinical Practice, informed consent, patient safety, investigator responsibilities, and documentation standards.

2. Clinical Trial Phases

Know the objectives and differences between Phase I, II, III, and IV clinical trials.

3. Trial Master File (TMF)

Learn the purpose of the Trial Master File, essential documents, and audit readiness.

4. Important Clinical Research Terms

Prepare definitions of:

Protocol
Investigator Brochure (IB)
Informed Consent Form (ICF)
Serious Adverse Event (SAE)
Case Report Form (CRF)
Investigational Product (IP)
Standard Operating Procedure (SOP)

5. Practical Experience

Be prepared to explain your previous clinical research experience using real examples. Highlight how you managed documentation, maintained compliance, coordinated with study teams, and ensured data accuracy.

Career Growth

A Clinical Trials Assistant role provides an excellent foundation for a long-term career in clinical research. With experience and additional certifications, professionals can progress into positions such as:

Clinical Research Coordinator (CRC)
Clinical Research Associate (CRA)
Senior CRA
Clinical Trial Monitor
Clinical Project Coordinator
Clinical Project Manager
Regulatory Affairs Associate
Clinical Operations Manager

The experience gained in this role can also open opportunities with leading pharmaceutical companies, CROs, biotechnology organizations, and healthcare institutions across India and internationally.

Why Consider This Opportunity?

Work with an established Clinical Research Organization.
Gain practical exposure to real-world clinical trials.
Build expertise in GCP and regulatory documentation.
Develop skills valued across the pharmaceutical and healthcare industries.
Excellent opportunity for early-career clinical research professionals.

Disclaimer

The recruitment details shared above are intended solely for informational purposes. We are not a recruitment agency and do not charge any fee for job applications. Candidates are advised to verify all information through the company’s official communication before attending the interview.

Frequently Asked Questions (FAQs)

Who can apply for the Clinical Trials Assistant position?

Candidates with B.Sc, M.Sc (Life Sciences), B.Pharm, M.Pharm, Nursing, or related qualifications and 6 months to 1 year of relevant experience can apply.

Is this opportunity open to freshers?

The company prefers candidates with prior experience ranging from 6 months to 1 year.

Where is the job located?

The position is based in Vasai East, Maharashtra.

Is knowledge of GCP required?

Yes. A basic understanding of ICH-GCP guidelines is one of the preferred qualifications.

What documents should I bring to the interview?

Carry an updated resume, educational certificates, experience certificate, ID proof, passport-size photographs, and salary slip (if applicable).

Bio-Prospera Walk-In Drive 2026: Clinical Trials Assistant (CTA) Jobs in Vasai | Apply Directly