Looking to build a rewarding career in clinical research? Here’s an exciting opportunity for professionals with Clinical Research Coordinator (CRC) experience. HREE Research Private Limited has announced 04 openings for the position of Clinical Trial Assistant (CTA) across Pune and Ahmedabad.

If you have recently worked as a CRC and want to transition into a corporate clinical operations role, this recruitment drive can be your next career milestone. The CTA role provides excellent exposure to Trial Master File management, regulatory documentation, sponsor communication, and clinical project coordination.

Let’s explore everything you need to know before applying.

🏢 About HREE Research Private Limited

HREE Research Private Limited is a growing Clinical Research Organization (CRO) providing high-quality clinical research support services for pharmaceutical, biotechnology, and healthcare companies. The organization works with clinical investigators, hospitals, ethics committees, and sponsors to ensure that clinical studies are conducted according to international quality standards and regulatory guidelines.

Working with a CRO like HREE Research helps professionals gain valuable exposure to real-world clinical trial operations, making it an ideal workplace for those planning long-term careers in clinical research.

📋 HREE Research CTA Recruitment 2026 – Job Details

Particular	Details
Company	HREE Research Private Limited
Job Role	Clinical Trial Assistant (CTA)
Locations	Pune & Ahmedabad
Number of Vacancies	04
Qualification	B.Pharm / Life Sciences Graduate or Postgraduate
Preferred Qualification	PG Diploma in Clinical Research (PGDCR)
Experience	3–4 months as Clinical Research Coordinator (CRC)
Job Type	Full-Time
Department	Clinical Operations

🌟 What Does a Clinical Trial Assistant (CTA) Do?

The Clinical Trial Assistant is an important member of every clinical operations team. While Clinical Research Associates monitor studies at different sites, CTAs provide administrative and operational support that keeps clinical trials organized and compliant.

This role involves handling essential clinical documents, maintaining project trackers, coordinating with investigators, and ensuring smooth communication between sponsors and study sites.

For professionals planning to become a Clinical Research Associate (CRA), Clinical Project Coordinator, or Clinical Project Manager, working as a CTA provides an excellent learning opportunity.

📌 Key Responsibilities

Selected candidates will be responsible for:

📁 Managing Trial Master File (TMF) and Electronic Trial Master File (eTMF)
📄 Filing and maintaining essential clinical trial documents
📝 Supporting regulatory documentation and ethics committee submissions
📊 Maintaining project trackers and study logs
📦 Coordinating shipment of study materials and laboratory kits
📧 Communicating with investigators, hospitals, sponsors, and project teams
📅 Scheduling meetings and preparing Minutes of Meetings (MoMs)
📂 Supporting document archiving according to SOPs
✔ Ensuring documents remain inspection and audit ready
📈 Assisting Clinical Trial Managers with daily project activities

🎓 Eligibility Criteria

Candidates should possess:

Bachelor’s degree in Pharmacy (B.Pharm)
OR Graduate/Postgraduate degree in Life Sciences
Biotechnology
Microbiology
Biochemistry
Genetics
Zoology
Biomedical Sciences
Other related Life Science disciplines

Preferred Qualification

Candidates holding a PG Diploma in Clinical Research (PGDCR) will have an added advantage during screening.

💼 Experience Required

Applicants should have:

3–4 months of experience as a Clinical Research Coordinator (CRC)
Basic understanding of Good Clinical Practice (GCP)
Knowledge of essential clinical trial documentation
Experience handling investigator site documents
Familiarity with Microsoft Excel, Word, and PowerPoint

📚 Skills Required

Successful candidates should possess:

Excellent communication skills
Good documentation practices
Strong organizational ability
Attention to detail
Time management
Team collaboration
Knowledge of clinical trial workflow
Ability to maintain confidential documents
Basic regulatory understanding

🚀 Career Growth After Joining

Working as a Clinical Trial Assistant opens several career opportunities, including:

Clinical Research Associate (CRA)
Senior CTA
Clinical Trial Coordinator
Project Coordinator
Clinical Operations Executive
Clinical Project Manager
TMF Specialist
Regulatory Affairs Associate

Many professionals begin as CTAs before moving into monitoring and project management roles within global CROs.

🌍 Why Join HREE Research?

Some advantages of working with HREE Research include:

✅ Exposure to real clinical trial projects

✅ Opportunity to work with experienced clinical professionals

✅ Learning global documentation standards

✅ Professional work environment

✅ Career progression within clinical operations

✅ Experience with multinational sponsors

✅ Strong foundation for future CRA opportunities

📧 How to Apply?

Interested candidates should prepare an updated resume highlighting their CRC experience and educational qualifications.

Send your CV to:

📩 hr@hree.org

Email Subject Line

Ahmedabad Position

HREE_CTA_Ahmedabad

Pune Position

HREE_CTA_Pune

Applying for Both

HREE_CTA_Ahmedabad and Pune

Apply as early as possible since screening interviews are expected to begin soon.

💡 Tips to Increase Your Selection Chances

Before submitting your application:

Update your latest resume
Mention your exact CRC experience
Include GCP certification if available
Highlight TMF or eTMF experience
Mention internship projects
Add Microsoft Office proficiency
Proofread your resume before sending

A well-structured resume significantly improves your chances of getting shortlisted.

📌 Who Should Apply?

This opportunity is ideal for:

B.Pharm graduates
M.Pharm graduates with CRC experience
Life Science graduates
Biotechnology graduates
Microbiology graduates
Biochemistry graduates
Genetics graduates
Clinical Research professionals
PGDCR candidates
Clinical Research Coordinators looking for career advancement

📢 Final Thoughts

The HREE Research Clinical Trial Assistant Recruitment 2026 offers an excellent opportunity for aspiring clinical research professionals who already possess initial CRC experience. The role provides practical exposure to clinical operations, documentation management, regulatory compliance, and project coordination—all essential skills for building a successful career in the pharmaceutical and CRO industry.

If you meet the eligibility criteria, don’t delay your application. Early applicants often have a better chance of being shortlisted.

Good luck with your clinical research journey!

❓Frequently Asked Questions (FAQs)

1. Who can apply for the HREE Research CTA position?

Candidates with a B.Pharm or Life Sciences degree and 3–4 months of CRC experience can apply.

2. Is PGDCR mandatory?

No. It is preferred but not mandatory.

3. Where are the job locations?

The openings are available in Pune and Ahmedabad.

4. How many vacancies are available?

There are 04 Clinical Trial Assistant vacancies.

5. What is the required experience?

Applicants should have 3–4 months of Clinical Research Coordinator (CRC) experience.

🏷️ Focus Keyword

HREE Research Clinical Trial Assistant Recruitment 2026

HREE Research Clinical Trial Assistant Recruitment 2026 | 04 Openings in Pune & Ahmedabad