Clinical Trial Assistant

Published on

HREE Research Pvt. Ltd.

Default Logo
🎓 Pharma
📍 Ahmedabad & Pune
💼 0 - 1 years
Verified Job
Email Application
💬

Join Our WhatsApp Group

Get daily alerts of new job openings & internships directly on your phone!

Join Group
HREE Research is seeking enthusiastic Clinical Trial Assistants to support clinical operations across Ahmedabad and Pune. The role involves assisting with clinical trial coordination, documentation, regulatory compliance, and site management activities. Candidates will gain valuable exposure to clinical operations while working with experienced professionals in a quality-focused CRO environment. This opportunity provides an excellent platform to build a successful career in pharmaceutical clinical research.

Job Overview

Particulars Details
Position Clinical Trial Assistant
Company HREE Research Pvt. Ltd.
Location Ahmedabad & Pune
Job Type Full-Time
Experience 0 - 1 years
Category / Department Pharma
Application Mode Email

🏢 About HREE Research Pvt. Ltd.

Company Overview

HREE Research Pvt. Ltd. is a full-service Clinical Research Organization (CRO) providing high-quality clinical research solutions to pharmaceutical and biotechnology companies across multiple therapeutic areas.

Company Mission

To deliver reliable, compliant, and innovative clinical research services that accelerate the development of safe and effective medicines.

Company Vision

To become a trusted global clinical research partner through quality, innovation, and patient-centered research excellence.

Core Values

• Integrity
• Innovation
• Quality
• Compliance
• Patient Focus
• Collaboration
• Continuous Improvement

What Makes Them Different

HREE combines scientific expertise, regulatory excellence, and operational efficiency to deliver high-quality clinical research services while supporting employee development and career growth.

Leadership/Company Philosophy

The organization believes in ethical research practices, continuous learning, teamwork, and delivering value to clients while improving healthcare outcomes worldwide.

🌐
Company Website
📍
Office Location

HREE Research Pvt. Ltd.
Ahmedabad, Gujarat, India
Pune, Maharashtra, India

Clinical Trial Assistant Banner

💡 Editor's Note / Preparation Tip

📄 Resume Preparation Tips

• Highlight your Clinical Research Coordinator (CRC) experience.
• Mention GCP knowledge and clinical trial documentation.
• Include any Diploma in Clinical Research or relevant certifications.
• Showcase communication, coordination, and organizational skills.
• Optimize your resume with clinical research keywords for ATS.

🎯 Interview Preparation

• Revise clinical trial phases and GCP guidelines.
• Understand the responsibilities of a Clinical Trial Assistant.
• Prepare examples of documentation and site coordination activities.
• Review regulatory and ethics committee submission basics.
• Demonstrate strong communication and teamwork skills.

💡 Professional Tips

• Stay updated with ICH-GCP and clinical research regulations.
• Improve documentation and data management skills.
• Build expertise in clinical trial coordination processes.
• Learn clinical research software and digital tools.
• Focus on accuracy, compliance, and patient safety throughout your career.

📝 Job Description

🚀 Clinical Trial Assistant Hiring | HREE Research Pvt. Ltd. | Ahmedabad & Pune

Looking to build your career in Clinical Research? HREE Research Pvt. Ltd., a growing Clinical Research Organization (CRO), is hiring Clinical Trial Assistants for its Ahmedabad and Pune locations. This opportunity is ideal for candidates with a B.Pharm or Life Sciences background and 3–4 months of Clinical Research Coordinator (CRC) experience who want to grow in pharmaceutical clinical research. Join a dynamic organization dedicated to innovation, regulatory excellence, and patient-focused clinical trials.


📌 Position Details

💼 Position: Clinical Trial Assistant (CTA)
🏢 Company: HREE Research Pvt. Ltd. (HRE)
📍 Location: Ahmedabad & Pune
🏢 Work Mode: On-site
💼 Experience: 3–4 Months as Clinical Research Coordinator (CRC)
🎓 Qualification: B.Pharm or Life Sciences (Diploma in Clinical Research Preferred)
📄 Employment Type: Full-Time
Joining Preference: Immediate / As Per Company Requirement


⭐ Preferred Skills

⭐ Diploma in Clinical Research
⭐ Experience as a Clinical Research Coordinator (CRC)
⭐ Knowledge of regulatory guidelines and ethics submissions
⭐ Strong documentation practices
⭐ Ability to manage multiple study activities
⭐ Problem-solving and analytical thinking
⭐ Adaptability in a fast-paced clinical research environment


🎓 Candidate Requirements

• B.Pharm or Life Sciences background.
• 3–4 months of Clinical Research Coordinator (CRC) experience.
• Diploma in Clinical Research is preferred.
• Basic understanding of clinical trial processes and Good Clinical Practice (GCP).
• Strong organizational and documentation skills.
• Good verbal and written communication abilities.
• Ability to work collaboratively in a clinical research environment.


🌟 Why Join HREE Research Pvt. Ltd.?

✔ Build your career with a growing Clinical Research Organization (CRO).
✔ Gain practical experience in clinical operations and trial management.
✔ Exposure to diverse therapeutic areas and pharmaceutical research projects.
✔ Supportive and collaborative work culture.
✔ Continuous learning and professional development opportunities.
✔ Long-term career growth in the clinical research industry.
✔ Contribute to ethical and patient-focused clinical research.


📩 How to Apply

Apply through the JobPortalConnect application page:

📧 hr@hree.org

Email Subject: HREE_CTA_Ahmedabad or HREE_CTA_Pune

🌐 Company Website: https://hree.org/

📢 Know someone who would be a great fit? Tag them or share this opportunity with your network!

🎯 Key Responsibilities

  • Assist in coordinating clinical trial activities across study sites.
  • Support clinical documentation and maintain accurate trial records.
  • Assist site management and monitoring activities.
  • Ensure data accuracy and timely documentation.
  • Support regulatory and ethics committee submissions.
  • Coordinate with cross-functional teams involved in clinical studies.
  • Ensure compliance with study protocols, GCP guidelines, and regulatory requirements.
  • Contribute to smooth execution of clinical research projects.

💡 Required Qualifications & Skills

Clinical Trial Coordination Clinical Research Documentation Good Clinical Practice (GCP) Knowledge Site Management Support Clinical Data Accuracy Regulatory & Ethics Documentation Trial Record Maintenance Organizational Skills Communication Skills Team Collaboration Attention to Detail Time Management Understanding of Clinical Trial Processes
Contact Email: hr@hree.org

Frequently Asked Questions

Q1. Who is eligible to apply?
✅ Candidates with a B.Pharm or Life Sciences background and 3–4 months of CRC experience.

Q2. Is a Diploma in Clinical Research mandatory?
✅ No, it is preferred but not mandatory.

Q3. Which locations are available?
✅ Ahmedabad and Pune.

Q4. How do I apply?
✅ Send your resume with the subject line HREE_CTA_Ahmedabad or HREE_CTA_Pune based on your preferred location.

Q5. Is this suitable for freshers?
✅ Candidates with 3–4 months of CRC experience are preferred. Freshers with relevant qualifications may also be considered.

🛡️ Safety Disclaimer: JobPortalConnect curates official listings for informational purposes. Genuine recruiters will never ask you for processing fees, training payments, or security deposits. If you spot suspicious activity, copyright issues, or wish to request the removal of this listing, please report it to us immediately at contact.jobportalconnect@gmail.com.