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Gandhinagar – Eccentric Clinical Research is looking for enthusiastic and detail-oriented individuals to join our team. We have an immediate opening for a Clinical Trial Assistant (CTA) Intern at our Gandhinagar location.
This is a fantastic opportunity for recent graduates and early-career professionals. If you have a passion for life sciences and clinical research, we encourage you to apply. Join us to build a strong foundation for your career in a dynamic environment.
Open Position: CTA Intern
Location: Gandhinagar, Gujarat
Job Description
As a CTA Intern, you will be integral to our clinical trial operations. You will provide essential support to our project teams and gain invaluable hands-on experience. Your key responsibilities will include:
- Assisting in the preparation, maintenance, and updating of the Trial Master File (TMF/eTMF).
- Supporting the preparation, submission, and tracking of regulatory and ethics committee documents.
- Ensuring proper filing, version control, and archival of essential study documents.
- Assisting Project Managers and CRAs with study setup, feasibility, initiation, monitoring, and close-out activities.
- Tracking project progress through dashboards, trackers, and reports to ensure timelines are met.
- Supporting site payments, investigator communications, and vendor coordination.
- Managing the shipment, distribution, and tracking of study supplies.
- Assisting in maintaining investigator and vendor databases.
- Ensuring trial activities comply with SOPs, ICH-GCP, and local regulations.
- Supporting preparations for audits, inspections, and CAPA documentation.
- Assisting in safety reporting documentation and SAE tracking.
- Contributing to departmental initiatives and process improvements.
- Gaining practical experience to progress into future CRA roles.
Qualifications and Required Skills
We are looking for candidates who meet the following criteria:
- Education: Bachelor’s degree in Life Sciences, B.Pharm, or M.Pharm.
- Experience: 0-2 years in clinical research. Fresh graduates with a strong academic background or relevant internships are welcome to apply.
- Knowledge: A strong understanding of clinical trial processes, GCP, and regulatory requirements is an advantage.
- Organizational Skills: Excellent documentation, organizational, and communication abilities.
- Technical Proficiency: Proficient in MS Office (Word, Excel, PowerPoint) and comfortable working with clinical trial software.
- Work Ethic: Ability to multitask, prioritize, and thrive in a fast-paced team environment.
How to Apply
Ready to launch your career in clinical research? We want to hear from you!
SEND YOUR CV TO: hr@eccentriccr.com
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For More Information
To learn more about our company and what we do, please visit our website: www.eccentriccr.com