Are you a B.Pharm, M.Pharm, MSc, or Clinical Research diploma holder ready to enter the world of clinical trials and regulatory science? This is your golden chance.
Cliniexperts, a reputed Clinical Research Organization (CRO) based in Dwarka Sector 12, New Delhi, is inviting fresh graduates to join their Clinical Operations Team as a Clinical Trial Assistant Intern. Whether you’re looking to gain hands-on experience or begin your pharma industry career, this internship offers the right launchpad.
👨⚕️ What is a Clinical Trial Assistant (CTA)?
A Clinical Trial Assistant (CTA) is an entry-level role that supports the clinical research team in running regulated drug and device trials. You’ll be trained to handle regulatory documentation, patient coordination, data accuracy, and communication with sites, sponsors, and ethical committees.
This internship will expose you to real-world clinical practices and help build a foundation in Good Clinical Practices (GCP), TMF management, and protocol compliance.
🧪 Internship Highlights
- Organization: Cliniexperts
- Position: Clinical Trial Assistant (CTA) Intern
- Type: Internship (Full-time, On-site)
- Location: Dwarka Sector 12, New Delhi
- Eligibility: Freshers (No prior work experience required)
- Preferred Background: B.Pharm, M.Pharm, MSc, or Diploma in Clinical Research
🎯 Key Responsibilities
As a CTA intern, you’ll be part of clinical trial operations that involve:
1. 📄 Clinical Trial Documentation
Assist in preparing, maintaining, and reviewing regulatory documents, site files, and other trial-related materials required by sponsors and regulatory bodies.
2. 🔍 Regulatory Submissions
Help coordinate the timely submission of documents to ethics committees and regulatory authorities under supervision.
3. 🗂️ TMF Maintenance
Support in organizing and maintaining Trial Master Files (TMF) to ensure compliance with audit and inspection standards.
4. 🧑🔬 Site Coordination
Communicate with clinical investigators and site staff to ensure trial processes and documents are up to date.
5. 🧍♀️ Patient Recruitment Support
Provide assistance during volunteer screening, recruitment, and follow-up as per study protocols.
6. 📈 Data Collection & Monitoring
Involved in collecting source data, tracking documents, and assisting during monitoring visits by CRAs (Clinical Research Associates).
✅ Why Choose This Internship?
✨ Career Building Opportunity
Get direct exposure to the CRO environment, learn trial phases, and build your regulatory and documentation skills.
🧘♀️ Work-Life Balance
The internship follows a 5-day work week, promoting both learning and work-life harmony.
📄 Real-Time Documentation Experience
You will learn how to handle regulatory submissions, patient records, and maintain protocol-based documentation – essential skills in clinical research and pharmacovigilance.
👥 Work with Experts
Cliniexperts’ Clinical Operations Team includes seasoned clinical research professionals ready to mentor and train you in industry-relevant best practices.
📌 Internship Requirements
To be eligible, you should meet the following criteria:
- Qualification:
- B.Pharm / M.Pharm
- MSc in Life Sciences
- Diploma in Clinical Research
- Location Availability:
- Must be able to work on-site in Dwarka, New Delhi (Sector 12)
- Core Skills Required:
- Basic knowledge of clinical trials
- Familiarity with GCP guidelines
- Good written and verbal communication
- Attention to detail and professional conduct
🧬 About Cliniexperts
Cliniexperts is a trusted name in Clinical Research Services. From trial management to pharmacovigilance and regulatory compliance, they provide end-to-end solutions to major pharmaceutical and biotech clients. Their New Delhi operations hub is known for its collaborative culture and focus on training the next generation of research professionals.
🧑🎓 Who Should Apply?
This internship is ideal for:
- Fresh graduates looking to enter the pharma/clinical domain
- Pharmacy students interested in transitioning to clinical research
- Individuals wanting a stepping stone into regulatory affairs or medical writing
- Those preparing for full-time CRA or Clinical Project Coordinator roles
📬 How to Apply
Application Process:
- Prepare an updated resume/CV highlighting academic achievements, research skills, and interest in clinical trials.
- Email your CV to: contact@cliniexperts.com
- Use this subject line: “Application for CTA Intern – [Your Name]”
There is no application fee or written test for selection. Shortlisted candidates will be called for an interview or introductory session.
💼 Real Benefits of Doing a CTA Internship
| Benefit | What You Gain |
|---|---|
| 👨⚕️ Industry Exposure | Work with an active clinical trial team in a CRO |
| 📚 Skill Development | Master TMF, GCP, ICH guidelines, and patient data handling |
| 🎓 Resume Boost | Stand out for future CRA or Clinical Data Analyst roles |
| 💼 Career Options | Transition into pharmacovigilance, medical affairs, or QA roles |
✨ Final Thoughts
Clinical research is one of the fastest-growing fields in healthcare, and internships like this one with Cliniexperts can shape your long-term career in pharma and biotech.
If you’re a curious, detail-oriented, and ambitious life science graduate, this CTA internship in New Delhi might be the turning point that sets you apart.
Don’t wait—step into the world of clinical trials and make your mark.
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