"Complete Success Guide for Pharma & Medical Students (2025-26)"

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"Ultimate Success Guide for Medical & Pharma Students: How to Build a Strong Career and Achieve Your Dreams in 2025-26" (Complete Success Guide for Pharma & Medical Students 2025–26) Success in the medical and pharma field does not depend only on degrees. It requires the right mindset, planning, skills, and long-term consistency. Whether you are a B.Pharm, M.Pharm, Pharm.D, MSc, Nursing, BSc Biology, Biotechnology, Microbiology, or any medical student, this guide will help you move in the right direction and build a career you are proud of. In 2025, the healthcare industry is expanding faster than ever—offering global salaries, international opportunities, and limitless growth for skilled students. If you want to succeed, this article will give you a step-by-step roadmap to shape your future. ★ 1. Build a Strong Foundation in Your Basics:- Every successful medical student starts from one common step: clarity of concepts. A strong foundation in subjects like: Human ana...

"Clinical Trial Assistant (CTA) Internship at Eccentric Clinical Research, Gandhinagar – Apply Now" ✅

"Clinical Trial Assistant (CTA) Interns Jobs at Eccentric Clinical Research – Gandhinagar, Gujarat"


Eccentric Clinical Research, a rapidly growing Contract Research Organization (CRO) in India, is inviting applications for Clinical Trial Assistant (CTA) Interns at its Gandhinagar, Gujarat facility. This is an excellent opportunity for fresh graduates in Life Sciences, B.Pharm, or M.Pharm who are passionate about building a career in clinical trials, GCP compliance, and regulatory affairs.

Working as a CTA Intern at Eccentric Clinical Research will give you practical exposure to clinical operations, documentation, and regulatory submissions, along with mentorship from experienced professionals.


Key Responsibilities – CTA Intern:-

As a Clinical Trial Assistant Intern, you will:

  • Maintain and update the Trial Master File (TMF/eTMF).
  • Assist with regulatory and ethics committee submissions and documentation.
  • Handle version control, filing, and archival of study documents.
  • Support CRAs and Project Managers during study setup, initiation, monitoring, and close-out activities.
  • Track clinical trial progress using dashboards, trackers, and reports.
  • Coordinate with sites, investigators, and vendors for trial-related activities.
  • Manage distribution and tracking of study supplies and shipments.
  • Ensure compliance with ICH-GCP guidelines, SOPs, and regulatory requirements.
  • Contribute to safety reporting, SAE tracking, audit readiness, and process improvements.

Eligibility Criteria:-

  • Qualification: B.Sc / M.Sc (Life Sciences), B.Pharm, or M.Pharm.
  • Experience: 0–2 years (freshers with internships are encouraged).
  • Skills Required:
    • Knowledge of clinical trial processes, ICH-GCP, and regulatory guidelines.
    • Strong organizational & documentation skills.
    • Proficiency in MS Office (Word, Excel, PowerPoint) and trial management tools.
    • Ability to multitask and work in fast-paced environments.

Why Join Eccentric Clinical Research?

✅ Hands-on experience in clinical operations & trial management.
✅ Training & mentorship from senior CRAs and project managers.
✅ Exposure to regulatory submissions and eTMF systems.
✅ Growth opportunities into CRA and Project Management roles.
✅ Supportive and collaborative work culture.


Job Location:-

  • Gandhinagar, Gujarat, India

Salary Package:-

  • INR 2,00,000 – 3,60,000 per annum (depending on qualifications and performance).

How to Apply?

Interested candidates can apply by sending their updated CV to:
📧 hr@eccentriccr.com

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