Shivensis Research Hiring for Clinical Research Coordinator

Are you passionate about clinical trials and looking to begin or grow your career in clinical research?
Shivensis Research is hiring Clinical Research Coordinators (CRC) for its Bathinda, Punjab site.
This is an excellent opportunity for Life Sciences, Pharmacy, and Biotechnology graduates to gain hands-on experience in clinical trial operations, GCP compliance, and regulatory documentation.

🧩 Key Responsibilities

As a Clinical Research Coordinator (CRC) at Shivensis Research, you will:

1. Manage and oversee day-to-day operations of clinical trials.
2. Assist Principal Investigators (PI) in participant recruitment and informed consent.
3. Screen and enroll study participants per protocol.
4. Ensure compliance with Good Clinical Practice (GCP), study protocols, and regulatory requirements.
5. Monitor and report Adverse Events (AE) and Serious Adverse Events (SAE).
6. Liaise with CROs, investigators, and Ethics Committees (EC).
7. Support audits, site visits, and inspections.
8. Prepare regular study progress reports and updates for management.

🎓 Qualification & Experience

• Education: Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or Biotechnology.
• Experience:
  • Freshers or candidates with 1–2 years of experience in clinical research or clinical trial coordination are encouraged to apply.
• Position Type: Full-time, on-site (Bathinda, Punjab).

💼 Why Join Shivensis Research?

• Opportunity to work in a growing clinical research organization.
• Hands-on experience in clinical trial management and GCP compliance.
• Exposure to audits and regulatory processes.
• Collaborative work environment with professional development support.

📍 Job Location

Bathinda, Punjab

📨 How to Apply

Interested candidates can submit their resume to:
📧 shivensisresearch@gmail.com