Clinical Research Coordinators Hiring at Prabhans Clinical Services Kanpur

Clinical Research Coordinators Hiring at Prabhans Clinical Services Kanpur

Clinical Research Coordinators Hiring at Prabhans Clinical Services Kanpur | Oncology & Cardiology Experience Preferred

Prabhans Clinical Services in Kanpur is actively hiring Clinical Research Coordinators and Senior Clinical Research Coordinators for multiple vacancies.


Open Positions

Prabhans Clinical Services is hiring for the following roles:

1. Clinical Research Coordinator (2 Vacancies)

  • Location: Kanpur, Uttar Pradesh
  • Experience: Minimum 1-2 years in clinical research, preferably in Oncology or Cardiology.
  • Salary: ₹12,000 – ₹18,000 per month (based on experience)

This role requires candidates to assist in managing clinical trials, ensuring compliance with regulatory guidelines, and working directly with patients and study teams. Those with prior experience in Oncology or Cardiology will be given preference.

Clinical Research Coordinators Hiring at Prabhans Clinical Services Kanpur
Clinical Research Coordinators Hiring at Prabhans Clinical Services Kanpur

2. Senior Clinical Research Coordinator (2 Vacancies)

  • Location: Kanpur, Uttar Pradesh
  • Experience: Minimum 3-5 years in clinical research with a specialization in Cardiology or Oncology.
  • Salary: ₹18,000 – ₹25,000 per month (based on experience)

Senior Clinical Research Coordinators will oversee trial management and coordinate with multiple stakeholders, including sponsors and investigators. The ideal candidate will have robust experience in clinical documentation, patient monitoring, and regulatory submissions.


Key Responsibilities

For both positions, responsibilities include:

  • Coordinating clinical trial activities in accordance with Good Clinical Practice (GCP) and ICH guidelines.
  • Collecting, documenting, and maintaining clinical trial data.
  • Ensuring timely enrollment of patients and adherence to trial protocols.
  • Assisting in the preparation of clinical study reports.
  • Managing communications between sponsors, study teams, and regulatory bodies.
  • Monitoring patient safety and ensuring compliance with ethical standards.

Senior Clinical Research Coordinators will also lead project management tasks, mentor junior coordinators, and oversee study timelines and budgets.


How to Apply

Interested candidates can apply by sending their updated CVs to:

Upload your CV/resume or any other relevant file. Max. file size: 3 GB.


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