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Fortis Healthcare Hiring For Freshers In Clinical Research Coordinator

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Are you passionate about clinical research and looking to kickstart your career in the healthcare industry? Fortis Healthcare, one of India’s leading integrated healthcare service providers, is hiring for the role of Clinical Research Coordinator in Mumbai. This is an excellent opportunity for candidates with 0-2 years of experience in clinical research to join a reputed organization and contribute to groundbreaking medical studies.

Fortis Healthcare Hiring For Freshers In Clinical Research Coordinator

Job Details

  • Job Title: Clinical Research Coordinator
  • Company: Fortis Healthcare
  • Location: Mumbai
  • Experience: 0-2 Years
  • Salary: 3-4 Lacs P.A.

Educational Qualifications

To be eligible for this role, candidates must have:

  • Bachelor’s degree in Lifesciences, Medical, Biotech, or Public Health.
  • Certification in Clinical Research and basic knowledge of Good Clinical Practice (GCP).

Key Responsibilities

As a Clinical Research Coordinator at Fortis Healthcare, you will play a crucial role in ensuring the smooth execution of clinical trials. Your responsibilities will include:

  1. Coordination: Work closely with the Principal Investigator (PI), Contract Research Organizations (CROs), Sponsors, and Fortis central administration to ensure compliance with protocol, DCGI Schedule Y, and FDA policies.
  2. Study Execution: Assist the PI in patient scheduling, research plan execution, and adherence to protocol requirements.
  3. Documentation: Maintain essential study-related documents, including Trial Master Files (TMF), patient source files, and eCRF filling.
  4. Patient Care: Use clinical skills and empathy to assist study patients with procedures, ensuring their comfort and well-being.
  5. Relationship Building: Establish trust with study participants, offering the highest level of care and monitoring.
  6. Communication: Regularly follow up with participants via phone calls to check on their well-being and remind them of upcoming appointments.
  7. Reporting: Handle SAE (Serious Adverse Event) reporting and other regulatory requirements.
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Key Skills Required

  • Clinical Research
  • Clinical Data Management
  • Clinical Trials
  • Knowledge of GCP and DCGI guidelines
  • Strong communication and interpersonal skills