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Shree Clinical Research Services Hiring for Freshers as Clinical Research Coordinator

Job Posting: Clinical Research Coordinator (CRC)

Job Summary:
Shree Clinical Research Services Pvt Ltd is currently seeking a dedicated and detail-oriented Clinical Research Coordinator (CRC) to join our team in Hubli, Karnataka. This role is a fantastic opportunity for both fresh graduates and experienced professionals to build a strong foundation in the clinical research industry. The successful candidate will play a pivotal role in supporting clinical trial operations, managing patient interactions, and ensuring accurate documentation. If you are passionate about life sciences and looking for a hands-on, on-site role in a rapidly growing sector, we invite you to apply.


Job Overview

  • Role: Clinical Research Coordinator (CRC)
  • Location: Hubli, Karnataka (On-site)
  • Experience: Freshers and Experienced candidates are welcome
  • Shift: Day Shift
  • Eligibility: Must be a resident of Karnataka

Responsibilities

As a Clinical Research Coordinator, you will be the bridge between the clinical site and the research study, ensuring that all activities are conducted safely and effectively. Your primary duties will include:

  • Clinical Trial Coordination: Actively assist and manage day-to-day clinical trial activities to ensure adherence to study protocols.
  • Patient Management: Oversee patient recruitment, facilitate patient interactions, conduct follow-up visits, and ensure a high standard of patient care throughout the study.
  • Data Management: Perform accurate collection, entry, and verification of clinical trial data.
  • Documentation & Compliance: Maintain comprehensive study files, source documentation, and regulatory records. You will be responsible for ensuring that all site activities remain in strict compliance with ICH-GCP (International Council for Harmonisation – Good Clinical Practice) guidelines and specific study protocols.
  • Investigator Support: Provide administrative and operational support to Principal Investigators during site visits and throughout the study duration.

Requirements

To be successful in this role, candidates should possess the following qualifications and attributes:

  • Educational Background: A degree in M.Pharm, B.Pharm, Pharm.D, M.Sc, or B.Sc (Life Sciences).
  • Industry Knowledge: A solid understanding of clinical research principles and the fundamentals of clinical trials.
  • Communication Skills: Fluency in English, Hindi, and local regional languages is essential to effectively communicate with patients and team members.
  • Core Competencies:
    • Strong attention to detail and a high level of accuracy.
    • Excellent organizational skills for data and document management.
    • A professional, compassionate approach to patient handling.
    • A commitment to maintaining strict ethical and regulatory standards.

Benefits

Working with Shree Clinical Research Services offers more than just a job; it provides a comprehensive learning environment for your future career growth. Benefits include:

  • Industry Entry: An excellent platform for freshers to break into the clinical research industry.
  • Hands-on Experience: Exposure to real-time clinical trial operations, patient data handling, and complex regulatory documentation.
  • Career Advancement: This role serves as a stepping stone toward advanced roles in the field, such as Clinical Research Associate (CRA), Clinical Trial Coordinator (CTC), or specialized Data Management positions.

How to Apply

If you are a motivated individual ready to contribute to the advancement of medical science, we would love to hear from you. Please submit your updated Curriculum Vitae (CV) to our recruitment team to initiate the application process.

(Note: Please ensure your CV highlights your academic background and any relevant internship or work experience in the life sciences sector.)