Join KV Clinical Research: Clinical Research Coordinator Vacancy

    • Raipur
    • ₹30000 INR / Month


    Embark on an exciting career journey with KV Clinical Research Pvt Ltd, a renowned name in the field of clinical research. We are currently seeking passionate individuals to join us as Clinical Research Coordinators (CRC) for oncology trials at our Raipur, C.G. location. If you possess a background in B & M Pharmacy, Pharma D, or hold a diploma in clinical research, this could be the opportunity you’ve been looking for. Join us in our mission to contribute to groundbreaking research and make a difference in the field of healthcare.

    About the Company (KV Clinical Research Pvt Ltd):

    KV Clinical Research Pvt Ltd is a leading player in the realm of clinical research, committed to conducting ethical and high-quality trials that pave the way for medical advancements. Founded with a vision to transform healthcare through innovation and excellence, we specialize in oncology trials and strive to bring novel therapies to patients in need. Our team comprises dedicated professionals driven by a shared passion for improving patient outcomes and advancing medical science.

    Company Vacancies List:

    Explore the available position at KV Clinical Research Pvt Ltd:

    • Clinical Research Coordinator (CRC)

    Job Description:

    Role: Clinical Research Coordinator

    Industry Type: Clinical Research

    Department: Oncology Trials

    Employment Type: Full-time

    Role Category: Research & Development

    Location: Raipur, C.G.

    Qualifications and Requirements:

    • Educational Background: B & M Pharmacy, Pharma D, or Diploma in Clinical Research
    • Experience: Experience in oncology trials preferred
    • Proficiency in English, Hindi, and regional languages
    • Strong organizational and communication skills
    • Ability to work effectively in a team and manage multiple tasks simultaneously

    About the Department & Responsibilities:

    As a Clinical Research Coordinator, you will play a pivotal role in the successful execution of oncology trials. Your responsibilities will include:

    • Coordinating and overseeing all aspects of clinical research studies, ensuring compliance with protocols and regulatory requirements
    • Recruiting and screening eligible participants for clinical trials
    • Collecting and maintaining accurate and complete study documentation
    • Collaborating with investigators, sponsors, and other stakeholders to facilitate study activities
    • Monitoring participant safety and adherence to study protocols
    • Contributing to data analysis and reporting of study results

    How to Apply:

    Ready to take the next step in your career? Send your CV to [email protected] and be part of our mission to drive innovation in clinical research. To learn more about us and apply online, visit

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