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    Crc- Clinical Research Co-Ordinator-Fresher

    Kite-Ai Technologies
    Freshers years
    Not Disclosed
    Kolhapur Nagpur Pune
    10 March 7, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm Skills: Communication Skills, Interpersonal Skill, Technical Skill

    Job description

    aaRole & responsibilities

     

     

    1. Study Planning and Initiation: Assist in the development of study protocols, case report forms (CRFs), and other study documents. Coordinate with investigators, sponsors, and regulatory authorities to obtain necessary approvals.
    2. Participant Recruitment and Screening: Identify and screen potential participants for eligibility according to the study protocol. Explain the study to potential participants and obtain informed consent.
    3. Study Coordination: Coordinate study visits and procedures, including scheduling, specimen collection, and data collection. Ensure that study procedures are conducted according to protocol and GCP guidelines.
    4. Data Collection and Management: Collect, record, and manage study data accurately and securely. Maintain study records and ensure data quality and integrity.
    5. Safety Reporting: Monitor participant safety throughout the study and report adverse events and other safety issues to the appropriate authorities.
    6. Regulatory Compliance: Ensure compliance with regulatory requirements, including GCP, FDA regulations, and local laws. Maintain study documentation and records as per regulatory standards.
    7. Communication: Communicate regularly with study participants, investigators, sponsors, and other study staff. Provide updates on study progress and address any issues or concerns.
    8. Quality Assurance: Assist in quality assurance activities, such as internal audits and monitoring visits, to ensure that the study is conducted according to protocol and regulatory requirements.
    9. Budget and Resource Management: Assist in managing study budgets and resources, including ordering study supplies and managing study-related expenses.
    10. Training and Development: Stay updated with current regulations, guidelines, and best practices in clinical research. Participate in relevant training and professional development activities.
    11. Ethical Conduct: Ensure that the study is conducted ethically and that participant confidentiality is maintained at all times.
    12. Closeout Activities: Assist in study closeout activities, including final data collection, documentation, and archiving.


     

    Preferred candidate profile: Any Graduate or a PostGraduate, looking to learn and establish their career in Clinical Research.


     

    Perks and benefits: Annual CTC- 1.5 LPA to 2.4 LPA + Travelling Allowance + Learning Allowance + Yearly Bonus.

     

    Interested Candidates can also share their profiles on KITE-Ai Whatsapp +91 73855 18324 or email their resumes to careers@kite-ai.com.


     

    Role: Clinical Assistant

    Industry Type: Clinical Research / Contract Research

    Department: Healthcare & Life Sciences

    Employment Type: Full Time, Permanent

    Role Category: Other Hospital Staff

    Education

    UG: BAMS in Any Specialization, BDS in Any Specialization, BVSC in Any Specialization, BHMS in Any Specialization, B.Sc in Bio-Chemistry, Biology, Microbiology, Nursing, Chemistry, Zoology, B.Pharma in Any Specialization

    PG: MS/M.Sc(Science) in Biotechnology, Bio-Chemistry, Biology, Chemistry, M.Pharma in Any Specialization

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