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    Clinical Research Coordinator

    Fortis
    0-3 years
    Not Disclosed
    Mohali
    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

    Fortis Healthcare Ltd is looking for Clinical Research Coordinator to join our dynamic team and embark on a rewarding career journey

    • We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our research team
    • The successful candidate will play a key role in the planning, coordination, and execution of clinical research studies
    • This position requires strong organizational skills, attention to detail, and the ability to work collaboratively with research teams and study participants

    Responsibilities:

    • Study Coordination:Coordinate and manage all aspects of clinical research studies, including participant recruitment, scheduling, and follow-up visits
    • Ensure compliance with study protocols, regulatory requirements, and ethical standards
    • Participant Recruitment and Informed Consent:Develop strategies for participant recruitment and enrollment in clinical trials
    • Obtain informed consent from eligible participants and ensure a clear understanding of study requirements
    • Data Collection and Management:Collect and record accurate and timely data from study participants
    • Maintain organized and complete study records, ensuring data integrity and confidentiality
    • Collaboration with Investigators:Work closely with principal investigators, sub-investigators, and other research team members
    • Coordinate study meetings, prepare documentation, and facilitate communication among team members
    • Regulatory Compliance:Ensure compliance with regulatory requirements, Institutional Review Board (IRB) guidelines, and Good Clinical Practice (GCP) standards
    • Prepare and submit regulatory documents as required
    • Monitoring and Quality Assurance:Monitor and audit study processes to ensure adherence to protocols and regulatory standards
    • Implement quality assurance measures to maintain high standards in data collection and management
    • Budget and Resource Management:Assist in budget planning for clinical research studies
    • Manage and allocate resources efficiently to support study activities
    • Communication with Study Participants:Communicate effectively with study participants, addressing inquiries and providing ongoing support
    • Ensure participant safety and welfare throughout the duration of the study

    Role: Clinical research Scientist

    Industry Type: Medical Services / Hospital

    Department: Research & Development

    Employment Type: Full Time, Permanent

    Role Category: Pharmaceutical & Biotechnology

    Education

    UG: Any Graduate

    PG: Any Postgraduate

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