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    Clinical Research Coordinator

    Pragmatic
    1-3 years
    $50/hr - $65/hr
    10 May 20, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Communication Skills, ICD-10 CM, CPT, HCPCS Coding, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Job Description: Clinical Research Coordinator (6-12 Month Contract)

    Position: Clinical Research Coordinator
    Location: Columbia, South Carolina

    About the Company:
    Our partner is a pioneering medical device company specializing in innovative ear tube technology for children. Dedicated to enhancing the quality of life for young patients, their cutting-edge solutions promise safer and more effective treatments.

    Responsibilities:
    As a Clinical Research Coordinator, you will play a pivotal role in advancing pediatric healthcare through clinical research. Your key responsibilities include:

    • Patient Recruitment:

      • Actively recruit and enroll eligible patients into clinical trials.
      • Ensure adherence to protocol requirements and ethical standards.

    • Study Coordination:

      • Coordinate all aspects of clinical trial activities.
      • Schedule patient visits, obtain informed consent, manage study documentation, and coordinate/oversee onsite monitoring visits.

    • Data Management:

      • Maintain Electronic Data Capture (EDC) systems.
      • Ensure accurate and timely entry of study data in compliance with regulatory guidelines.

    • Communication:

      • Serve as a liaison between study participants, healthcare professionals, and study sponsors.
      • Provide clear and compassionate communication throughout the research process.

    • Adverse Event Reporting:

      • Promptly report and document adverse events.
      • Follow established procedures to ensure patient safety.

    • On-Site Presence:

      • Attend clinical cases and planned study visits.
      • Assist in gaining informed consent, performing assessments, and ensuring protocol compliance, particularly in the Columbia, South Carolina area.

    Qualifications:

    • Bachelor’s degree in a related field (e.g., nursing, biology, life sciences).
    • Previous experience in clinical research coordination with medical devices, preferably in a pediatric setting.
    • Strong communication skills with the ability to effectively interact with diverse stakeholders.
    • Detail-oriented mindset with excellent organizational skills.
    • Familiarity with Electronic Data Capture (EDC) systems preferred.
    • Ability to travel locally for on-site study visits within Columbia, South Carolina, and surrounding areas.

    Why Join Us?:

    • Opportunity to contribute to groundbreaking research in pediatric healthcare.
    • Collaborative and supportive work environment.
    • Competitive compensation package.
    • Potential for career advancement within a dynamic industry.

    Apply Now:
    If you’re ready to play a key role in transforming pediatric healthcare and making a difference in the lives of children, apply now! Join us in our mission to revolutionize ear tube technology and shape the future of pediatric medicine.

    Application Instructions:
    Please submit your resume and cover letter detailing your relevant experience and why you’re passionate about this opportunity. We look forward to hearing from you!

    Apply Here: Job Application Link

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