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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