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Senior Clinical Trials Coordinator

2 months ago

Fayetteville, Georgia, United States Medix™ Full time

Join our innovative team at Medix™ as a Clinical Research Coordinator. In this pivotal role, you will lead and manage essential clinical trials that contribute to groundbreaking medical advancements. We pride ourselves on fostering a collaborative and inclusive environment that supports your professional journey. Be part of our commitment to enhancing healthcare outcomes and transforming patient lives.

KEY RESPONSIBILITIES

1. Oversee the execution of various intricate clinical research protocols.

2. Collaborate with the Principal Investigator and Clinical Research Manager to develop standard operating procedures and templates.

3. Manage eligibility assessments and recruitment strategies to optimize participant enrollment.

4. Ensure compliance in sample processing, packaging, and shipping in accordance with study protocols and regulatory standards.

5. Design and implement monitoring strategies to document and address any unexpected events or protocol deviations.

6. Take charge of protocol execution and study advancement, keeping all stakeholders informed of progress.

7. Coordinate site visits and manage both internal and external audit processes as required.

8. Facilitate research team meetings to ensure effective communication across multidisciplinary teams.

9. Synchronize study visits, procedures, and clinical assessments with data collection timelines to ensure smooth participant progression through the study.

10. Adhere to the fundamental requirements set forth by international, national, and local regulatory agencies.

EMPLOYEE BENEFITS

  • Comprehensive Medical, Dental, and Vision insurance
  • Paid Time Off (PTO)
  • Commuter Benefits
  • 401k plan with employer matching
  • Adoption Assistance and Caregiver Resources and more