What are the responsibilities and job description for the Lead Clinical Research Coordinator position at Total Health and Research Center?
Company Description
Total Health and Research Center, LLC (THRC) is a premier clinical research facility located in Homestead and Kendall, Florida. We partner with one of the largest vertically integrated healthcare providers in S. Florida with over 200,000 patients in capitation. No patient recruiting needed. Dedicated to advancing medical science and improving patient outcomes, we conduct innovative research studies, offer specialized diagnostics, and provide personalized health solutions. Our multidisciplinary team collaborates with leading pharmaceutical companies, CROs, and healthcare partners to conduct Phase I–IV clinical trials across a variety of therapeutic areas. Our facility features state-of-the-art diagnostic tools, private exam rooms, and dedicated monitoring spaces for sponsors and CROs. We aim to bridge the gap between research and real-world care, providing patients with access to cutting-edge treatments while contributing to medical advancements.
Role Description
This is a full-time, on-site role for a Lead Clinical Research Coordinator based in Homestead, Florida. The Lead Clinical Research Coordinator will manage and oversee clinical trials and other staff to ensure compliance with protocols, regulatory requirements, and good clinical practices. Daily tasks include enrolling participants, obtaining informed consent, collecting and recording data, coordinating with medical staff, and managing study documentation. The role also involves monitoring participant safety, resolving issues, and communicating with sponsors and CROs efficiently.
Qualifications
- Leadership and supervisory experience
- Experience with Informed Consent processes and protocols
- Proficient in conducting and managing Clinical Trials
- Strong Clinical Research Experience
- Excellent organizational and communication skills
- Ability to work independently and manage multiple tasks
- Bachelor’s degree in a related scientific field or equivalent experience
- Certification in Clinical Research (ACRP or SOCRA) is a plus
- Experience in managing Phase I–IV clinical trials is beneficial
- Experience in Oncology trials is a plus