Clinical Research Coordinator (CRC)

Company Description Access Health Care Physicians, LLC is a multi-service medical facility that provides in-house diagnostic testing and comprehensive medical services to the community. The organization is committed to using advanced technology and delivering high-quality, patient-centered care. Team members work in an environment that prioritizes patient needs through same-day appointments, reduced waiting times, and attentive communication. Access Health Care Physicians, LLC offers a broad range of specialties, helping patients receive coordinated care with fewer delays and administrative barriers. This setting provides clinical professionals with opportunities to contribute meaningfully to patient outcomes and practice innovation.

Role Description The Clinical Research Coordinator (CRC) is a full-time, on-site role based in Brooksville, FL. The CRC will coordinate and oversee clinical trials, including participant recruitment, screening, and enrollment, while ensuring adherence to study protocols and regulatory requirements. Daily responsibilities include obtaining and documenting informed consent, scheduling and conducting study visits, collecting and entering data, and maintaining accurate source documents and regulatory binders. The CRC will collaborate with investigators, clinical staff, sponsors, and monitors to support study timelines, manage study supplies, and address queries or deviations. This role also involves monitoring participant safety, reporting adverse events, and supporting quality assurance activities to maintain compliance and high standards of care.

Qualifications

• Candidates should possess strong clinical research experience and a solid understanding of clinical trials.
• Candidates should possess skills in informed consent processes and ethical conduct of human subject research.
• Candidates should possess knowledge of study protocol implementation and research best practices.
• Relevant experience with regulatory documentation, data collection, and source data verification is beneficial.
• Strong organizational skills, attention to detail, and the ability to manage multiple studies or tasks simultaneously.
• Effective written and verbal communication skills for interacting with participants, clinical teams, and sponsors.
• Ability to work on-site in Brooksville, FL and collaborate within a multidisciplinary healthcare environment.
• Preferred: Bachelor’s degree in a health-related field (such as Nursing, Biology, or Public Health) and certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA) or willingness to obtain certification.