What are the responsibilities and job description for the Clinical Research Coordinator position at Diverse Clinical Research, LLC?
Company Description
Diverse Clinical Research, LLC is a multispecialty research site facility located in the Miami area, dedicated to delivering high-quality clinical research services. Established by Aramis Rodriguez, APRN, AGACNP-BC, the organization prioritizes the safety and well-being of its volunteers while ensuring reliable data for research sponsors. Committed to adhering to good clinical practice guidelines, Diverse Clinical Research collaborates with a network of medical centers in the Miami area for innovative medical care. Its location, just 1.3 miles from the Turnpike, ensures easy accessibility to nearby hospitals, clinical practices, and specialists.
Role Description
This is a full-time, on-site position based in Miami, FL, for a Clinical Research Coordinator. The Clinical Research Coordinator will manage day-to-day operational aspects of clinical trials, including assisting with informed consent, ensuring protocol adherence, overseeing participant activities, collecting clinical data, and maintaining accurate and confidential records. The role also involves collaborating with investigators, sponsors, and regulatory authorities to ensure compliance with clinical research regulations and standards.
Qualifications
- Expertise in Clinical Research, including Clinical Trials and Clinical Research Experience
- Proficiency in understanding and implementing study Protocols
- Experience with obtaining and documenting Informed Consent
- Strong organizational, communication, and interpersonal skills
- Knowledge of Good Clinical Practice (GCP) guidelines and applicable regulatory standards
- Bachelor’s degree in a related field or equivalent clinical experience
- Certified Clinical Research Coordinator (CCRC) or similar certification is a plus
- Fluency in English; bilingual proficiency in Spanish is highly advantageous