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Clinical Research Coordinator

3 weeks ago

Miami, Florida, United States Diverse Clinical Research, LLC Full time

We are seeking a Clinical Research Coordinator to join our team and play a key role in managing clinical studies across multiple therapeutic areas. This position is ideal for an organized, driven professional who thrives in a collaborative research environment.

Key Responsibilities


• Gain thorough knowledge of study protocols in collaboration with the Principal Investigator (PI) and Site Director prior to study activation


• Develop, review, and refine source documents before study launch


• Design and implement recruitment strategies in coordination with primary care providers, nursing staff, and the Recruitment Manager


• Address protocol clarifications with the PI and Site Director


• Collaborate with sponsors and investigators to ensure protocol compliance


• Support enrollment initiatives and study execution


• Assist with the development and review of Standard Operating Procedures (SOPs)


• Execute study activities as assigned and supervised by site leadership


• Manage IRB submissions, renewals, and maintain organized regulatory documentation


• Screen, enroll, and coordinate visits for study participants


• Obtain informed consent and document communications with sponsors, IRBs, labs, and regulatory agencies


• Maintain accurate and complete study records, including regulatory files, consent forms, drug accountability logs, and correspondence


• Perform study close-out procedures and ensure proper record storage


• Complete additional duties as needed to support the organization's mission and goals

Minimum Qualifications


• Minimum 2 years of clinical research experience, including clinical trials and regulatory documentation


• Strong organizational and communication skills with the ability to manage multiple priorities


• High School Diploma required; college degree preferred


• 2–4 years of experience as a Clinical Research Coordinator or CRC certification

Preferred Qualifications


• CCRC or CCRP certification


• Knowledge of Good Clinical Practice (GCP) and FDA regulations


• Experience with EMR and CTMS systems


• Ability to work independently and in a fast-paced team environment


• Strong problem-solving and critical-thinking skills


• Bilingual in Spanish (preferred)


Why Join Diverse Clinical Research?


• Mission-driven organization focused on diversity and inclusion


• Opportunity to impact underrepresented communities through research


• Collaborative and supportive clinical research environment

Apply today and help advance equitable clinical research.