SoTalent
Lead Clinical Research Coordinator (Onsite)
Miami, FL
About the Role This position offers the opportunity to lead multiple clinical studies within a dynamic research environment. The Lead Clinical Research Coordinator oversees the administration, coordination, and successful execution of clinical trials involving human subjects. You’ll ensure studies are conducted smoothly, ethically, and in compliance with protocol requirements — from patient recruitment to data management and regulatory oversight.
Key Responsibilities
Serve as the main point of contact and subject-matter expert for assigned studies.
Oversee all aspects of clinical trial conduct including patient screening, enrollment, and data collection.
Maintain accurate patient and study documentation for sponsors, CROs, and regulatory bodies.
Review participant eligibility and ensure proper consent procedures.
Manage protocol amendments, reporting, and compliance with regulatory standards.
Provide mentorship, training, and guidance to junior coordinators and research assistants.
Prepare study metrics, enrollment reports, and regulatory documentation.
Qualifications
Bachelor’s degree and 5+ years of research experience, or 9+ years of equivalent research experience.
Clinical Research Certification (SOCRA or ACRP: CCRC, CCRP, CRA) required within 1 year of hire.
Advanced understanding of clinical research protocols, compliance, and data management.
Strong communication and organizational skills, with excellent attention to detail.
Bilingual in English/Spanish preferred.
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About the Role This position offers the opportunity to lead multiple clinical studies within a dynamic research environment. The Lead Clinical Research Coordinator oversees the administration, coordination, and successful execution of clinical trials involving human subjects. You’ll ensure studies are conducted smoothly, ethically, and in compliance with protocol requirements — from patient recruitment to data management and regulatory oversight.
Key Responsibilities
Serve as the main point of contact and subject-matter expert for assigned studies.
Oversee all aspects of clinical trial conduct including patient screening, enrollment, and data collection.
Maintain accurate patient and study documentation for sponsors, CROs, and regulatory bodies.
Review participant eligibility and ensure proper consent procedures.
Manage protocol amendments, reporting, and compliance with regulatory standards.
Provide mentorship, training, and guidance to junior coordinators and research assistants.
Prepare study metrics, enrollment reports, and regulatory documentation.
Qualifications
Bachelor’s degree and 5+ years of research experience, or 9+ years of equivalent research experience.
Clinical Research Certification (SOCRA or ACRP: CCRC, CCRP, CRA) required within 1 year of hire.
Advanced understanding of clinical research protocols, compliance, and data management.
Strong communication and organizational skills, with excellent attention to detail.
Bilingual in English/Spanish preferred.
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