What are the responsibilities and job description for the Clinical Research Coordinator position at Diverse Clinical Research, LLC?
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.