Clinical Research Coordinator

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.