ClinLab Staffing
Clinical Research Coordinator
Job Summary We are seeking an experienced and detail-oriented Clinical Research Coordinator (CRC) to join our team. This role is ideal for candidates with at least 2 years of clinical research experience who are ready to take ownership of trial coordination in a high-performing, supportive environment. The CRC will work closely with investigators, participants, and sponsors to ensure accurate, timely, and compliant execution of clinical trials.
Note:
Only candidates currently living in South Florida will be considered. Relocation assistance and visa sponsorship are not available.
Key Responsibilities Coordinate and manage day-to-day activities for assigned clinical trials Schedule and conduct study visits, ensuring adherence to protocols Interview and consent participants, administer assessments, and maintain accurate study records Dispense and account for investigational product according to study protocols Enter data into EDC and CTMS systems; resolve queries in a timely manner Maintain regulatory compliance and documentation readiness Communicate with sponsors, monitors, and internal teams to ensure timelines are met Collaborate with colleagues and external partners to support study goals
Qualifications At least 2 years of clinical research experience Strong administrative, organizational, and multitasking skills with attention to detail Experience with EDC platforms, CTMS, and Microsoft Office (Word, Excel, Outlook) Knowledge of FDA, GCP, and ICH guidelines Ability to work independently in a fast-paced environment Excellent interpersonal and communication skills with the ability to engage participants, physicians, and sponsors Bachelor’s degree or equivalent work experience
Preferred: Previous experience in neurology or CNS trials Bilingual (Spanish/English) highly preferred CCRP or ACRP certification
Why Join Collaborative team environment committed to advancing research Competitive compensation and benefits Opportunities for growth and professional development
Benefits 401(k) with matching Medical, dental, vision, and life insurance Health savings and flexible spending accounts Disability insurance Paid time off, parental leave, and family leave Paid training and professional development support Mileage and travel reimbursement Referral program
Schedule Monday–Friday, day shift (8-hour shifts, full-time) On-site role (South Florida)
Job Summary We are seeking an experienced and detail-oriented Clinical Research Coordinator (CRC) to join our team. This role is ideal for candidates with at least 2 years of clinical research experience who are ready to take ownership of trial coordination in a high-performing, supportive environment. The CRC will work closely with investigators, participants, and sponsors to ensure accurate, timely, and compliant execution of clinical trials.
Note:
Only candidates currently living in South Florida will be considered. Relocation assistance and visa sponsorship are not available.
Key Responsibilities Coordinate and manage day-to-day activities for assigned clinical trials Schedule and conduct study visits, ensuring adherence to protocols Interview and consent participants, administer assessments, and maintain accurate study records Dispense and account for investigational product according to study protocols Enter data into EDC and CTMS systems; resolve queries in a timely manner Maintain regulatory compliance and documentation readiness Communicate with sponsors, monitors, and internal teams to ensure timelines are met Collaborate with colleagues and external partners to support study goals
Qualifications At least 2 years of clinical research experience Strong administrative, organizational, and multitasking skills with attention to detail Experience with EDC platforms, CTMS, and Microsoft Office (Word, Excel, Outlook) Knowledge of FDA, GCP, and ICH guidelines Ability to work independently in a fast-paced environment Excellent interpersonal and communication skills with the ability to engage participants, physicians, and sponsors Bachelor’s degree or equivalent work experience
Preferred: Previous experience in neurology or CNS trials Bilingual (Spanish/English) highly preferred CCRP or ACRP certification
Why Join Collaborative team environment committed to advancing research Competitive compensation and benefits Opportunities for growth and professional development
Benefits 401(k) with matching Medical, dental, vision, and life insurance Health savings and flexible spending accounts Disability insurance Paid time off, parental leave, and family leave Paid training and professional development support Mileage and travel reimbursement Referral program
Schedule Monday–Friday, day shift (8-hour shifts, full-time) On-site role (South Florida)