ClinLab Staffing
Clinical Research Coordinator at ClinLab Staffing Aventura, FL
ClinLab Staffing, Florida, New York, United States
Overview
Clinical Research Coordinator job at ClinLab Staffing. Aventura, FL.
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.
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)
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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.
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)
#J-18808-Ljbffr