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Join a fast-growing clinical research team driving innovation in
neurology, cardiology, and infectious disease
trials. As a
Clinical Research Coordinator , you’ll play a key role in managing studies from start-up through close-out, ensuring every detail meets the highest standards of data quality, ethics, and patient care. Salary
- Competitive + quarterly bonus + academy for gaining certifications to develop What You’ll Do
Coordinate and oversee all aspects of clinical trials — from patient screening to study close-out. Obtain informed consent, manage subject visits, and maintain complete, compliant documentation. Ensure accuracy in source data and eCRFs while meeting sponsor timelines. Report and document adverse events in line with GCP and IRB requirements. Collaborate with investigators, sponsors, and internal teams to keep studies on track. Keep all research activity in full compliance with
GCP, ICH, IRB , and company SOPs. What We’re Looking For
2+ years’ experience
as a Clinical Research Coordinator (pharma or device). Strong working knowledge of
clinical trial processes, GCP, and ICH guidelines . Excellent communication, organization, and multitasking skills. Proficiency in
Office365
and
electronic data capture systems . Bachelor’s degree in a science or healthcare field preferred. Flexible schedule — occasional evenings/weekends and travel required. Seniority level
Mid-Senior level Employment type
Full-time Job function
Project Management Industries
Pharmaceutical Manufacturing and Biotechnology Research Location: Sumter County, FL | Salary: $61,800 - $66,950
#J-18808-Ljbffr
neurology, cardiology, and infectious disease
trials. As a
Clinical Research Coordinator , you’ll play a key role in managing studies from start-up through close-out, ensuring every detail meets the highest standards of data quality, ethics, and patient care. Salary
- Competitive + quarterly bonus + academy for gaining certifications to develop What You’ll Do
Coordinate and oversee all aspects of clinical trials — from patient screening to study close-out. Obtain informed consent, manage subject visits, and maintain complete, compliant documentation. Ensure accuracy in source data and eCRFs while meeting sponsor timelines. Report and document adverse events in line with GCP and IRB requirements. Collaborate with investigators, sponsors, and internal teams to keep studies on track. Keep all research activity in full compliance with
GCP, ICH, IRB , and company SOPs. What We’re Looking For
2+ years’ experience
as a Clinical Research Coordinator (pharma or device). Strong working knowledge of
clinical trial processes, GCP, and ICH guidelines . Excellent communication, organization, and multitasking skills. Proficiency in
Office365
and
electronic data capture systems . Bachelor’s degree in a science or healthcare field preferred. Flexible schedule — occasional evenings/weekends and travel required. Seniority level
Mid-Senior level Employment type
Full-time Job function
Project Management Industries
Pharmaceutical Manufacturing and Biotechnology Research Location: Sumter County, FL | Salary: $61,800 - $66,950
#J-18808-Ljbffr