Top 6 Clinical research coordinator Jobs in Saint Augustine Fl

Clinical Research Coordinator
ECN Operating LLC —Jacksonville, FL
- $17 - $25 an hour
- 8 hour shift
- Organizational skills
- In-person
- Communication skills
Quick Apply
4d
Clinical Coordinator Reigistered Nurse
DAVITA —Saint Johns, FL
- Weekends as needed
- Microsoft Word
- CPR Certification
- Nursing
- Paid training
- Health insurance

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Lab Services Coordinator - Clinical Trials Processing Lab
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Participates in data entry and management, quality control, audits and FDA inspections, continuous quality improvement and inventory management of clinical…
Clinical Research Coordinator
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This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…

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Clinical Research Coordinator

ECN Operating LLC
Jacksonville, FL

Quick Apply

Job Details

Full-time
$17 - $25 an hour
4 days ago

Qualifications

Certified Phlebotomy Technician
Organizational skills
Communication skills
Entry level

Full Job Description

Job Summary:

We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.

Key Responsibilities:

Coordinate day-to-day clinical research activities to ensure study protocols are followed.
Recruit, screen, and enroll study participants.
Obtain informed consent and ensure ethical conduct in all study interactions.
Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples).
Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs).
Maintain accurate and timely documentation in case report forms and electronic databases.
Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.
Schedule participant visits and follow-ups; ensure visit windows are met.
Ensure proper storage, handling, and accountability of investigational products, if applicable.
Maintain regulatory documents and assist with IRB submissions.

Qualifications:

Bachelor's degree in a health-related field required.
At least 1–2 years of experience in clinical research preferred.
Phlebotomy certification or MA certification preferred.
Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
Excellent organizational skills and attention to detail.
Strong interpersonal and communication skills.
Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms).
Ability to work independently and as part of a multidisciplinary team.

Preferred Qualifications:

Experience working in clinical trials, especially in a hospital or academic setting.
Familiarity with IRB processes and clinical trial documentation.
Bilingual skills (depending on patient population) may be a plus.

Job Type: Full-time

Work Location: In person

Schedule:

8 hour shift
Monday to Friday
Weekends as needed

Quick Apply

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clinical research coordinator jobs in saint augustine fl

Clinical Research Coordinator

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