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Clinical Research Nursing Coordinator
2 months ago
Position Summary
About Our Organization
With over two decades of experience, Clinical Research of West Florida, Inc. has successfully engaged with more than 10,000 patients and conducted over 1,000 Phase I-IV clinical trials. Our model as a dedicated research facility has gained recognition across the nation. We take pride in being pioneers in delivering high-quality performance and exceptional patient satisfaction.
Important Note for Applicants: Candidates lacking clinical research experience will not be considered. Only those with a minimum of two years of relevant experience will be evaluated for this role. We appreciate your understanding.
Role of Clinical Research Nursing Coordinator
The Clinical Research Nursing Coordinator will oversee clinical trials under the guidance of the Principal Investigator(s) at CRWF, ensuring compliance with good clinical practice standards, federal and state regulations, institutional review board (IRB) protocols, and CRWF Standard Operating Procedures.
Key Responsibilities:
- Recruiting study participants
- Screening and consenting patients
- Conducting clinical follow-ups as per study protocols
- Completing source documentation
- Reporting serious adverse events
- Managing drug dispensing and accountability
- Maintaining subject enrollment logs
The Clinical Research Nursing Coordinator will engage directly with patients, study sponsors, Site Director, Physicians, Co-Coordinators, Lab Manager, EDC Manager, and other personnel at CRWF.
Additional Responsibilities:
- Ensuring confidentiality and security of patient information
- Reviewing medical records for patient history and eligibility
- Informing sponsors of patient non-compliance or drug-related issues
- Drawing, processing, and packaging laboratory samples as necessary
- Interpreting laboratory results and communicating abnormal findings to the investigator and patient
Qualifications: Candidates must possess the ability to understand complex protocols, work autonomously, develop source documents in accordance with protocols, manage multiple ongoing tasks, and thrive in a dynamic, collaborative environment. Effective communication skills with both subjects and staff are essential.
Preferred Experience:
At least 2 years of clinical research experience, including GCP Training.
Preferred Certifications (not mandatory): CCRP (Clinical Research Professional) or CCRC (Clinical Research Coordinator).
Required Licensure: LPN or RN.
CRWF operates multiple offices and is recognized as a leader in clinical research. We have facilitated numerous Phase I-IV studies across various therapeutic areas, committed to delivering outstanding patient care with a team of board-certified/eligible physicians and highly trained clinical staff.
Equal Opportunity Employer. Competitive salary package offered.
Job Type: Full-time
Salary: Ranges from $70,000 to $90,000 annually, based on education and experience.
Work Arrangement: In-person
Benefits:
- 401(k) matching
- Paid time off
Schedule: Monday to Friday
Relocation Requirement: Candidates must be prepared to relocate before commencing work.
