Hybrid Certified Registered Nurse Practitioner / CRC
On-siteBirmingham, Alabama, United States
Job Summary
Conduct comprehensive patient assessments, diagnose and manage acute and chronic conditions, and prescribe medications within the Certified Registered Nurse Practitioner scope. Simultaneously serve as the primary coordinator for clinical trials from startup through closeout, screening participants, collecting data, and ensuring compliance with FDA and GCP guidelines. Manage study visits, process laboratory specimens, report adverse events, and reconcile data in electronic systems. This hybrid role bridges direct patient care and research operations at an outpatient clinic and research setting, requiring occasional travel for investigator meetings.
Required Qualifications
- Current Certified Registered Nurse Practitioner (CRNP) license in Alabama (or applicable state)
- Master's or Doctoral degree in Nursing
- Current DEA registration and prescriptive authority
- Minimum 2 years of clinical practice experience
- Minimum 1 year of clinical research experience or equivalent research exposure
- Knowledge of GCP, FDA regulations, and human subject protection requirements
- Strong organizational and project management skills
- Proficiency with EMR and Microsoft Office applications
- Excellent communication and interpersonal skills
- Ability to stand, walk, and sit for extended periods
- Ability to occasionally lift and move up to 25 pounds
- Dexterity required for clinical procedures, data entry, and specimen handling
Desired Qualifications
- Certification as a Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP)
- Experience in industry-sponsored clinical trials
- Therapeutic area experience in nephrology, oncology, cardiology, endocrinology, gastroenterology, or vaccines
- Experience with EDC systems such as Medidata Rave, Veeva, or Oracle Inform
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