Job Overview
We are seeking an experienced and highly motivated Family Nurse Practitioner (FNP-C) to join our clinical research team as a Sub-Investigator (Sub-I) and/or clinical research provider.
This is an excellent opportunity for an FNP with strong clinical experience who is interested in expanding into clinical research, clinical trials, and investigational medicine. The ideal candidate will have strong patient assessment skills, sound clinical judgment, excellent documentation abilities, and a commitment to following research protocols and Good Clinical Practice (GCP) standards.
The Sub-Investigator will work closely with the Principal Investigator (PI), Clinical Research Coordinators, and other members of the research team to ensure the safe, ethical, and accurate conduct of clinical trials.
Key Responsibilities
- Serve as a Sub-Investigator on clinical research studies under the supervision and delegation of the Principal Investigator.
- Conduct medical assessments, physical examinations, medical histories, and clinical evaluations according to study protocols.
- Evaluate patient eligibility and assist with screening and enrollment of qualified study participants.
- Perform and document study-related procedures and assessments within protocol requirements.
- Review medical histories, laboratory results, vital signs, diagnostic findings, and other clinical data.
- Assess and document adverse events (AEs), concomitant medications, and changes in participants' medical conditions.
- Provide appropriate medical care and clinical oversight to research participants throughout the study.
- Collaborate with the PI and research team regarding participant safety, protocol requirements, and medical decision-making.
- Maintain accurate, timely, and complete documentation in the EHR and clinical trial systems.
- Ensure all delegated research activities are performed in compliance with ICH-GCP, FDA regulations, study protocols, and applicable regulatory requirements.
- Participate in investigator meetings, protocol training, site initiation activities, monitoring visits, and other study-related meetings as required.
- Communicate professionally with study participants, sponsors, CROs, monitors, and members of the research team.
- Maintain patient confidentiality and comply with HIPAA and applicable privacy regulations.
- Support recruitment and retention efforts while maintaining ethical standards and protocol compliance.
Clinical Responsibilities
Depending on the candidate's experience and study requirements, responsibilities may include:
- Comprehensive physical examinations and clinical assessments
- Diagnosis and management of acute and chronic conditions
- Medication management and review of concomitant medications
- Venipuncture and other routine clinical procedures
- Assessment of laboratory and diagnostic results
- Patient education and counseling
- Telehealth or follow-up assessments when permitted by the study protocol
- Documentation of clinical findings and medical decision-making
- Recognition and appropriate management or escalation of adverse events
Ideal Candidate
We are particularly interested in FNPs who have:
- Strong clinical experience in Family Medicine, Internal Medicine, Urgent Care, Emergency Medicine, or related specialties
- Experience evaluating and treating diverse adult patient populations
- Excellent clinical assessment and medical decision-making skills
- Strong attention to detail and accurate medical documentation
- Interest in clinical research and investigational medicine
- Ability to understand and follow detailed study protocols
- Excellent communication and interpersonal skills
- Ability to work collaboratively with physicians, investigators, coordinators, and research staff
- Professionalism and a strong commitment to participant safety and ethical research conduct
Previous clinical research experience is preferred but not required. Candidates with strong clinical backgrounds who are interested in transitioning into clinical research are encouraged to apply.
Preferred Qualifications
- Family Nurse Practitioner (FNP-C) certification
- Active and unrestricted Nurse Practitioner license in the applicable state/jurisdiction
- Current DEA registration, if applicable
- Current CPR/BLS certification
- Clinical experience in Family Medicine, Internal Medicine, Urgent Care, Emergency Medicine, or a related field
- Previous clinical research, clinical trial, or investigator experience preferred
- Knowledge of ICH-GCP, FDA regulations, and clinical research processes preferred
- Experience with EHR/EMR systems such as Epic, eClinicalWorks, Athenahealth, Cerner, or similar platforms
- Strong proficiency in medical terminology, clinical documentation, and patient assessment
Why Join Our Clinical Research Team?
This position provides an opportunity to:
- Participate directly in clinical trials and investigational research
- Work alongside experienced Principal Investigators and clinical research professionals
- Gain valuable experience in clinical research and GCP
- Contribute to the development of new therapies and treatment options
- Maintain an active clinical role while expanding your professional experience into research
- Work in a collaborative, patient-centered clinical research environment
How to Apply
If you are an experienced Family Nurse Practitioner interested in becoming involved in clinical research as a Sub-Investigator, we encourage you to apply.
Please submit your resume highlighting your clinical experience, certifications, licenses, and any previous clinical research or investigator experience.
Clinical research experience is a plus, but strong clinical experience and a willingness to learn clinical research are highly valued.
Pay: $35.00 - $60.00 per hour
Benefits:
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Work Location: In person
