Full Job Description
Clinical Research Nurse Practitioner
The Clinical Research Nurse Practitioner will serve as a key member of the clinical research team in a clinical trial setting. As an advanced practice medical professional, you will be responsible for ensuring the highest standards of patient care throughout the clinical trial process. Your primary role will involve conducting physical examinations, interpreting lab test results, and overseeing patients’ health while working closely with other healthcare professionals. You will be expected to provide both direct medical care and education to patients, as well as contribute to the advancement of clinical knowledge through research and professional collaboration.
Key Responsibilities:
- Perform physical examinations and assess patients’ medical histories in a clinicaltrial setting.
- Interpret and analyze lab test results to monitor patient health and make clinicaldecisions.
- Oversee and monitor patient health status throughout the trial, ensuring patientsafety and compliance with protocol requirements.
- Educate patients and their families on the clinical trial process, including treatmentplans and potential risks.
- Administer medications and oversee the safe administration of medications,ensuring adherence to clinical protocols.
- Conduct medical procedures such as venipuncture, IV line placement, and othertasks as required by the study protocol.
- Monitor and provide safety observations during and after medication administrationto ensure patient well-being and manage any adverse reactions.
- Collaborate with the primary investigator and other members of the clinical trialteam to ensure the effective execution of study protocols.
- Ensure proper documentation of clinical data in accordance with regulatory andethical standards.
- Maintain a clear, open line of communication with other healthcare professionals toensure integrated, patient-centered care.
- Participate in regular meetings and discussions to review patient progress, studyoutcomes, and other relevant clinical findings.
- Stay informed on the latest developments in medical research and clinicalpractices, advancing personal and professional knowledge.
Additional Responsibilities:
This job description includes core responsibilities but is not limited to the items listed above. The Sub-Investigator may be assigned additional duties as necessary to support the clinical trial and research efforts. These may include, but are not limited to, assisting in
protocol design, supporting regulatory submissions, mentoring junior staff, and participating in educational and research initiatives.
Medical Specialties:
Primary Care
License/Certification Requirements:
Nurse Practitioner Medical License or
Physician Assistant License (Required)
Qualifications:
Proven experience in a clinical or healthcare setting, with a focus on patient careand medical research.
Strong problem-solving skills and the ability to make sound clinical decisions.
Excellent communication skills, with the ability to effectively interact with patients,families, and other healthcare professionals.
Detail-oriented with a commitment to accuracy in medical documentation andpatient monitoring.
Team player with a positive attitude and dedication to advancing clinical knowledgeand patient care.
A strong passion for clinical research, patient advocacy, and advancing medicalpractices.
Preferred Skills:
Previous experience in clinical trials or research settings.
Familiarity with regulatory guidelines and ethical practices in clinical research.
Ability to educate patients and staff on clinical protocols and research procedures.
Work Environment:
Collaborative and dynamic clinical setting.
Opportunities for professional development, continuing education, and research advancement.
Job Type: Full-time
Pay: From $120,000.00 per year
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Flexible spending account
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Vision insurance
Work Location: In person
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