Nurse Practitioner – Oncology Clinical Research

TO APPLY:

Please submit your CV and a brief cover letter outlining your oncology and clinical research experience to muzammil@patientcareclinicalresearch.com

ABOUT US:

We are a dedicated oncology clinical research site committed to advancing cancer care through cutting-edge clinical trials. Our team works closely with sponsors, CROs, and principal investigators to bring novel therapies to patients in our community. We are currently seeking an experienced Nurse Practitioner (NP) with a background in oncology and clinical research to join our team on an hourly basis.

POSITION OVERVIEW:

The Nurse Practitioner will play a vital role in the conduct of oncology clinical trials, working collaboratively with the Principal Investigator and research team to ensure protocol compliance, patient safety, and high-quality data collection. This position offers flexibility and the opportunity to work in a dynamic, patient-centered research environment.

KEY RESPONSIBILITIES:

Clinical Research Duties:

• Assist the Principal Investigator in screening, enrolling, and managing patients in oncology clinical trials
• Conduct study visits, including vital signs, physical assessments, and adverse event monitoring
• Administer investigational products (oral, IV, subcutaneous) per protocol requirements
• Perform and coordinate protocol-required procedures (e.g., ECGs, lab draws, tumor assessments)
• Educate patients and families about study participation, potential risks, and benefits
• Monitor and manage trial-related toxicities in collaboration with the PI

Regulatory & Documentation:

• Ensure accurate and timely source documentation and electronic case report form (eCRF) completion
• Assist with query resolution and data clarification
• Maintain compliance with ICH-GCP guidelines, FDA regulations, and institutional policies
• Support informed consent process, ensuring patient understanding and proper documentation

Coordination & Collaboration:

• Communicate effectively with research coordinators, data managers, and sponsor monitors
• Participate in site initiation visits, monitoring visits, and close-out visits
• Assist with preparation for audits and regulatory inspections

QUALIFICATIONS:

Required:

• Current, unrestricted Nurse Practitioner (NP) license in [State]
• Master's degree in Nursing (MSN) from an accredited program
• National certification as a Nurse Practitioner (AANC or AANP)
• Minimum 2 years of clinical experience in oncology (medical oncology, hematology-oncology, or infusion setting)
• Familiarity with clinical trial terminology and research operations
• Strong clinical assessment and patient communication skills
• Proficiency with electronic medical records (EMR) and basic computer applications

Preferred:

• Prior experience working in clinical research (industry-sponsored trials, cooperative group studies, or investigator-initiated research)
• Knowledge of ICH-GCP guidelines and FDA regulations
• Certification in Clinical Research (SoCRA, ACRP) is a plus
• Experience with oncology trial populations (solid tumors, hematologic malignancies, immunotherapy, targeted therapy)
• Chemotherapy/biotherapy certification

SCHEDULE:

• Flexible hourly schedule
• Hours will vary based on study visit volume and patient needs
• Ideal for candidates seeking supplemental income or work-life balance

WHY JOIN US?

• Opportunity to work at the forefront of oncology drug development
• Supportive, collaborative team environment
• Flexible scheduling with competitive hourly pay
• Make a meaningful impact in the lives of cancer patients through access to novel therapies

TO APPLY:

Please submit your CV and a brief cover letter outlining your oncology and clinical research experience to muzammil@patientcareclinicalresearch.com

We are an equal opportunity employer and value diversity at our site. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Pay: $60.00 per hour

Work Location: In person