Clinical Research Coordinator

Overview

Clinical Research Coordinator

Full-Time | Onsite | Monday – Friday

$72,645.00 - $84,339 per year. The actual hiring rate may vary based on several factors, including your previous work experience, educational background, the responsibilities of the position, and demonstrated performance. These elements help us ensure a fair and competitive offer aligned with your qualifications and the role's requirements.

Advance Cancer Care Through Research and Innovation

At Shenandoah Oncology, our Clinical Research Team plays a critical role in bringing cutting-edge cancer treatments and therapies to our patients. We're seeking a detail-oriented, compassionate, and highly organized Clinical Research Coordinator to help manage clinical trials and support patients throughout their research journey.

This is an excellent opportunity for someone who is passionate about patient care, scientific advancement, and making a meaningful impact behind the scenes. The ideal candidate thrives in a fast-paced healthcare environment, values accuracy and compliance, and enjoys building strong relationships with patients, providers, and research partners.

Why Shenandoah Oncology?

At Shenandoah Oncology, you'll join a mission-driven organization where every team member plays an important role in supporting exceptional patient care. Guided by The RETIC Way — Respect, Excellence, Teamwork, Integrity, and Compassion —we foster a culture where employees are valued, supported, and empowered to grow.

Enjoy the best of both worlds: a close-knit, community-based practice culture backed by the resources, stability, and professional growth opportunities of The US Oncology Network.

Responsibilities

Screens potential participants for protocol eligibility.

Presents trial concepts and details to participants, participates in the informed consent process, and enrolls participants into clinical trials.

Coordinates participant care in compliance with protocol requirements.

May disburse investigational product and maintain accountability records.

Oversees preparation of orders by providers to ensure protocol compliance.

Packages and ships laboratory specimens to central vendors as applicable.

Completion of Hazmat and/or IATA training may be required.

In collaboration with providers, reviews participants for changes in condition, adverse events, concomitant medications, protocol compliance, and response to study treatment.

Thoroughly document all findings and participate in data collection.

Prepares study‑related documentation, including protocol worksheets, adverse event reports, institutional review board (IRB) documents, and annual continuing review reports.

Maintains regulatory documents in accordance with organizational SOPs and applicable regulations.

May assist with scheduling monitoring and auditing visits and interact with monitors/auditors as needed.

May collaborate with research leadership in study selection processes.

Participates in required training and education programs.

May contribute to education of clinical staff regarding research procedures.

Works with staff to develop action plans and improvement initiatives to enhance quality.

May compile and report protocol activity, enrollment trends, data entry compliance, and research financial information to practice leadership and providers.

May review protocol‑specific billing guides and submit billing information to the appropriate personnel.

Other duties as assigned.

Qualifications

Associate's degree in a clinical or scientific discipline required, or an equivalent combination of education, clinical research experience, and applicable certification. Bachelor's degree preferred.

Minimum three years of Clinical Research Coordinator experience in a clinical research setting required. Oncology clinical research experience strongly preferred.

Demonstrated experience independently obtaining informed consent, coordinating participant visits, managing regulatory documentation, reporting adverse events, and supporting sponsor monitoring visits preferred.

SoCRA (CCRP) or ACRP certification preferred.

Environment

Traditional office and clinical environment. The work environment characteristics described here represent those an employee may encounter while performing essential job functions. Reasonable accommodation will be provided as needed. Exposure to communicable diseases, toxic substances, medical preparations, and other conditions common to a clinical research environment.

Physical Requirements

Significant amount of computer‑based work required. Requires standing and walking for extended periods. Occasionally lift and carry items up to 40 lbs. Requires corrected vision and hearing within normal range. Reasonable accommodation will be provided to enable individuals with disabilities to perform essential functions.

Screens potential participants for protocol eligibility.

Presents trial concepts and details to participants, participates in the informed consent process, and enrolls participants into clinical trials.

Coordinates participant care in compliance with protocol requirements.

May disburse investigational product and maintain accountability records.

Oversees preparation of orders by providers to ensure protocol compliance.

Packages and ships laboratory specimens to central vendors as applicable.

Completion of Hazmat and/or IATA training may be required.

In collaboration with providers, reviews participants for changes in condition, adverse events, concomitant medications, protocol compliance, and response to study treatment.

Thoroughly document all findings and participate in data collection.

Prepares study‑related documentation, including protocol worksheets, adverse event reports, institutional review board (IRB) documents, and annual continuing review reports.

Maintains regulatory documents in accordance with organizational SOPs and applicable regulations.

May assist with scheduling monitoring and auditing visits and interact with monitors/auditors as needed.

May collaborate with research leadership in study selection processes.

Participates in required training and education programs.

May contribute to education of clinical staff regarding research procedures.

Works with staff to develop action plans and improvement initiatives to enhance quality.

May compile and report protocol activity, enrollment trends, data entry compliance, and research financial information to practice leadership and providers.

May review protocol‑specific billing guides and submit billing information to the appropriate personnel.

Other duties as assigned.

Associate's degree in a clinical or scientific discipline required, or an equivalent combination of education, clinical research experience, and applicable certification. Bachelor's degree preferred.

Minimum three years of Clinical Research Coordinator experience in a clinical research setting required. Oncology clinical research experience strongly preferred.

Demonstrated experience independently obtaining informed consent, coordinating participant visits, managing regulatory documentation, reporting adverse events, and supporting sponsor monitoring visits preferred.

SoCRA (CCRP) or ACRP certification preferred.

Environment

Traditional office and clinical environment. The work environment characteristics described here represent those an employee may encounter while performing essential job functions. Reasonable accommodation will be provided as needed. Exposure to communicable diseases, toxic substances, medical preparations, and other conditions common to a clinical research environment.

Physical Requirements

Significant amount of computer‑based work required. Requires standing and walking for extended periods. Occasionally lift and carry items up to 40 lbs. Requires corrected vision and hearing within normal range. Reasonable accommodation will be provided to enable individuals with disabilities to perform essential functions.