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About the Role
Clinical research only works when patients are supported, protocols are followed, and data is collected with care. In this role, you’ll be at the center of that effort—helping patients safely participate in clinical research while ensuring each study is conducted with integrity and compassion.
As a Clinical Research Coordinator, you’ll coordinate and manage the day‑to‑day care of patients enrolled in research studies. Working closely with physicians, nurses, and research teams, you’ll help bring promising new cancer treatments from idea to reality.
This role is a great fit for someone who enjoys working directly with patients, values organization and accuracy, and wants to be part of meaningful, mission‑driven research.
What You’ll Do
You’ll support clinical research studies from a patient‑focused, operational perspective.
Your responsibilities will include:
Coordinating and managing patient care for clinical research studies
Educating patients and families about study participation and compliance
Serving as a trusted point of contact for patients throughout the study
Working closely with physicians, nurses, and research staff to support study goals
Collecting complete, accurate clinical research data
Ensuring studies follow approved protocols and regulatory requirements
Supporting patient enrollment and retention in research studies
Escalating concerns and questions with guidance from preceptors, educators, or leadership
What You’ll Bring
You’ll succeed in this role if you are compassionate, detail‑oriented, and comfortable balancing patient care with research responsibilities.
Required Certification (one of the following):
Current certification from the Association of Clinical Research Professionals (ACRP)
Current certification from the Society of Clinical Research Associates (SOCRA)
Another research‑related certification recognized by Roswell Park Comprehensive Cancer Center
Required Education and Experience (one of the following):
Bachelor’s degree and 1 year of clinical research, healthcare, or related experience
Associate’s degree and 2 years of related experience, including completion of a Clinical Research Coordinator traineeship at Roswell Park
Associate’s degree and 3 years of related experience
High school diploma or equivalent and 4 years of related experience, including completion of a Roswell Park clinical research traineeship
High school diploma or equivalent and 5 years of related experience
Certifications must be obtained and maintained within five years of appointment as a condition of continued employment. Degrees must be from an accredited or Roswell Park‑recognized institution.
Preferred Qualifications
While not required, experience in the following areas will help you stand out:
Clinical research at an academic medical center
Clinical oncology experience
ACRP or SOCRA certification
Bachelor’s degree in life sciences or a medical field
Familiarity with FDA regulations and GCP/ICH guidelines
Completed CITI training
Experience with Serious Adverse Event (SAE) and Unanticipated Problem (UP) reporting
Why You’ll Love Working Here
At Roswell Park Comprehensive Cancer Center, everything we do is focused on improving the lives of people facing cancer.
Here’s what you’ll find here:
Purpose‑driven work that directly supports cancer research and patient care
A collaborative care and research environment where your voice matters
Ongoing learning and professional development opportunities
The chance to work alongside dedicated clinicians and researchers
A comprehensive benefits package designed to support your health, career, and well‑being
Salary:
The salary range for this position is $77,264 – $95,529 annually, which includes a geographic differential and comprehensive benefits package. Final compensation will be based on qualifications, skills, and experience.
If you’re passionate about patient care, research excellence, and making a real impact in cancer treatment, we encourage you to apply.
