Clinical Research Coordinator (Phase 1 Team)

Job Description

A large healthcare provider in Philadelphia, PA is seeking a Sr Clinical Research Coordinators to support its growing clinical research program. These are newly created positions driven by continued expansion of the research team and clinical trial portfolio.

The Clinical Research Coordinator will play a key role in the day-to-day management of oncology clinical trials, ensuring studies are conducted in compliance with protocol requirements, Good Clinical Practice (GCP) guidelines, and institutional policies. This individual will work closely with investigators, patients, sponsors, and research staff to coordinate study activities from startup through closeout.

Responsibilities include managing clinical trial operations, obtaining informed consent from study participants, coordinating patient visits, supporting orientation and training activities, overseeing central laboratory processes, maintaining study documentation, preparing for monitor visits, assisting with data collection and management, completing study reports, supporting low-risk institutional trial submissions, and tracking IRB submissions, approvals, and renewals.

This is an excellent opportunity to join a nationally recognized cancer center and contribute to cutting-edge oncology research that directly impacts patient care and treatment outcomes.

Skills and Requirements

• Experience as a coordinator working on Phase 1 clinical trials, oncology preferred, but not required.
• Hands-on experience coordinating interventional drug trials, including patient enrollment, informed consent, visit coordination, ordering protocol-required labs and imaging, and interaction with study monitors.
• Strong understanding of clinical trial protocols and the ability to execute study procedures in compliance with protocol, GCP, and regulatory requirements.
• Experience working directly with patients on clinical research drug trials.
• Excellent organizational skills with the ability to manage multiple studies and priorities in a fast-paced environment. Oncology experience Bachelors or Masters Degree

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [email protected].