Neuroscience Clinical Research Project Specialist (Remote)

American College of Radiology•Philadelphia, PA

9h•$65,000 - $87,000•Remote

About The Position

The American College of Radiology (ACR) is a professional association serving over 40,000 members. The ACR’s Center for Research and Innovation (CRI) has been a world leader in radiology clinical research for over 50 years, conducting trials and projects that have transformed radiology practice, informed clinical practice standards, led to new device approvals, and changed healthcare policy. The CRI serves as the core radiology resource for NCI multicenter clinical trials involving diagnostic or therapeutic radiology. Through active research committees, the CRI has developed and delivered a diverse range of research studies in partnerships with academia and commercial sponsors, including prospective clinical trials, retrospective reader studies, clinical and imaging registries, novel imaging methods and imaging software, validation of biomarkers, radiomic feature analysis, and AI algorithm development and validation. ACR is seeking a Clinical Research Project Specialist to provide support to ACR study initiatives across the College.

Requirements

A genuine passion for advancing research in the neuroscience/neurocognitive field (e.g., Alzheimer’s research, etc.).
Practical experience with Copilot AI prompt engineering and writing, complemented by a mastery of MS Office and Smartsheet.
Proven track record in clinical research operations and customer success management.
Exceptional interpersonal skills with a knack for curating internal/external communications and managing shifting priorities.
3+ years of related experience, with a strong preference for CRO or clinical research project management backgrounds.
Solid knowledge of Good Clinical Practices (GCP) and the Code of Federal Regulations (CFR).

Nice To Haves

Bachelor’s degree preferred.

Responsibilities

Partner with research site staff to streamline and support activation, accrual, ongoing operations, and close-out activities for assigned clinical research studies.
Draft and refine essential clinical study documents, including project plans, protocols, informed consent forms (ICFs), and site facing operational resources.
Generate and manage concept documents for IRBs, imaging oversight committees, grant applications, and business proposals.
Lead protocol team operations by managing regular calls, distributing action-oriented minutes, coordinating protocol amendments, and facilitating site educational sessions.
Manage and track all assigned project deliverables, providing regular metrics and progress reports to leadership and external stakeholders.
Guarantee that all study activities and documentation strictly adhere to Good Clinical Practice (GCP) guidelines and the Code of Federal Regulations (CFR).