Clinical Research Manager - (Community Oncology) - Southwest Region

UPMC•Cranberry Township, PA

5d•Hybrid

About The Position

UPMC Hillman Cancer Center is seeking a regular full-time Regional Clinical Research Manager to support the Community Oncology program in the Southwest greater Pittsburgh, PA region. This position will work a Hybrid daylight schedule Monday through Friday. It will have responsibility for network locations with clinical research services in Pittsburgh at UPMC Mery, Uniontown, McKeesport at UPMC McKeesport, West Mifflin, Cranberry & McCandless at the UPMC Passavant locations, Mt. Lebanon, and Washington, PA along with our Trinity location in Steubenville, OH. The Regional Clinical Research Manager is part of Hillman’s centralized Clinical Research Services (CRS) infrastructure. This position is responsible for the operational management and oversight of all clinical research activities supporting the Community Oncology program within the Southeast region. In partnership with regional physician leads, the role advances the strategic development, growth, and integration of clinical research across Hillman Network locations, ensuring clinical trial opportunities are aligned with community patient needs, disease center priorities, and Hillman’s broader research strategy. The Regional Clinical Research Manager works closely with investigators, community site leadership, and CRS teams to expand access to oncology clinical trials and advance Hillman’s mission to deliver high‑quality research closer to home. The Clinical Research Services (CRS) team is made up of nearly 200 staff members who facilitate the development, implementation, coordination, internal data monitoring, and completion of oncology-focused trials at Hillman. These trials include institutional (investigator-initiated), multi-center cooperative group/National Clinical Trial Network (NCTN), consortium, and industry-sponsored trials. Using a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data collection, and specimen collection and processing.

Requirements

Bachelor’s degree in nursing (BSN), Biomedical, or Business required.
Certification in research or clinical specialty is required.
7 years of professional experience required.
Prior supervisory/management experience is required.
5 years of clinical research experience with a preferred degree.
Must be able to demonstrate the knowledge and skills necessary to provide care and/or interact appropriately to the ages of the patients served by the department.
Must have excellent organizational skills, meet requests from multiple individuals, and respond appropriately to sudden workload changes.
Must possess excellent presentation skills and written and verbal communication skills.
Leadership abilities
Excellent role model
Knowledge of the adult learning principles
Solid/strong/good or higher on most recent performance evaluation and maintained in current practice

Nice To Haves

BSN or Master's preferred.

Responsibilities

Creates a caring and compassionate patient focused experience by building healing relationships with patients, families and colleagues.
Responsible for day-to-day operations of a complex disease center, including staff oversight, conducts recruitment and evaluation, work assignment, mentor's professional development of staff, responsible for timely activation and execution of all studies in the disease center, provides managerial oversight of smaller disease centers.
Oversees the day-to-day activities of the clinical research program and provides direct supervision to the clinical research staff.
Hires clinical research staff and has responsibility for delegating tasks, monitoring workloads, and evaluating job performance.
Serves as liaison between study sponsors and PIs; serving as the key coordinator for multi-center trials involving subject enrollment.
Demonstrates the ability to create a shared vision applies critical thinking skills and utilizes financial and quality data and conceptual knowledge in the development of the department vision and operational plan.
Demonstrates a passion for developing others, enthusiastically and expertly precepts new hires during the orientation process and serves continuously as a mentor.
Orchestrates complex change and acknowledges the psychological transition on self and others.
Takes responsibility for identifying his or her ongoing professional development needs and independently seeks resources and opportunities to meet those needs, such as through membership in nursing, oncology, or research organizations.
Develops strategies to maximize timely completion of disease center specific CRFs and data collection forms within standard of practice guidelines.
Involves stakeholders and experts in planning, designing, and redesigning change.
Disseminates new knowledge and innovations through presentations, posters, and publications.
Develops strategies to ensure protocol compliance and patient safety.
Applies critical thinking skills and utilizes quality data and conceptual knowledge in the development of the department vision and operational plan.
Creates developmental paths to increase the expertise of staff. Initiates innovation in staff development, clinical orientation, continuing education, and supports specialty certification.
Assists in institutional review board (IRB) document preparation and submission.
Monitors and facilitates completion of all protocol required data elements within CTMA and ensure all electronic data capture is complete and accurate.
Supports and assist in research coordination for high profile/high risk clinical trials.
Accountable for the recruiting, retaining, and developing of clinical research staff.