Jeffersonhealth

Clinical Research Project Manager

Philadelphia, PA · Part-time

Sponsorship not specified$40k-$50kDetected 1 day ago

GCPProject ManagementAuditingHRISClinical TrialsClinical ResearchPatient CareResearchLeadershipCommunicationGxP

About the role

This role provides operational oversight of research activities, including feasibility planning, subject recruitment and retention, data and specimen management, and regulatory compliance.
Additionally, the position represents the organization in internal and external forums and serves as a subject matter expert, providing strategic guidance and consultation at the departmental or institutional level.

The Clinical Research Project Manager independently leads and manages clinical trials from study start-up through closeout, ensuring adherence to protocol requirements, institutional standards, and applicable regulatory guidelines.
The manager may supervise and develop research staff, drives process improvements, and contributes to the development of standard operating procedures.
Prepares, reviews, and submits regulatory and IRB documentation in a timely manner, maintains accurate study records and subject logs, tracks study finances, and performs quality control assessments to ensure integrity, accuracy, and audit readiness of clinical trial data.
Leads or supports research operations within a division or department, contributes to and implements standard operating procedures, participates in leadership initiatives, and represents the organization internally and externally while providing expert consultation on clinical research processes and compliance.

Bachelor's Degree
5 years clinical research experience and
3 years clinical research experience and
Patient transporters can walk 8-10 miles per shift. *Patient care providers may be required to perform activities specific to their role including kneeling, bending, squatting and performing CPR.

Oversees the completion of all necessary regulatory preparations prior to sponsor visits (e.g., monitoring and auditing visits, site activation visits).
and tracking quality metricsDirects regulatory documentation and workflow for clinical trials through the use of project management techniques and tools (e.g., spreadsheets, progress reports, priority setting).

Colleagues have access to tuition discounts at Thomas Jefferson University after one year of full time service or two years of part time service.
All colleagues, including those who work less than part-time (including per diem colleagues, adjunct faculty, and Jeff Temps ), have access to medical (including prescription) insurance.
For more benefits information, please click here

Oversees the completion of all necessary regulatory preparations prior to sponsor visits (e

This listing is sourced directly from Jeffersonhealth's careers page and normalized into a canonical job model.