Posted in Other 7 days ago.
University OverviewThe University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn's distinctive interdisciplinary approach to scholarship and learning. As an employer Penn has been ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America's Best Large Employers in 2023.Penn offers a unique working environment within the city of Philadelphia. The University is situated on a beautiful urban campus, with easy access to a range of educational, cultural, and recreational activities. With its historical significance and landmarks, lively cultural offerings, and wide variety of atmospheres, Philadelphia is the perfect place to call home for work and play.The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more.
Posted Job TitleResearch Project Manager A (OBGYN - Ovarian Cancer Research Center)
Job Profile TitleManager Research Project A
Job Description SummaryThe OCRC Tumor Bio-Trust Collection is a GMP/GLP laboratory and service center in the Ovarian Cancer Research Center. The Research Project Manager (RPM) A reports to the Technical Director and is responsible for the entire life cycle of the specimens, starting from identifying potential patients, procurement in cooperation with HUP, PAH, and CCH surgical teams, to aseptic processing, through banking and inventory management, to retrieval and disbursement. All work is done independently with minimal supervision. Work schedule can be irregular which may require early arrival, evenings, weekends, and potentially holidays. The Research Project Manager maintains meticulous auditable records, in a HIPPA compliant manner, of all specimens collected so they can be linked back to the original donor or de-identified as appropriate. The RPM aids in regulatory compliance by tracking informed consents and writing and revising SOPs. RPM also assists in the writing and editing of informed consent forms (ICF). RPM is responsible for a majority of obtaining informed consent from patients which includes explaining the study, discussing risks and benefits, and answering any questions. Specimens include but are not limited to human blood, and solid and liquid tumor tissue. Processing skills include dissection, tissue sampling and prep, blood handling and gradient purification, and advanced cell culture techniques for working with primary cells. The RPM is responsible for monitoring and maintaining all laboratory equipment, supplies, and space, as well as creating requisitions for lab supplies. RPM is constantly improving work processes to meet the increased demands of the study. Such processes include working with Information Services from the health system to create an electronic version of the consent in PennChart. The RPM liaises with cooperative entities including clinicians from Gynecologic Oncology, Medical Oncology, and Pathology, clinical and translational research teams, staff at other facilities such as TTAB, Penn BioBank, and the Pathology Clinical Service Center, as well as facilities staff such as the building administrator. As a service center, the RPM is also responsible for communicating and assisting the consumers, both internal and external, to determine appropriate sample types identify the specimens they need and then fulfilling their requests. The Rapid Autopsy Program has many moving parts and requires coordination between the patient and their care team, the anatomic pathology department, the research team, and any necessary transportation. The RPM is an integral player by being the center of coordination and execution for all these moving parts. Recruitment to enroll participants in the program requires establishing good rapport with the patient and their family. The RPM must be comfortable having candid but delicate conversations about end of life. The program is also expanding to multiple disease sites; the Specialist is responsible for acting as an ambassador of the program, as such, it has been extended to the Pancreatic Cancer Research Center. In addition to banking and enrollment responsibilities, the RPM collaborates on research projects with some of the internal PIs. RPM also provides processing support for clinical trials as well as project management support, such as directing specimens to be processed for analysis. RPM also provides lab training and support for clinical research staff. RPM also regularly attends research seminars and training opportunities.
Job Description
Job Responsibilities
The Research Project Manager A (RPM A) position is specifically for the Tumor BioTrust Collection at the Ovarian Cancer Research Center (OCRC). The RPM A will be primarily responsible for managing various research projects and implementing various research study protocols while developing and managing work plans and timeframes in order to meet the project goals. The RPM will be maintaining and managing contacts with various entities including our external collaborators, commercial partnerships, as well as various vendors we closely work with. In addition, the RPM A will be performing the essential daily responsibilities starting from identifying potential patients and obtaining consent for tumor banking purposes, procurement in coordination with HUP, PAH, and CCH surgical teams, to aseptic processing, through banking and inventory management, to retrieval and disbursement. They will play a pivotal role in supporting seamless operations and expansion of the PSOM-approved service center as well as supporting internal and external investigators' biospecimen needs and research. The RPM will assist in assuring regulatory compliance by writing and editing of the IRB protocol, informed consent forms (ICF) as well as creating an electronic version of the consent form in PennChart. The RPM will also play an essential role in successful coordination and execution of the Penn Legacy Tissue Program (PLTP, aka Rapid Autopsy Program) and the program is also expanding to multiple disease sites including the Pancreatic Cancer Research Center. The RPM will be acting as an ambassador of the program ensuring the successful execution of the RAP. We are back filling the previous RPM (Dalia Omran) and are seeking to hire an RPM with skills sets essential to this work and who's devoted and equipped to performing a higher level of complexity and supervisory role.
*Position is contingent upon funding*
Qualifications
We are seeking to hire an RPM with skills sets essential to this work and who's devoted and equipped to performing a higher level of complexity and supervisory role. Prior experience with Redcap, LabVantage, and human biospecimens is required. The ideal candidate will have strong computational skills and be proficient with computer-based systems including but not limited to Word, Excel, Redcap, iLab, and other online database programs. The ability to work independently with strong problem-solving skills is necessary. Strong interpersonal skills and clear communication with the clinical research team, directors and primary investigators is required.
Salary offers are made based on the candidate's qualifications, experience, skills, and education as they directly relate to the requirements of the position, as well as internal and market factors and
the pay range assigned to the job profile.
Audacy |
Audacy |
Audacy |