Posted in Other 4 days ago.
University Overview
The 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.
The Sr. Clinical Trials Project Manager position works within the Center for Cellular Immunotherapies Clinical Operations Team. The primary mission of the Clinical Operations Team is to manage and optimize the clinical research infrastructure necessary for bringing these novel/personalized cell and gene therapies to patients. The key objectives of the Clinical Operations Team include:
Supporting the translation of first-in-human investigational cell and gene therapy products from the bench to bedside.
Managing/accelerating the clinical trial development and new study activation pathways.
Establishing internal and external collaborative partnerships.
Establishing/maintaining the infrastructure required to standardize and optimize clinical trial development and execution; and ensuring ongoing oversight/compliance.
Developing/refining standardized processes, procedures, and templates/tools to align with the changing regulatory landscape and new scientific innovation.
Ensuring the generation of high-quality, reliable and statistically sound clinical data that can be used for reporting, publication, endpoint analysis and further product development.
Identifying/implementing new technology/systems required to enhance clinical research operations.
In this role, the Sr Clinical Trial Project Manager will independently manage a portfolio of Phase I Penn-Sponsored clinical research studies. The Sr. Clinical Project Manager is responsible for the overall execution and management of their assigned projects, from initial study start-up to study close/database lock.
Core functional responsibilities of the Sr. Clinical Trials Project Manager position include:
Overall Project Planning and Implementation:
Monitor project status/timelines; Ensure all required milestones are met and that the project remains on schedule.
Provide input/expertise on core study documents.
Develop/maintain required study manuals
Manage and execute all study start-up activities; Includes coordinating/hosting the site initiation visit (SIV)
Establish/maintain the Sponsor Trial Master File (TMF)
DSMB Coordination/Management- includes development/maintenance of all required DSMB documentation, adherence to the DSMB Charter, organization/scheduling/hosting of the DSMB meeting, DSMB reporting, etc.
Qualification/oversight of 3rd party sponsor vendors (as applicable)
Work collaboratively with the Data Management team to develop a compliant study database and supportive data management documentation; PM focus on content expertise, study application, and end-user experience.
Site/Study Management
Provide seamless oversight of ongoing study activities; Support site management activities
Facilitate required updates/reporting to sponsor teams and 3rd party collaborators; Ensure adherence to data sharing/reporting requirements in contractual agreements
Support sponsor regulatory reporting requirements
Work collaboratively with the monitoring team to manage/address compliance concerns, execute training, triage exception requests/deviation reports, etc.
Develop/facilitate additional training activities including training on amendments to core study documents
Perform ongoing data management review; Ensure site adherence with data entry timelines/expectations and overall data quality/completeness
Work collaboratively with the Data Management team to plan/execute database amendments
Support data review/reporting for analysis, presentation, publications, etc.
Departmental/Team Responsibilities:
Contribute expertise/knowledge to the development/maintenance of project management policies/procedures, templates/tools, etc.
Support training/mentoring of new Clinical Operations team members
Other duties as assigned
Given the fast-pace nature of this role and the complexity of the research, eligible candidates must possess/demonstrate the following competencies:
Ability to manage projects independently
Strong analytical and problem-solving skills
Excellent organizational and time management skills
High attention to detail; demonstrated ability to multi-task
Excellent oral and written communication skills
This candidate must also have a thorough knowledge of Federal Regulations and ICH-GCP guidelines, and a comprehensive understanding of clinical trial processes, and the conduct of clinical studies.
Reference Information: The salary range included in the job posting encompasses the full range of employees at the University of Pennsylvania, with varying levels/years of experience, seniority, functional responsibilities, etc. Therefore it cannot be used as a precise indicator of the salary range for this position. The actual salary offered for this position will be determined by the Compensation Office in the Division of Human Resources and will be evaluated based on the qualifications of each individual candidate and internal equity.
Job Location: Hybrid Eligible- This position is eligible for a hybrid work schedule with a work week divided between working onsite and working remotely.
Qualifications
This position is contingent upon grant funding.
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