Senior Clinical Research Coordinator Salary at Perelman School Of Medicine University Of Pennsylvania BETA

Position Senior Manager/Associate Director, Clinical Operations The Senior Manager / Associate Director, Clinical Operations will report directly to the VP of Clinical Operations and will independently oversee clinical studies from concept to close-out. The ideal candidate will ensure all clinical trial activities are performed in accordance with applicable SOPs, company policies, and regulatory guidelines. The primary focus of this role is to provide high-touch oversight to CROs and other 3rd party vendors to ensure study milestones are achieved and high-quality clinical data are delivered in a timely manner to support Context’s drug development program. Company Context Therapeutics, Inc. Responsibilities Job Responsibilities include, but are not limited to: Oversee operational aspects of assigned clinical trial(s) and oversees clinical trial conduct including study start-up, enrollment, maintenance and close-out Ensure adherence to agreed budgets and timelines Communicate with functi

Job Summary We are seeking a dedicated and detail-oriented Senior Scientific Program Administrator to oversee the administration and coordination of selected AACR task forces and related scientific initiatives. The ideal candidate will have a background in lung cancer and will work closely with the chair(s), subject matter experts, VP, and AACR leadership to ensure that operations are well managed and aligned with the organization's goals. The Senior Scientific Program Administrator will be supported by a Program Associate who will assist with administrative tasks. While taking direction from the chair, AACR leadership, and experts, the candidate will report to the VP in this role. Responsibilities Task Force Management: Collaborate with the chair(s), subject matter experts, VP, and AACR leadership to manage AACR task forces, ensuring that task force activities, communications, and deliverables are well coordinated. Work with the VP to make decisions that support the task force's objec

Barrington James is proud to partner with an innovative and rapidly growing organization to recruit a Senior Clinical Research Coordinator (CRC) for their flagship site in Princeton, NJ. This role offers an exciting opportunity to work in a state-of-the-art facility with eight treatment rooms, contributing to groundbreaking oncology and radiopharmaceutical research. The ideal candidate will bring extensive experience in oncology clinical research and a strong background in academic or site network settings. This is a pivotal position for professionals looking to shape the future of oncology and urology treatments. Key Responsibilities: Coordinate and oversee clinical trials with a primary focus on oncology and urology studies. Manage all aspects of patient recruitment, informed consent, and retention while ensuring patient safety and compliance with study protocols. Collaborate with investigators, sponsors, CROs, and internal teams to maintain trial quality and compliance. Ensure accur

Job Description Job Description Our ideal candidate will be a "go-getter" with prior experience in the healthcare field and will: · Bachelor’s or Associate degree in marketing /business administration · Be creative, entrepreneurial, and a strategic thinker. · Be self-motivated with strong time-management skills. · Have experience with Area Agency on Ageing, hospitals and long-term care facilities. · Possess excellent oral and written communication skills · Be comfortable meeting with clients both at home and in clinical settings, such as hospitals, nursing facilities as well as with Service coordinators and social workers Primary Responsibilities · Call on and develop relationships with physicians, hospital discharge planners, skilled nursing facilities, home health and hospice agencies, assisted living communities, adult day care centres, senior community centres, and a variety of community-based organizations. · Coordinate post-discharge home care with hospital and skilled nursing fa

Job Description Job Description Working under the direction of the Senior Director, Clinical Research, the Senior Project Manager (SPM) will be responsible for the overall management of all projects including liaising between the funder and the project team for oncology clinical trials managed by the organization. The Senior Project Manager coordinates the efforts of all project teams to ensure that all aspects of all projects as defined in the contract are occurring on schedule and within budget. Job Responsibilities Assists the Sr. Director in all aspects of clinical trial management Reviews contract, protocol, budget and Case Report Forms (CRF's) in the development of the scope of the project Coordinates and oversees the development of project teams including members of Medical, Data Management, Regulatory, Monitoring, and Clinical Supplies departments as needed Oversees the development and implementation of the project plan Assures that all project tasks are performed per SOPs and