- Pfizer (Collegeville, PA)
- …way in healthcare and make a lasting impact on society.** **What You Will Achieve** As a Clinical Study Team Lead (CSTL), you will be an integral member ... team delivery of multiple complex global studies and/or programs. Your clinical development expertise...operations + Accountable for issue escalation and resolution + Lead study team chartering and… more
- University of Pennsylvania (Philadelphia, PA)
- …Response website (https://coronavirus.upenn.edu/) for the latest information. Posted Job Title Clinical Research Coordinator B/C ( BioBank Research Studies ) Job ... Coordinator needed to assist research teams in recruitment and study implementation for Penn funded research studies ....flyers, managing participant data via RedCap and Excel.. The Clinical Research Coordinator C will also establish study… more
- Pfizer (Collegeville, PA)
- …etc.), and lead translation of pre- clinical observations into clinical experiments and studies designed to demonstrate proof of pharmacology, proof ... **ROLE SUMMARY** The Clinical Lead (CL), Internal Medicine RU...of clinical research plans into efficiently delivered studies . Creative in the conception of novel study… more
- Abbott (Philadelphia, PA)
- … clinical sites and other Abbott clinical staff (eg, operations management, study team , Site Contracts Associate), as needed. **Manage all aspects of ... female executives, and scientists. **The Opportunity** The **Associate Clinical Site Lead ** for the Philadelphia, PA region drives study execution and… more
- CSL Behring (King Of Prussia, PA)
- …biotherapies used to treat serious and often rare conditions. Could you be our next Lead Clinical Oversight Manager? The job is located in the King of Prussia ... the processes (eg eTMF) and standards to allow inspection readiness of all clinical studies and ensuring compliance with quality standards. Manage internal… more
- CSL Behring (King Of Prussia, PA)
- …develop the operational strategy for a clinical studies and a clinical prgrams and the end-to-end study delivery of all operational activities and budget ... Trial Leaders. **Responsibilities:** Plan and build one or more clinical studies /programs: ** Lead the SET...EC/ IRB and regulatory submissions** **Ensure internal and external study team members are trained on the… more
- University of Pennsylvania (Philadelphia, PA)
- …They will also engage in compliance monitoring and data management with other study team members including the data analyst and biostatistician. The CRC ... psoriasis participating in research; among other health disparities related studies . The primary responsibility of the Clinical ...manage basic to moderately complex databases (eg REDCap). + Lead development of CRFs by reviewing study … more
- University of Pennsylvania (Philadelphia, PA)
- …They will also engage in compliance monitoring and data management with other study team members including the data analyst and biostatistician. The ideal ... psoriasis participating in research; among other health disparities related studies . The primary responsibility of the Clinical ...study CRFs. + Coordinate efforts and feedback between study team for complex database development. +… more
- University of Pennsylvania (Philadelphia, PA)
- …to protocol and in accordance with Good Clinical Practice, detailed documentation of study activities. + Act in lead capacity in coordination of ACC CRU ... levels; share study -wide updates/issues with the Research Team 's Program Manager and study team...with physicians to assist with design, set-up and execute studies . Be responsible for writing investigator-initiated IND/IDE clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …as protocols and consents, lead team meetings, and may take a lead role in study communication with internal and external groups. Work directly with ... Work with Regulatory Specialist for regulatory submissions. Communicate with study team members. Recruit, consent, and screen...investigators to design, set-up and execute studies . Accountable for making sure study timelines… more
- University of Pennsylvania (Philadelphia, PA)
- …and assist maintaining lab equipment as needed. + Participate in reoccurring study team meetings and ongoing protocol training; facilitate and participating ... IND, and GCP guidelines by all personnel involved in clinical studies . + Assist in the preparation...relevant bodies, and may supervise other lab members in clinical study -related activities. Effective problem-solving abilities; effective… more
- University of Pennsylvania (Philadelphia, PA)
- …A Job Description Summary To assist the research team in recruitment and study implementation for two (2) funded studies (RESPECT3 Penn Biobank ROR and the ... evaluate and analyze clinical data. Responsible to assist with study coordination and recruitment for investigator-initiated studies , multi-center research … more
- University of Pennsylvania (Philadelphia, PA)
- …programs within the ACC. The Myeloma Research Team seeks a full-time, registered Clinical Research Nurse (CRN) to conduct studies involving a wide variety of ... various sponsors. This position will report directly to the Lead Clinical Research Nurse and work directly... Team Leaders and Principal Investigators with initiating study procedures for new IITs and industry-sponsored clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …to protocol and in accordance with Good Clinical Practice, detailed documentation of study activities. + Act in lead capacity in coordination of ACC CRU ... partnering institutions and creates multi-center budgets and manages expenses. Participates in study team meetings, disease site group meetings, and ongoing… more
- University of Pennsylvania (Philadelphia, PA)
- …as protocols and consents, lead team meetings, and may take a lead role in study communication with internal and external groups. Work directly with ... in initiation, monitoring, audit and close-out visits. Participate in study team meetings and ongoing protocol training/compliance...Description The Coordinator B will participate in and coordinate clinical trials and clinical studies … more
- University of Pennsylvania (Philadelphia, PA)
- …with Research Team Leaders and Principal Investigators with initiating study procedures for new IITs and industry-sponsored clinical trials. Manage ... of the University of Pennsylvania seeks a full-time, registered Clinical Research Nurse C/D to conduct studies ...plan of care in collaboration with the PI and study team and in accordance with research… more
- University of Pennsylvania (Philadelphia, PA)
- …as protocols and consents, lead team meetings, and may take a lead role in study communication with internal and external groups. Work directly with ... and diagnostics. Coordinator duties include: Assist in development of study documents. Communicate with study team...investigators to design, set-up and execute studies . Accountable for making sure study timelines… more
- University of Pennsylvania (Philadelphia, PA)
- …in accordance with the specific clinical protocol as approved by the Sponsor, study team and in accordance with all regulatory organizations. S/he will play ... study protocols. The Project Manager will manage/supervise the study teams assuring that each clinical trial...Project Manager will provide oversight and support for each study team , lead team… more
- Pfizer (Collegeville, PA)
- … Lead (and members of the development team ) to establish, lead , coordinate, and execute the early oncology clinical development plan(s) for one ... signals of efficacy (ESOE) and proof of concept (POC) studies . + *The OES Clinical Scientist (Senior...protocol and may participate as an individual contributor on clinical study teams and clinical … more
- University of Pennsylvania (Philadelphia, PA)
- …ability to implement and execute higher level studies . May take a lead role in study communication with internal and external groups. Works directly ... PCAM and PPMC. The coordinator will actively participate in study team meetings, ongoing protocol training, and...+ Support and manage the coordination of Phase I-IV clinical trials + Coordinate and organize study … more