- Merck (West Point, PA)
- …trials, guiding projects from late-stage preclinical work through clinical proof-of-concept studies . + **Translational study design** : Design, oversee, and ... of novel PET radiotracers from late preclinical development into first-in-human studies . This role will primarily focus on clinical implementation of novel… more
- University of Pennsylvania (Philadelphia, PA)
- …Cardio-Oncology. Responsibilities will include screening records for eligibility, recruitment of study subjects, conducting study visits, data collection and ... study team members and external departments to successfully execute studies . In addition, this position will assist with regulatory submissions. Job Description… more
- University of Pennsylvania (Philadelphia, PA)
- …A Job Description Summary Assists in the management of clinical studies under direct supervision by coordinating patient screening, enrollment, data collection, ... proposals, and presentations. Works closely with the Principal Investigator, manager, and study team to address study needs, implement approved changes, and… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …direction of the Director/Associate Director of Clinical Management, the Senior Clinical Study Manager is responsible for the oversight and management of Otsuka ... clinical studies , including coordination with other relevant parties (eg, other...to the development and review of all critical clinical study documents, including clinical protocols, informed consent forms, or… more
- University of Pennsylvania (Philadelphia, PA)
- …of Pennsylvania for ACCELERATE-PACE, LivCog, I-Spot and other supported studies (PI/Serper). These are multi-year, multi-site investigations on various observational ... through an electronic health record, patient recruitment, ensuring completion of study activities by study subjects, biospecimen collection and processing,… more
- J&J Family of Companies (Spring House, PA)
- …involves collaborating with cross-functional teams, in close partnership with Study Responsible Physicians/Clinical Leads, to design, plan, and manage complex ... protocols and materials and supports the completion of clinical study reports and regulatory filings. As a core member...to ensure timely scientific and clinical execution of clinical studies . + Maintain the quality and integrity of clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …research subjects across Penn Campus. Research coordinator work includes study implementation, community outreach, document development, regulatory work, subject ... recruitment and enrollment, study visits and regulatory... visits and regulatory compliance in one or more studies across Penn Campus Job Description Job Responsibilities Clinical… more
- IQVIA (Bethlehem, PA)
- …US based **JOB OVERVIEW** The main purpose of this role is to manage the assigned IRT studies in a way that ensures all patients get the study drug on time and ... study and data integrity are maintained from study go live to close out. An important aspect...to develop the relationship with the client while the study is ongoing in such a way that they… more
- Parexel (Harrisburg, PA)
- …clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices ... work closely with the Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the set-up, running and close-out of… more
- CSL Behring (King Of Prussia, PA)
- …the program + providing clinical oversight and expertise during development of clinical studies + serves as medical monitor for assigned clinical trials or provides ... (DT) This position is a "Lead Author" or "Contributing Author" for: + key study documents, including but not limited to the Clinical Development Plan (CDP), the… more
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