- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The** **Position** The Clinical Trial Manager (CTM), Translational Medicine and Early Development (TMED) is responsible for assisting in ... vendors. The CTM will also assist to manage the clinical study team and help to coordinate meetings and...defining, monitoring and reporting on all aspects of key trial performance indicators, including for example, country and site… more
- Merck (West Point, PA)
- … **Primary activities include, but are not limited to:** - Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional area ... etc.) as well as other organizations such as Global Clinical Trial Operations (GCTO) Regional colleagues and...prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders. - Responsible… more
- Merck (West Point, PA)
- …as the GCS spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related meetings. The incumbent must ... to:** + Participates as a key stakeholder on the Clinical Trial Teams (CTT) and collaborates closely...prepares, analyses, and/or develops mitigation strategies for review with clinical partners and senior leaders. + Works… more
- Merck (Upper Gwynedd, PA)
- **Job Description** The GPAM Senior Specialist , Value & Implementation Project Manager (VIPM), is a core member of Value & Implementation (V&I) Team, partnering ... the R&D pipeline and realize its full potential. The Senior Specialist is expected to provide project...Adaptability, Adaptability, Change Management, Clinical Supplies Management, Clinical Supply Chain Management, Clinical Trial… more
- ThermoFisher Scientific (Collegeville, PA)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel… more
- University of Pennsylvania (Philadelphia, PA)
- …The Associate Director for Regulatory Affairs will facilitate ongoing improvement of clinical trial compliance and quality assurance through communication of ... with IND/IDE/Expanded Access Applications, drug development process, medical writing, and clinical trial operations required. + Qualified candidates must also… more
- Merck (North Wales, PA)
- **Job Description** **Role Summary** * The Senior Specialist , Global Medical Information is an entry-level headquarters (HQ)-based role within V&I Global Medical ... Training of internal stakeholders; and Compendia and Pathways Submissions. * The Senior Specialist has an advanced educational background and reports into… more