- Parexel (Trenton, NJ)
- …in Lupus is preferred -Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability ... experience treating rheumatology patients clinically and/or who possess extensive rheumatology clinical trial related experience will be considered for this… more
- 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
- Bausch + Lomb (Trenton, NJ)
- …ensuring alignment with global requirements. + Provide guidance on risk assessment, clinical trial design implications, and regulatory pathways. + Support ... regulatory strategies for development programs and marketed products across CMC and clinical /non- clinical , labeling, adpromo areas. Serve as a strategic advisor… more
- Bristol Myers Squibb (Princeton, NJ)
- …effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback loop to ... adjusted when new or unanticipated issues arise once the trial has begun. **Key Responsibilities:** + Develop the Quality...with the CAPA CoE and Serious Breach pillar and Clinical Quality Assurance to gather input from audits, inspections,… 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
- Norstella (Trenton, NJ)
- …& analytics **Requirements** + Deep knowledge and expertise of the pharma strategic Clinical trial landscape (Clin Dev/Ops, clinical development plan ... industry suppliers, advisors, and investors. Our clients are generally senior -level decision makers in need of support to ensure...+ Experience using data analytics and services to solve clinical trial challenges + Understanding of how,… 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
