- Merck & Co. (North Wales, PA)
- …or related field and at least 5 years SAS programming experience in a clinical trial environment orMS in Computer Science, Statistics, Applied Mathematics, Life ... position is a key collaborator with statistics and other project stakeholders in ensuring that project plans...at least 3 years SAS programming experience in a clinical trial environment. Required Skills: Effective interpersonal… more
- Merck & Co. (North Wales, PA)
- …years of experience with all of the following: SAS programming in a clinical trial environment including data steps, procedures, SAS/MACRO, and SAS/GRAPH; ... of potential medical breakthroughs.Review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … Director and Clinical Operations lead Support investigator meetings Serve on Clinical Trial Strategy Team in collaboration with Clinical Operations ... other stakeholders. The Medical Director will also assist the Senior Medical Director in the development and execution of...Medical Affairs team on relevant disease state topics and clinical trial data. Review and approve resources… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …decisions (phase I trials) Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol, Clinical Trial Report, Investigator's Brochure ... lifecycle of the actual product Responsible for all areas related to patient safety in clinical trials Act as member of the trial safety group for dose… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …decisions (phase I trials) Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol, Clinical Trial Report, Investigator's Brochure ... lifecycle of the actual product Responsible for all areas related to patient safety in clinical trials Act as member of the trial safety group for dose… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D ... across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as… more
- University of Pennsylvania (Philadelphia, PA)
- …technology/systems required to enhance clinical research operations. In this role, the Sr Clinical Trial Project Manager will independently manage ... of health and wellness programs and resources, and much more. Posted Job Title Sr . Clinical Trial Project Manager (Center for Cellular Immunotherapy) Job… more
- J&J Family of Companies (Titusville, NJ)
- …LLC (6084) **Relocation Eligible:** No **Travel** Yes, 25 % of the Time **Job Function** Clinical Trial Project Management **Req ID:** 2406201295W ... Sr . Director, Engagement - 2406201295W **Description** **Johnson &...impact to participant health and wellbeing by reinventing the clinical trial experience. The Innovative Health Engagement… more
- Pfizer (Collegeville, PA)
- …Therapeutic Areas. Your project management skills will be leveraged to develop clinical trial timelines and oversee budgets for the assigned clinical ... Medicine, Anti-Infectives, or Inflammation & Immunology preferred. + Broad experience in a Clinical Trial Execution discipline (eg senior study management… more
- Amicus Therapeutics (Princeton, NJ)
- Senior Associate, Clinical Trial Manager (Contractor) Location Princeton, NJ Requisition ID 2292 # of openings 1 Apply Now ... (https://phh.tbe.taleo.net/phh04/ats/careers/v2/applyRequisition?org=AMICUS&cws=37&rid=1338) Senior Associate Clinical Trial Manager (Contractor) Amicus… more
- CSL Behring (King Of Prussia, PA)
- **The Opportunity** The Clinical Trial Supply (CTS) Senior Study Manager manages the end-to-end supply chain for assigned clinical studies throughout the ... multi-year study lifecycle. The CTS Senior Study Manager independently leads clinical studies...to clinical sites and patients. + Develop clinical trial supply documents and training to… more
- Taiho Oncology (Princeton, NJ)
- …Biostatistics, PV, PK, Biomarkers and Medical Writing etc.), to deliver high quality clinical trial results. + Use scientific expertise to support the creation ... Sr . Manager, Clinical Research Scientist Pleasanton,...of cancer treatment and improving patients' lives. As a Senior Manager, Clinical Research Scientist, you will… more
- Bristol Myers Squibb (Princeton, NJ)
- …of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with ... clinical studies and programs. This position involves leading and executing clinical trial activities, collaborating with cross-functional teams, and liaising… more
- Bristol Myers Squibb (Princeton, NJ)
- …of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with ... the conduct + May serve as Clinical Trial Lead for one or more...Intermediate medical writing skills and medical terminology + Basic planning/ project management skills (develop short range plans that are… more
- Bristol Myers Squibb (Princeton, NJ)
- …molecular assays and generation of research use genomics data in support of BMS clinical trial analysis. This includes but is not limited to responsibility for ... execution of biomarker analysis for BMS translational medicine and clinical programs. The Sr . Scientist candidate must...develop and execute the qualification/validation of these assays for clinical trial assays in house and/or potentially… more
- Bristol Myers Squibb (Princeton, NJ)
- …stage drug development + Experience in activities required for and related to clinical trial initiation, maintenance and completion + Experience in interacting ... we pioneer. Join us and make a difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr . Principal Scientist… more
- Bristol Myers Squibb (Princeton, NJ)
- …in late stage drug development and activities required for and related to clinical trial initiation, maintenance and completion + Strong verbal and written ... successful candidate will have prior therapeutic area and late development clinical experience in biotech/pharma organizations interacting with project teams,… more
- IQVIA (Philadelphia, PA)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines *… more
- Lilly (Philadelphia, PA)
- …Operations) in the planning and execution of a manufacturing strategy to meet clinical trial supply requirements. + Manage the creation of, and lifecycle, ... organizations (CMO) globally to ensure reliable and sufficient supply to Avid/Lilly clinical trials. + Develop, implement, and execute upon supply chain strategy for… 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 ... but are not limited to:** + Participates as a key stakeholder on the Clinical Trial Teams (CTT) and collaborates closely with other functional area… more
