- Amicus Therapeutics (Princeton, NJ)
- …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 ... day-to-day activities associated with clinical trial operations. The Senior Associate Clinical Trial Manager is responsible for assisting the… more
- Bristol Myers Squibb (Princeton, NJ)
- …projects + Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects + ... we pioneer. Join us and make a difference. The Senior Manager, Clinical Data Management (Data Management...BMS R&D pipeline. This role reports to the Director, Clinical Data Management or Associate Director, … more
- Merck (Trenton, NJ)
- …to:** + Collaborate closely with biomarker scientists and project teams to plan clinical trial biomarker set-up using logistical strategies to ensure efficient ... **Job Description** We are currently seeking a Senior Scientist within the Integrated Biomarker Operations organization...and Skills:** + Drug discovery experience, including familiarity with clinical trial execution in Oncology studies. +… more
- Bristol Myers Squibb (Princeton, NJ)
- …of smart systems and optimal approaches to support the end to end clinical trial data lifecycle, from collection through submission. + Holding accountability ... in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, Clinical Data Standards is a...**Experience Requirements** + At least 12 years of global clinical trial expertise and a successful track… more
- Bristol Myers Squibb (Princeton, NJ)
- …clear product vision and strategy for the clinical data ecosystem especially with clinical trial design and data science methodologies to enable clinical ... team! **Position Summary:** We are seeking a highly motivated and detail-oriented Associate Director - Product Manager with broad clinical data experience… more
- Edwards Lifesciences (Trenton, NJ)
- …the requirements of the Associate Manager Required + Experience in clinical trial design, indication lead + FDA/EMEA/PMDA submission experience + The ... us and be part of our inspiring journey. As ** Senior Manager, Biostatistics, TMTT** , you will use your...+ Act as core team member/lead biostatistician of assigned clinical trial (s) in US and international/global … more
- Bristol Myers Squibb (Princeton, NJ)
- …. **Position Summary** Global Data Management (GDM) is responsible for clinical trial data acquisition, data standards governance, data management, ... trials across the BMS Research & Development portfolio. The Associate Director, External Data Acquisition is a leadership role...Acquisition is a leadership role with oversight of external clinical trial data acquisition and integration and… more
- Bristol Myers Squibb (Princeton, NJ)
- …Include : + Conduct risk assessments specific to medical affairs and clinical trial /research activities, utilizing a combination of data analytics, ... d raft simple, easy to understand policies specific to medical affairs and clinical trial /research activities that empower the business to execute activities in… more
- Astrix Technology (Trenton, NJ)
- …space. + Working knowledge of Clinical & Regulatory systems such as Clinical Trial Management System (CTMS), electronic Trial Master Files (eTMF), ... for the sale and growth of Astrix Technology Group's Clinical and Regulatory Consulting services to a portfolio of...of success in new significant client development, selling to senior IT and line of business executives, managers, and… more
- Merck (North Wales, PA)
- …optimal trial design and monitoring of studies, producing high-quality clinical documents and presentations. The position requires a solid understanding of the ... **Job Description** The Associate Vice President (AVP)/ Metabolism Section Head in...development of assets within the Metabolism Section of Global Clinical Development + May serve as a senior… more
- Novo Nordisk (Plainsboro, NJ)
- …experience with Supplier Management, Research Administration, Grant Operations, Grant Management, clinical trial management, or a similar research operations ... a difference? The Position Reporting to the head of Clinical , medical, Regulatory (CMR) Business Operations, the Associate...GCP Principles and the application of those principles to trial design, planning & conduct of clinical … 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 ... Senior Scientific Director Translational Medicine (TM), the TM Associate Director will be part of the late stage...group. The individual will be responsible for TM and clinical biomarker activities to support drug development programs in… 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 will be… more
- Bristol Myers Squibb (Princeton, NJ)
- …across a matrix. * Experience with drug development, commercialization, and healthcare, clinical trial management a plus. **\#LI-Hybrid** If you come across ... (WWMA) Cell Therapy (CT) Organization. **Details** This role reports directly into the Senior Director of Strategy and Operations and will be a strategic and… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …experience in pharmacovigilance + In depth knowledge and experience of clinical trial methodology, pharmacovigilance regulations, signal detection and ... to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director, Signal Management Process Excellence in Cambridge, MA, where you will… more
- Merck (North Wales, PA)
- …support for anticipated promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates to the ... **Job Description** Reports to the Director/ Senior Director in the Office of Promotion and...the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for the review and approval… more
- Novo Nordisk (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… more
- Novo Nordisk (Plainsboro, NJ)
- …(phase I trials) + Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol, Clinical Trial Report, Investigator's Brochure (IB), ... the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future,...within the US East Coast Development Hub comprised of Senior Global Safety Leads, Global Safety Leads and … more