- Bristol Myers Squibb (Princeton, NJ)
- …drives the development and implementation of innovative strategies and technologies for clinical trial programming. Associate Director develop collaborative ... the development and implementation of innovative strategies and technologies for clinical trial programming + Independently develops, validates, troubleshoots,… more
- Merck (North Wales, PA)
- …**Position Description:** ** Associate Principal Scientist, Statistical Programming** The Associate Principal Scientist, Clinical Trial Analysis and ... or MS plus minimum 7 years SAS programming experience in a clinical trial environment + Experience leading large and/or complex statistical programming projects… 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
- Merck (North Wales, PA)
- **Job Description** The Associate Vice President (AVP)/Section Head, Global Clinical Development, Ophthalmology will focus on driving strategy, development, and ... for clinical programs. + Supervises development of clinical documents including development plans, protocols, trial ...of clinical documents including development plans, protocols, trial related documents, clinical study reports and… more
- WuXi AppTec (Plainsboro, NJ)
- **Overview** The Clinical Research Associate III Senior Oncology performs and coordinates aspects of field-based and office-based monitoring and data quality ... specified by project manager or supervisor, including but not limited to mentoring of Clinical Research Associate (CRA) I and II personnel. + Participates in… more
- IQVIA (Abington, 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
- Merck (North Wales, PA)
- … Safety Statistics + Interact with Safety Physicians, Safety Scientists, Clinical Trial Physicians , Regulatory, Early/Late Development Statistics, Statistical ... management skills. + Good understanding of worldwide regulatory requirements and clinical trial expertise . + Strong oral and written communication skills. Able… more
- Bristol Myers Squibb (Princeton, NJ)
- …strong working knowledge of Pharmaceutical R&D business processes, particularly in Clinical Trial Operations, with demonstrated command of key concepts, ... enable Global Development Operations (GDO) function, specifically focusing on Veeva Clinical Vault (Veeva CTMS, Veeva eTMF). This role owns end-to-end responsibility… more
- Bristol Myers Squibb (Princeton, NJ)
- …team of outsourcing managers within a specific therapeutic area(s) and manages clinical trial vendor partnerships that supports alliance and outsourcing ... management across multiple service categories of clinical trial activities in R&D. **Key Responsibilities**...R&D. **Key Responsibilities** + Leads a team of Outsourcing Associate Directors and Managers within a specific therapy area,… more
- Bristol Myers Squibb (Princeton, NJ)
- …more: careers.bms.com/working-with-us . Global Data Management (GDM) is responsible for clinical trial data acquisition, data standards governance, data ... 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
- 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...representative of those that must be met by an associate to successfully perform the essential functions of this… 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
- Bristol Myers Squibb (Princeton, NJ)
- …This includes a centralized triage function for informed consent negotiations with global clinical trial sites, IRBs/ECs, and health authorities, as well as ... internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to...Simplification. + Knowledge of IT systems used to support clinical trial processes and the authoring of… more
- Bristol Myers Squibb (Princeton, NJ)
- …leads the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning, ... treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director, Biostatistics is a core member of cross-functional development teams and… more
- Merck (North Wales, PA)
- …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. MS in Computer Science, Statistics, Applied Mathematics, ... plus 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** + Excellent interpersonal skills… more
- Virtua Health (Marlton, NJ)
- …which may include quality improvement data and tracking information submitted to clinical trial sponsors and regulatory agencies. Coordinates visits for ... Additional Locations: Job Information: Job Summary: Coordinates and participates in clinical research studies conducted by principal investigators. Acts as a liaison… more
- Virtua Health (Marlton, NJ)
- …as required by protocol to ensure the submission of accurate information to clinical trial sponsors and regulatory agencies.* Responsible for submitting all ... *This is not a remote position* Summary:Coordinates and participates in clinical research studies conducted by principal investigators. Acts as a liaison… more
- Merck (North Wales, PA)
- …minimum of 9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. + MS (preferred) in Computer Science, Statistics, ... minimum of 7 years Statistical Analysis System (SAS) programming experience in a clinical trial environment. **Required Experience and Skills:** + Proven track… more
- Bristol Myers Squibb (Princeton, NJ)
- …the Quality Module for regulatory submissions to support biologics products regarding: Clinical trial applications; New marketing applications; HA responses & ... current regulatory requirements and expectation for small molecule arketing applications, clinical trial applications for projects, and/or lifecycle changes to… more