- Vitalief (New Brunswick, NJ)
- …seeking a dynamic, strategic, and client-facing leader to build and lead our Clinical Trial Budgeting and Coverage Analysis Services. This role combines hands-on ... serve as the Subject Matter Expert (SME) and leader for Vitalief's clinical trial budgeting and coverage analysis outsourcing services. + Design, launch, and… more
- Sumitomo Pharma (Trenton, NJ)
- …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that… more
- Parexel (Trenton, NJ)
- …associated with the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring Responsibilities and Study ... **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
- Taiho Oncology (Princeton, NJ)
- …sciences is preferred. Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site management experience in the pharmaceutical, ... team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for operational study support...to multi-task and effectively prioritize in order to ensure clinical trial goals. + Recognize potential obstacles… more
- Parexel (Trenton, NJ)
- …activities associated with the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:** + Ensure proper ... The Senior Clinical Research Associate (Sr. CRA) is...quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites… more
- System One (Basking Ridge, NJ)
- Job Title: Clinical Study Associate I Location: Basking Ridge, NJ Type: Contract - 1 year Contractor Work Model: Hybrid - must be able to go onsite 1-4 ... the life sciences industry? Joule is currently seeking a Clinical Study Associate to join an industry-leading...This is a high-visibility role where your expertise in Trial Master File (TMF) integrity will directly support the… more
- Bristol Myers Squibb (Princeton, NJ)
- … development, the position is responsible for various aspects of ongoing clinical trial program-related activities within the relevant therapeutic area. These ... their personal lives. Read more: careers.bms.com/working-with-us . **Summary** The Associate Director of Clinical Science plays a...may be assigned. + Acquires and utilizes knowledge of clinical trial design to develop or oversee… more
- Sumitomo Pharma (Trenton, NJ)
- …clinical research program with minimal direction + Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing ... seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The … more
- Bristol Myers Squibb (Princeton, NJ)
- …your application should be directed to Chat with Ripley. R1597891 : Associate Director, Oncology Clinical Biomarker Asset Lead, Translational Development ... will offer the greatest possible benefit to patients. **Position Summary** The Clinical Biomarker Asset Lead role will be responsible for development and execution… more
- Mallinckrodt Pharmaceuticals (Bridgewater, NJ)
- …policies. Research & Development Support: + Provide legal counsel on clinical trial agreements, investigator-initiated studies, and collaborations with academic ... Job Title Associate General Counsel, Advertising & Promotion / Clinical Development Requisition JR000015569 Associate General Counsel, Advertising &… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …of assigned trial (s), as assigned. * Participates in ongoing review of clinical trial data focusing on data integrity, trending and consistency. * Supports ... **Job Summary** Under the direction of the Director/ Associate Director of Clinical Management, the...Word, Excel, PowerPoint, Outlook, etc.) * Good understanding of clinical trial related software (eg, eCRFs, IRT,… 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 + ... BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, ...functional study team members to ensure on-going review of trial data currency, quality and completeness + Represents DM… more
- ThermoFisher Scientific (Bridgewater, NJ)
- …patient recruitment strategies and the implementation of digital and decentralized clinical trial solutions. + Proven experience providing protocol review ... of Patient-First technology solutions, supporting future innovation and advancing patient-centric clinical trial methodologies. At Thermo Fisher Scientific, we… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …As core study/project team member, provide statistical input in different perspective of the clinical trial conduct such as CRF review, IRT setting, DMC set up, ... products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of... clinical , statistical, and regulatory literature for current clinical trial results, regulatory trends and new… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . Job Description The Associate Director, RBQM - HOCT, ICN will mainly be responsible for ... effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback loop to… more
- System One (Princeton, NJ)
- …RAVE). + Lead data reporting and BI efforts, including graphical dashboards to support clinical trial progress and operational KPIs + Ensure compliance with CFR ... Job Title: Associate Director of IT - Life Sciences/ Clinical...technical staff and non-technical business stakeholders + Familiar with clinical systems and trial platforms such as… more
- J&J Family of Companies (Titusville, NJ)
- …more at https://www.jnj.com **Job Function:** R&D Operations **Job Sub** **Function:** Clinical Trial Project Management **Job Category:** Professional **All Job ... directed to your accommodation resource. **Required Skills:** **Preferred Skills:** Budgeting, Clinical Trial Designs, Clinical Trials, Compliance… more
- Novo Nordisk (Plainsboro, NJ)
- …launch), ensuring plans support successful launch readiness and long-term access + Shape clinical trial design and build business cases by providing pricing, ... to launch). This role shapes market access and pricing assumptions, informs trial design and business decisions (eg device strategy, indication sequencing), and… more
- Sumitomo Pharma (Trenton, NJ)
- …regulatory submissions and working with regulatory templates + Understanding of EU Clinical Trial Regulation and ROW country regulatory requirements related to ... a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part… more
- Bristol Myers Squibb (Princeton, NJ)
- … Overview for Type II variation and coordinate expert reports. + Provide clinical trial expertise for existing evidence generation studies or health-authority ... Read more: careers.bms.com/working-with-us . **Position Summary:** The Established Brands Associate Director, Medical Affairs, is responsible for leading and… more