- Parexel (Trenton, NJ)
- **Job Summary:** Core member of the Clinical Trial Team (CTT), independently managing all vendor-related aspects of global clinical trial (s) to deliver ... + Very strong vendor management skills; outsourcing, contracting, and sourcing of clinical trial services + Results-driven: demonstrated ability of completing… more
- Parexel (Trenton, NJ)
- …quality + Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to ... & North Carolina The Senior Clinical Research Associate (Sr. CRA) is responsible for the site...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- Parexel (Trenton, NJ)
- …information to create investigator/institution entities within the CTMS system to then enable site association with a clinical trial ; routinely reconciles ... Parexel FSP has an exciting opportunity in Site Start Up! The Associate Manager,...Trial Master File; Captures relevant study, country and site level information and milestones within the CTMS system… more
- 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
- 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
- IQVIA (Parsippany, NJ)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/ Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures...activities from start-up to close-out. + Escalate and resolve trial issues and contribute to CAPA processes. ** Site… more
- IQVIA (Parsippany, NJ)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... inspection readiness, and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within a role that is… more
- Taiho Oncology (Princeton, NJ)
- …biological sciences is preferred. Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site management experience in the ... 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
- Bristol Myers Squibb (Princeton, NJ)
- …15+ years of demonstrable experience in pharmaceutical industry with proven expertise in clinical trial execution, data acquisition, and analysis reporting on a ... Clinical Data Management, and related domains such as Clinical Analytics, Site Selection, Feasibility, and Real-World...data products, and analytic ready data solutions for GDD Clinical Intelligence ( Trial Simulation & Modeling, … 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
