- 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 ... Officer, serve as the Subject Matter Expert (SME) and leader for Vitalief's clinical trial budgeting and coverage analysis outsourcing services. + Design,… more
- Parexel (Trenton, NJ)
- The Senior Clinical Research Associate ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... Clinical Practices (GCP), and the Sponsor's standards. The Sr . CRA is accountable for site management and monitoring,...the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:**… more
- Parexel (Trenton, NJ)
- **Job Purpose:** The Senior Clinical Research Associate ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned ... associated with the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring Responsibilities and Study… more
- IQVIA (Parsippany, NJ)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within...activities to bring revenue forward in partnership with the senior project leader. + Identify changes in scope and… more
- Merck (Rahway, NJ)
- …Atherosclerosis, Cardiology Clinical Research, Cardiovascular Diseases, Clinical Development, Clinical Studies, Clinical Trial Designs, Clinical ... **Job Description** The Senior Director ( Sr . Principal Scientist) has...medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Job Summary** Under the direction of the Director/ Associate Director of Clinical Management, the Senior Clinical Study Manager is responsible for the ... communication of any variances in budget forecast to the Director/ Associate Director. * Establish communication flow with CRO and...(s), as assigned. * Participates in ongoing review of clinical trial data focusing on data integrity,… more
- Bristol Myers Squibb (Madison, NJ)
- …projects + Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects + ... from study start to database lock. **Position Summary** The Senior Manager, Clinical Data Management is a...BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, … more
- Cardinal Health (Trenton, NJ)
- …Review agreements in support of various business transactions, including strategic sourcing, clinical trial services, confidentiality, Business Associate and ... other departments + Work under the general supervision of senior attorneys and exercise sound judgment as to matters...matters that require attention of Legal and Compliance Departments' senior leadership + Promote and ensure compliance with the… 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 (Madison, 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