- IQVIA (Parsippany, NJ)
- …and owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are ... to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery,… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …practices and processes to achieve objectives. + Exhibit strong problem-solving, analytical, and project management skills. + Thrive in a matrix environment with ... The Associate Director, External Data Services, plays a critical...and industry best practices. This position collaborates closely with Clinical Data Management teams and External Data… more
- Merck (Rahway, NJ)
- … Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and ... Principal Scientist can also be responsible for several effectiveness studies within a project , participating as the clinical representative in project teams… more
- Sanofi Group (Morristown, NJ)
- …to do advanced statistical analyses using SAS or R. + Demonstrated strong project management , interpersonal and communication skills. + Exhibited expertise to ... **Job Title:** Statistical Project Leader ( Associate Director) **Location:** Morristown,...and Decision Science (EGDS) group** at Sanofi unites Biostatistics, Clinical Statistical Modeling, and Real-World Evidence to revolutionize data-driven… more
- Parexel (Trenton, NJ)
- …patients we serve. Parexel's defined Biotech Division offers opportunities for seasoned Project Management professionals with a strong background running global ... minimum, 2+ years' experience leading Global Clinal Trials in Project Management within a CRO (preferred), Biotech...be required for the more senior roles of Senior Project Leader, Associate Project Director,… more
- Parexel (Trenton, NJ)
- …Clinical Research Associate (Sr. CRA) is responsible for the site management , site monitoring and close-out of assigned clinical trials investigator sites ... documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management , study progress and metrics + Identify… more
- Sumitomo Pharma (Trenton, NJ)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The ... associate medical director is responsible for the leadership, development, and management of clinical studies while building and maintaining relationships… more
- Parexel (Trenton, NJ)
- …Clinical Research Associate (Sr. CRA) is responsible for the site management , site monitoring and close-out of assigned clinical trials investigator sites ... documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management , study progress and metrics + Identify… 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, ... and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more
- IQVIA (Parsippany, NJ)
- …per site basis. * If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according ... Job Overview Perform monitoring and site management work to ensure that sites are conducting...contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)… more