- Eurofins (Edison, NJ)
- …to guidelines and carry out any other duties assigned by the department manager . Position is full-time Monday - Friday 11am-7pm. Overtime as required during our ... damage or violated hold times to maintain sample integrity. + Interact with Project Managers and clients appropriately and professionally. + Follow directions or use… more
- Merck (Rahway, NJ)
- …and collaboration skills. + Experience in managing end-to-end programs and product development lifecycles. + Independent, proactive, and visionary manager with ... and data teams during the ideation phase, managing requirements, overseeing development deliverables with core technology groups, and ensuring alignment with… more
- Taiho Oncology (Princeton, NJ)
- …evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower ... maintenance, and close-out. The SA I helps with the coordination of project activities, including corresponding with internal and external team members globally,… more
- Astrix Technology (NJ)
- …+ Clinical Research Associates/Clinical Research Coordinators + Clinical Trial Managers + Clinical Project Manager + Site Start Up Specialists + Clinical Data ... and we deliver top talent to companies focused in: Pharmaceutical , Biotechnology, Diagnostics, Medical Devices, Food & Beverage, Nutraceutical,...Manager + Clinical Development Associates + SAS… more
- IQVIA (Morristown, NJ)
- …with customers including end users, licensed clinicians, IT, informatics team, EHR Manager and analyst to ensure patient safety gaps are identified as it ... group or team at leadership level, or similar role within a pharmaceutical company. + Certifications highly recommended, including: CAHIMS, CHTS, CHISP , CPHIMS… more
- IQVIA (Parsippany, NJ)
- IQVIA is seeking a highly skilled Trial Delivery Manager /Senior Clinical Lead to oversee and coordinate clinical trial management activities for both internally ... Pharmacy). + 6 or more years of clinical trial management experience in the pharmaceutical industry or large CRO. + Strong working knowledge of ICH-GCP, local laws,… more
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