- Parexel (Raleigh, NC)
- … clinical trials. Performs other duties as necessary to ensure optimal clinical trial execution. **Key Accountabilities** **:** **Study Team Support** + ... has an exciting opportunity for a Senior Precision Medicine Associate . This role works closely with line Manager, Precision...collection procedures and presentation slides) + Manages acquisition of clinical trial samples + Provides support for… more
- ThermoFisher Scientific (Greenville, NC)
- …and non-promotional materials to ensure global compliance. + Manages global Clinical Trial Authorization (CTA) submissions and strategy, aligning labeling ... Supply Chain to ensure accurate and timely implementation of labeling decisions. + ** Clinical Trial Regulatory Responsibilities** + Develop and oversee global … more
- Sumitomo Pharma (Raleigh, NC)
- …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
- ThermoFisher Scientific (Greenville, NC)
- …and financial planning processes in response to significant business growth. The Associate Manager will lead key initiatives across financial planning, ... our Global Central Labs (GCL) group, where we support clinical research in over 100 countries with ground breaking...over 100 countries with ground breaking lab and digital trial services. We're growing fast, and we're looking for… more
- ThermoFisher Scientific (Greenville, NC)
- …organization and time management skills Preferred Skills & Abilities: + Clinical trial , contract research organization (CRO), pharmaceutical, biotechnology, ... **Environmental Conditions** Office **Job Description** We are recruiting for an Associate Director, Global Market Development to support the PPD FSP solutions… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …+ Ensure regulatory intelligence specialists have continued access to regulatory, clinical trial , and public domain information resources to identify ... The Associate Director of Regulatory Intelligence leads the collection...may impact pharmaceutical practices, procedures and controlled documents. + Lead weekly regulatory intelligence team meetings to include review… more
- Veterans Affairs, Veterans Health Administration (Garner, NC)
- …other personnel and provides indirect support to the Chief Technologist and Lead Technologists. Position includes general management of patient flow, quality of ... as assigned under the direction of a supervisor or lead . Work Schedule: 0730-4:00 M-F & 8:00-4:30 M-F Requirements...will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness… more
- Veterans Affairs, Veterans Health Administration (Garner, NC)
- …RME are responsible for knowing what designated RME is used in their clinical area and following the local Standard Operating Procedure (SOP) drafted in accordance ... will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness...the incumbent [can operate independently] and has demonstrated specific clinical competency in the appropriate specialty and taken and… more
- University of North Carolina- Chapel Hill (Chapel Hill, NC)
- …methodological leadership, especially in designing, implementing, and evaluating clinical trials and other complex research projects. Key Responsibilities: ... advanced research design methods 2. Methodological Leadership & Consultation * Partner with Associate Dean for Research to consult with faculty and students to plan… more