- IQVIA (Durham, NC)
- …in lieu of degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and ... managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences… more
- United Therapeutics (Research Triangle Park, NC)
- … clinical trial material (CTM) is available for sites and/or Contract Research Organizations (CRO); Lead final clinical study report writing to summarize ... this role you will need** Minimum Requirements + For Senior ( Clinical ) Product Development Scientist level: +... clinical development with a PhD/PharmD + For ( Clinical ) Product Development Associate Director level: +… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …efforts to support CMC Development projects. **Note: This is located in Research Triangle Park R&D laboratory.** **ESSENTIAL DUTIES and RESPONSIBILITIES include the ... in a team environment. **Occupational Demands:** Work is performed in a clinical and/or a laboratory environment. Exposure to biological fluids with potential… more
- IQVIA (Durham, NC)
- …and work in the recruiting country IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life ... and includes qualitative (eg interviews, focus groups), quantitative (eg clinical outcome assessments (COAs)/patient-reported outcomes (PROS), preference research… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …statistical software) * Works with internal teams (eg, marketing, managed markets, clinical development) to support outomes research , quality of life, and ... abstracts, posters, and manuscripts from conducted studies * The Senior Manager of Global HEOR will design, develop, oversee...Research (HEOR) in support of existing and new clinical applications in coordination with Global and US: Commercial,… more
- Actalent (Durham, NC)
- Job Description The Senior Clinical Trial Associate (Sr. CTA) is responsible for supporting the daily workflow of clinical operations activities. The Sr. ... TMF is helpful. Essential Skills + Working knowledge of ICH/GCP and clinical research processes. + Solid working knowledge and experience utilizing an eTMF… more
- IQVIA (Durham, NC)
- …as lead writer for individual summary documents. Has a broad understanding of clinical research processes and global regulatory document standards. Mentors less ... The Associate Director, Principal Medical Writer is responsible for...issue resolution). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- IQVIA (Durham, NC)
- …programming, and data management aspects of the pharmaceutical, biotechnology, device, and/or clinical research service industries. + Good working knowledge of ... Understanding of GCP, ICH, and FDA guidelines and regulations applicable to conduct clinical research . + Experience with the management and statistical analysis… more
- IQVIA (Durham, NC)
- …or equivalent experience/training preferred IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to ... ** Associate Director, IQVIA Participant Payments (ADIPP)** The ...trained, and objectives are met. The ADIPP works with senior leadership in formulating effective goals and objectives for… more