- 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 ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Durham, NC)
- …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in… more
- IQVIA (Durham, NC)
- **Job Overview** Join our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to ... all protocols, regulations, and sponsor requirements. **Essential Functions** + **Site Monitoring:** Conduct selection,...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- IQVIA (Durham, NC)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… 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 ... company experience in clinical development with a PhD/PharmD + For ( Clinical ) Product Development Associate Director level: + Master's degree or +… more
- Actalent (Durham, NC)
- Job Title: Research Proposal Associate II Job Description We are seeking a dedicated and experienced Research Proposal Associate II to join our team. ... role involves the development and revision of proposals for various research studies, including those initiated by investigators, industry, government, and… more
- UNC Health Care (Raleigh, NC)
- …laboratory procurement and information services department. 6. Attend Investigator and Clinical Research Coordinator meetings for various upcoming protocols. ... **Licensure/Certification Requirements:** **Professional Experience Requirements:** * Previous experience in clinical or laboratory research field preferred. **Knowledge/Skills/and… more
- IQVIA (Durham, NC)
- …OVERVIEW** IQVIA Site Enablement Solutions (SES) is a unique service providing site-based clinical research staff to trial sites globally. Reporting to the ... and development of new SES services. In addition, this Associate Director role will be a key contributor to...Typically requires a minimum of 7 years of prior clinical research experience, with preference given to… more
- ThermoFisher Scientific (Morrisville, NC)
- …associated with the applicants training (comparable to 2 years). + Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company ... **Environmental Conditions** Office **Job Description** **Overview:** Provides medical oversight of clinical trials to ensure company SOPs, client directives, good … more