- 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)
- **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)
- **Position Summary** The Clinical Research Associate (CRA) will be responsible for designing, planning, coordinating, and conducting all activities involved ... Skills and Knowledge Requirements** + ≥2 years of experience as a Clinical Research Associate , with specific in vitro diagnostics study experience +… 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
- Allucent (Cary, NC)
- …life-changing therapies to patients in need across the globe. We are looking for a Sr. Clinical Research Associate (sCRA I) to join our A-team (remote, with ... and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in… more
- United Therapeutics (Raleigh, NC)
- …+ 8+ years of relevant pharmaceutical industry experience + 5+ years of direct clinical research associate experience + Working knowledge and understanding ... related field or + Registered Nurse (RN) nursing qualifications or relevant clinical research experience in pharmaceutical/biotech/medical device or CRO industry… 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
- Institute for Medical Research (Durham, NC)
- Institute for Medical Research at the Durham VA Health Care System ADMINISTRATIVE ASSISTANT PI: Dr. Stephen Freedland The Institute for Medical Research (IMR), ... Dr. Stephen Freedland, and his associates at his urology and oncology research lab. The Administrative Assistant works under the direction of the Administrative… more