- IQVIA (Parsippany, NJ)
- …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 (Parsippany, NJ)
- **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 (Parsippany, NJ)
- **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 (Parsippany, NJ)
- …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
- Gilead Sciences, Inc. (Parsippany, NJ)
- …trials, across all therapeutic areas, around the world. In partnership with Clinical Research , Medical Affairs and Development Operations functions, ensures that ... field with 4+ years of trial management experience **PREFERRED:** + Extensive clinical research knowledge and cross-functional understanding of clinical … more