- IQVIA (Durham, NC)
- IQVIA is hiring a Clinical Research Associate with on-site monitoring experience in GLP-1/Obesity/Diabetes (Type II) clinical trials. Phase 1 experience ... degree. Req * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice (GCP) and… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …innovative medicines, solutions and services in more than 110 countries and regions. **The Clinical Research Associate assists in the management of the ... queries. Monitors and/or co-monitors as required with CRO and CRA staff to insure study integrity and compliance. Reviews...preferred. + Typically requires 2 years of experience in clinical research , including a minimum of 1… 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 ... Whether you're beginning or continuing your career as a CRA , this role is an ideal stepping-stone. You'll have...three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. +… more
- 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
- ICON Clinical Research (Raleigh, NC)
- CRA II early phase w/ healthy volunteers (home-based near... clinical development. We are currently seeking a Clinical Research Associate II to join ... our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials,… more