- 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)
- **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
- Catalyst Clinical Research LLC (Raleigh, NC)
- As a Senior Clinical Research Associate , you...research with direct site monitoring experience with a sponsor company or CRO and 3 years of recent ... regulations including ICH/GCP and PhRMA guidelines along with Catalyst Clinical Research 's applicable SOPs and working practices....is provided to the Field Monitor from the assigned Clinical Trial Associate . + Works closely with… more
- IQVIA (Durham, NC)
- IQVIA MedTech is seeking a Clinical Research Associate II with Medical Device monitoring experience! Central Nervous System (CNS) experience is a plus! Job ... on-site monitoring experience + Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice… 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
- IQVIA (Durham, NC)
- The ** Associate Clinical Lead Director** provides leadership to the global Oncology clinical team, in support of the project leader, and in collaboration ... in a health care or other scientific discipline with 10 years clinical research /monitoring experience; or equivalent combination of education, training and… 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