- 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 (Raleigh, NC)
- …according to local requirement. **MINIMUM RECRUITMENT STANDARDS:** + **2.5 years of clinical research coordination experience at site level** + Nursing or ... of education, training and experience IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… 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
- ICON Clinical Research (Raleigh, NC)
- …friendliest people in the sector, and you'll be helping shape an industry. As a Clinical Research Associate at ICON, you'll work within a large-scale, ... CRA II or Senior CRA (Single- Sponsor ) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an… 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
- Medtronic (Raleigh, NC)
- …procedures including TMVR or LAAC or other adjacent therapies + Clinical Research experience including coordinating multi-center trials and/or significant ... group presentations and hands-on experience with interventional/surgical cardiac procedures + Clinical Research experience in structural heart or other medical… 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
- IQVIA (Durham, NC)
- …_This is a remote/WFH opportunity_ IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life ... Responsible for the operational implementation of the imaging strategy for assigned clinical studies in collaboration with the Clinical Trial Team (CTT).… more