- 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 (Charlotte, NC)
- …in lieu of degree. Req * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... 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)
- …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
- University of North Carolina- Chapel Hill (Chapel Hill, NC)
- …seeks a Research Associate to lead and support high-impact research , clinical , and community engagement initiatives in collaboration with the CARE . ... will also ensure adherence to all university, federal, and sponsor regulations governing human subjects research , data...+ Experience in HIV , infectious disease, or immunology research . + Experience in biomedical, clinical , or… more
- ThermoFisher Scientific (Wilmington, NC)
- …management and oversight of all contracted services. **Discover Impactful Work:** The Associate /Medical Director provides medical oversight of clinical trials to ... experience (comparable to 2 years)and one of the following: + Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company… more
- IQVIA (Durham, NC)
- …bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ... expectations. Your work will directly contribute to the integrity and quality of clinical research data. **Key Responsibilities** + Conduct all types of site… more
- ThermoFisher Scientific (Wilmington, NC)
- …and preparations **Skills:** + Knowledge in global regulatory and compliance requirements for clinical research , including but not limited to US CFR, EU CTD, ... (oral and written) **Experience: 6+ years' experience in pharmaceutical industry and/or clinical research organization, including 4+ years clinical study… more
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