- IQVIA (Overland Park, KS)
- …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 (Overland Park, KS)
- …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 (Overland Park, KS)
- …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 (Overland Park, KS)
- **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 (Overland Park, KS)
- **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 (Overland Park, KS)
- …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
- IQVIA (Overland Park, KS)
- Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ... ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking...from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- US Tech Solutions (Kansas City, MO)
- **Job Description:** + The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical ... to the development of new processes, procedures, tools and training to enhance clinical research activities and is accountable for adhering to quality standards.… more
- Eurofins (Lenexa, KS)
- …food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in ... forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global...favorably and in accordance with established Company standards and associate attributes at all times. + Other duties as… more
- Eurofins (Lenexa, KS)
- …food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in ... forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global...favorably and in accordance with established Company standards and associate attributes at all times. + Other duties as… more