- 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. 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 (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
- Parexel (Topeka, KS)
- …Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to travel 15-20% is required _**Internal ... anticipation of future needs, we are seeking an additional Associate / Medical Director to join Parexel's highly recognized...of the projects according to contracted agreement with the sponsor (ie: tasks and time per task contracted) and… more
- IQVIA (Lenexa, KS)
- …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