- 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
- IQVIA (Kansas City, MO)
- …or equivalent education and experience + At least 1 year of experience in a clinical research setting preferred + Working knowledge of clinical trials and ... in informed consent processes + Support the safety of research subjects + Comply with company and Sponsor...#LI-HCP #ONSITE IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- Lilly (Kansas City, MO)
- …health sciences (eg BSN, RPh, PA, NP) considered if 5 or more years clinical , research or industry experience (medical or scientific role) in relevant ... to make life better for people around the world. Associate Director, Dermatology Medical Science Liaison - Kansas City...Medical Science Liaison - Kansas City Purpose: Scientific and Clinical Experts (SEs/CEs) are individuals who are noted for… more