Cra jobs in Kansas

 ...coordination with Senior Clinical Project Managers, the Head of the Fluorescence Imaging Clinical Team, and other team members. The Sr CRA will also travel frequently to Investigational Sites to conduct co-monitoring along with the assigned Field CRA(s)/Monitor(s)... 

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile... 

A leading biotech firm in Overland Park is hiring a Clinical Research Associate I (CRA I) to support clinical studies through site monitoring and management. The CRA I is responsible for ensuring compliance with protocols and regulations, conducting various monitoring visits... 

A reputable medical institution in Kansas City is seeking a Clinical Research Assistant to support clinical trials in the Division of Pulmonary, Critical Care, and Sleep Medicine. Ideal candidates will have experience in health sciences or related fields, along with strong...

A leading health data science company is seeking a Clinical Research Associate (CRA) to manage monitoring and site management tasks. Candidates should have 1-2 years of onsite experience, particularly in Cardiovascular, Oncology, or Neurology. The role involves regulatory... 

IQVIA LLC is seeking a Clinical Research Associate to conduct site monitoring visits, manage study progress, and ensure compliance with regulations. Qualified candidates should have a Bachelor’s Degree in a scientific discipline or healthcare and at least 1.5 years of on...

A leading clinical research provider in the United States is seeking a Study Start-Up Clinical Research Associate. This role includes responsibility for site selections and the execution of study-specific start-up activities for Phase I-IV trials. The ideal candidate will...

A global healthcare firm is seeking a Study Start-Up Clinical Research Associate in Overland Park, KS. This role is responsible for site selections and start-up activities for Phase I-IV trials. Candidates should have at least 6 months of experience in on-site or in-house...

IQVIA is hiring a Senior Clinical Research Associate in Overland Park, Kansas. The role involves conducting site visits, managing compliance, and supporting trial execution. Candidates should have a Bachelor’s degree in life sciences and at least 1.5 years of on-site monitoring...

Job Overview: Join our dynamic team as a Clinical Research Associate! Youll 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 cancer...

 ...regulations, Good Clinical Practice, and study-specific requirements. Review visit reports and manage any issues brought to their attention by CRA staff and/or the study team and/or Sponsor. Oversee Corrective Actions/ Preventive Actions (CAPAs) of assigned staff to ensure timely... 

 ...project site budgets and regulatory filings that aligns with SOPs, study guidelines and GCP best practices. In the function of Lead CRA, will act as primary liaison between CRAs and project team and may be required to participate in the development of project plans, protocols... 

IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic, Oncology, and/or Neurology. Candidates can be located anywhere in the US. Job Overview... 

 ...States of Americatime type: Full timeposted on: Posted Todayjob requisition id: R1537623IQVIA is hiring Clinical Research Associates (CRA) at the CRA 2 level. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/... 

 ...6 months of on-site or in-house monitoring experience. Candidates can be located anywhere in the United States. The Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I‑IV trials... 

 ...materials: National Council of University Research Administrators (NCURA) Pre-Award Certificate, Certified Research Administrator (CRA), Grant Professional Certification (GPA), or other nationally recognized professional certification related to grant proposal... 

Overview The Clinical Research Assistant (CRA) in the Division of Pulmonary, Critical Care, and Sleep Medicine supports clinical trials by assisting with various aspects of research, including participant recruitment, data collection, and compliance with regulatory guidelines... 

 ...you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate (CRA) to join our diverse and dynamic team. As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial... 

 ...other professional customer service qualities to maximize the most out of the client relationships. Moderate understanding of HMDA, CRA Community Development, and CRA Small Business Revenue inputs to ensure proper reporting and compliance for the bank. Solid... 

 ...Parexel FSP is looking for a CRA/Sr CRA in the US. Oncology Experience required. Cell therapy experience is strongly preferred. Job Purpose: The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is...