Data Coordinator – Trauma, Burn, and Injury Prevention
Children's Mercy Kansas City
Senior Clinical Research Associate – CNS
Worldwide Clinical Trials
full-time
Posted on:
Origin: • 🇺🇸 United States
Visit company websiteJob Level
Senior
About the role
- Manage research activities at sites participating in Worldwide’s clinical research projects (predominantly registries and other non-interventional/observational studies).
- Involved in all stages of the clinical study including site identification and study start-up activities.
- Collect appropriate regulatory documents and support negotiation of contracts and budgets.
- Train sites to collect data properly and report potential safety-related events.
- Manage site activities during study maintenance and close down research activities at study conclusion.
- Conduct study initiation visits (SIVs).
- Perform most site management remotely while ensuring compliance with informed consent, safety reporting, and regulatory requirements.
Requirements
- Excellent interpersonal, oral, and written communication skills in English.
- Superior organizational skills with attention to details.
- Ability to work with little or no supervision.
- Proficiency in Microsoft Office, CTMS and EDC Systems.
- 5+ years of experience as a Clinical Research Associate.
- 4-year university degree or RN/BSN in Nursing.
- Experience in CNS required; experience in Psychiatry strongly preferred.
- Candidates must reside in the Central United States.
- Willingness to travel required.
