Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects.
Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort.
Perform various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets.
Train the sites to collect data properly and report any potential safety-related events.
Manage the site's activities during study maintenance, and close down research activities at the sites once the study has concluded.
Conduct study initiation visits (SIVs).
Requirements
5+ years of experience as a Clinical Research Associate
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
4-year university degree or RN/BSN in Nursing
Experience in Acute Schizophrenia is required
Inpatient experience strongly preferred
Candidates must reside in the Southeast United States in close proximity to an international airport
Willingness to travel regionally required.
Benefits
We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.
Professional development opportunities.
Clear career path and development that can lead to Clinical Trial Manager roles.
Accessible Executive Leadership team committed to advancing science and making a difference.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.