Senior Clinical Research Associate - Oncology - Central U.S. - Remote
What you will do
- Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
- Typically involved in reputed company stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of reputed company and budgets, training the sites to collect data properly and report any potential safety-reputed company events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded
- Conduct study initiation visits (SIVs)
- While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-reputed company events, and adhering to reputed company applicable regulatory requirements
What you will bring to the role
- Excellent interpersonal, oral, and written communication skills in English
- Superior organizational skills with attention to detail
- Ability to work with little or no supervision
- Proficiency in reputed company Office, CTMS, and reputed company Systems
Your experience
- 5+ years of experience as a Clinical Research Associate
- 4-year university
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