Senior Clinical Research Associate - Oncology - Midwest/Central
About The Position
Worldwide Clinical Trials is a global, midsize CRO that focuses on pushing boundaries and innovating to find cures for persistent diseases. We are looking for passionate individuals to join our team of over 3,500 experts who are dedicated to improving lives. Our Clinical Operations team works on diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. We foster a supportive and team-oriented environment where collaboration and creativity are encouraged. As a Clinical Research Associate (CRA), you will be an integral part of advancing clinical research, receiving extensive support through regulatory submissions, TMF management, and in-house CRAs for site management needs. We prioritize professional development through regular coaching and offer a clear career path that can lead to Clinical Trial Manager roles. Our accessible Executive Leadership team is committed to scientific advancement and overcoming obstacles to improve patient lives.
Requirements
- 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 Microsoft Office, CTMS, and EDC Systems
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree OR Nursing Degree
- Experience in Oncology is required
- Candidates must reside on the Midwest or Central Regions
- Willingness to travel regionally required
Responsibilities
- 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, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related 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)
- Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements, while most site management efforts will be performed remotely
Benefits
- Competitive benefits package
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
Associate degree
