Senior Clinical Research Associate - Oncology - Central - Remote
About The Position
Worldwide Clinical Trials is a global, midsize CRO dedicated to pushing boundaries and innovating in the pursuit of cures for persistent diseases. We are a team of over 3,500+ experts committed to changing the way the world experiences CROs and improving lives through our work. Our Clinical Operations team offers a rewarding journey where contributions profoundly impact patient lives. As a Clinical Research Associate (CRA), you will collaborate with brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. We foster a supportive and team-oriented environment, providing extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Regular touchpoints and coaching conversations with your Line Manager ensure professional development is a top priority, with a clear career path that can lead to Clinical Trial Manager roles. Our accessible Executive Leadership team is committed to advancing science and overcoming obstacles to improve patient lives. We offer an unparalleled experience where you can drive scientific breakthroughs and be at the core of every successful clinical trial.
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 in the Central United States.
- 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.
- 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 depending on location.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
