Senior Clinical Research Associate - Oncology - Midwest

About the role

As a Clinical Research Associate (CRA) at Worldwide Clinical Trials, you will work across diverse therapeutic areas including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. You'll collaborate with top-tier colleagues in a supportive, team-oriented environment with extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.

Responsibilities

• Manage research activities at sites participating in Worldwide's clinical research projects
• Participate in all stages of the clinical study, including identifying potential sites, performing study start-up activities (collecting regulatory documents, supporting contract and budget negotiations), training sites on data collection and safety reporting, managing site activities during study maintenance, and closing down research activities at study conclusion
• Conduct study initiation visits (SIVs)
• Perform remote site management while ensuring compliance with informed consent, safety event reporting, and applicable regulatory requirements

Qualifications

• 5+ years of experience as a Clinical Research Associate
• 4-year university degree OR Nursing Degree
• Current experience in Oncology required; CAR-T experience desired
• Fluent in written and verbal English required
• Willingness to travel regionally required

Skills

• 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

Pay

United States of America – $97,000.00 – $193,000.00 annually. Final salary determined based on relevant experience, performance, education, and internal equity.

Schedule

Prefer candidates residing in the Midwest with regional travel required.