Lead Oncology CRA: Site Management & Study Startups

Catalyst Clinical Research, LLC

North Carolina

Hybrid

USD 900,000 - 1,100,000

Full time

14 days+

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Job summary

Worldwide Clinical Trials is seeking a seasoned Clinical Research Associate (CRA) based in the United States with Oncology experience. You will oversee research activities at sites, participate in all study stages, start-up activities, contracts, data collection training, and safety reporting, while maintaining regulatory compliance across sites.

You will join a global CRO focusing on high-quality clinical trials across multiple therapeutic areas.

Qualifications

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.

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, start-up activities, contracts and budgets, training sites to collect data, and reporting safety events.
Manage site's activities during study maintenance and close-out when the study ends.
Conduct study initiation visits (SIVs) and ensure regulatory compliance across sites.