In-house Clinical Research Associate II - Oncology - U.S. Remote

Worldwide Clinical Trials

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About The Position

In-House CRAs play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. These roles help drive breakthrough scientific research and play a lead role in every clinical trial. At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.

Requirements

• Bachelor’s Degree or a Nursing Degree required.
• Minimum of two years experience as an In-House CRA or four years as a Clinical Research Coordinator (CRC) required.
• Experience in Oncology trials required.
• High level of proficiency in both spoken and written English required.

Nice To Haves

• Excellent interpersonal, oral, and written communication skills in English.
• Ability to contribute to a team remotely.
• Strong customer focus, ability to interact professionally within a sponsor contact.
• Proficiency in Microsoft Office, CTMS, and EDC Systems.

Responsibilities

• Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
• Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.).
• Provide applicable updates for site related documentation for filing in the Trial Master File (TMF).
• Perform feasibility studies/site identification activities for potential sites, as requested.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Bachelor's degree