Clinical Research Associate II - Oncology - United States (Remote)

Worldwide Clinical Trials•Durham, NC

2d•$79,500 - $158,500•Remote

About The Position

Worldwide Clinical Trials is a global, midsize CRO that is dedicated to finding cures for the world's most persistent diseases through pioneering and creative approaches. We are a global team of over 3,500+ experts committed to improving lives. Our Clinical Operations team works to advance clinical research and has a profound impact on patients' lives. As a Clinical Research Associate (CRA) at Worldwide, you will collaborate with brilliant minds across diverse therapeutic areas including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. We offer extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Professional development is a priority, with regular touchpoints and coaching conversations with your Line Manager, and 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 patients' lives worldwide. 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.
2 - 5 years of experience as a regional, traveling Clinical Research Associate.
4-year university degree OR Nursing Degree.
Experience in Oncology is required.
Willingness to travel regionally required.

Responsibilities

Managing the research activities at sites participating in Worldwide’s clinical research projects.
Involved in all stages of the clinical study, including identifying potential sites, performing study start-up activities (collecting regulatory documents, supporting contract and budget negotiation), training sites on data collection and safety reporting, managing site activities during study maintenance, and closing down research activities at sites upon study conclusion.
Conduct study initiation visits (SIVs).
Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements, with most site management efforts performed remotely.