Senior Clinical Research Associate - Oncology - Central U.S.

Worldwide Clinical Trials • Research Triangle Park, NC

1d • Remote

About The Position

Worldwide Clinical Trials is a global, midsize CRO that is dedicated to changing the way the world experiences CROs by taking pioneering, creative approaches to finding cures for persistent diseases. Our mission is to work with passion and purpose every day to improve lives. We are looking for individuals who value this pursuit and want to make a difference for patients and their caregivers. In Clinical Operations, you will contribute to advancing clinical research in diverse therapeutic areas, including Oncology. We offer a supportive and team-oriented environment with extensive support for regulatory submissions, TMF management, and in-house CRAs. We provide regular touchpoints and coaching with your Line Manager to ensure professional development, offering 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. You will have the opportunity to drive scientific breakthroughs and be at the core of successful clinical trials.

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, 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.
• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Associate degree