Senior Clinical Research Associate - Oncology

Worldwide Clinical Trials • Durham, NC

6d • $1,000,000

About The Position

Worldwide Clinical Trials is hiring a Senior Clinical Research Associate to manage research activities at sites participating in its clinical research projects, with a focus on oncology. The role is part of Clinical Operations and involves working with colleagues across therapeutic areas in a collaborative, team-oriented environment. Site-management support includes regulatory submissions, Trial Master File (TMF) management, and in-house CRAs for projects with substantial site-management needs. The company also provides regular coaching and professional development, with a career path that may lead to Clinical Trial Manager roles.

The CRA is typically involved throughout the clinical study lifecycle: identifying potential sites, supporting study start-up by collecting regulatory documents and assisting with contract and budget negotiations, training site staff, managing site activities during study maintenance, and closing site activities after study completion. Most site-management work is performed remotely, but the CRA must help ensure informed-consent requirements, safety-event reporting, and applicable regulatory requirements are followed. The role includes conducting study initiation visits (SIVs), requires regional travel, and is open to candidates residing in the United States.

The stated annual salary range for the United States is $0 to $1,000,000. The posting says final compensation depends on relevant experience, performance, education, and internal equity, and that benefits vary by location. Worldwide Clinical Trials describes itself as an equal opportunity employer committed to an inclusive and equitable workplace.

Requirements

• At least 5 years of experience as a Clinical Research Associate.
• A four-year university degree or a nursing degree.
• Oncology experience.
• Excellent interpersonal, oral, and written communication skills in English.
• Strong organizational skills and attention to detail.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC systems.
• Residence in the United States.
• Willingness to travel regionally.

Responsibilities

• Manage research activities at sites participating in the company’s clinical research projects.
• Identify potential sites to participate in clinical research.
• Support study start-up, including collecting regulatory documents and assisting with contract and budget negotiations.
• Train sites to collect data properly and report potential safety-related events.
• Manage site activities during study maintenance.
• Close down site research activities after a study concludes.
• Conduct study initiation visits (SIVs).
• Help ensure informed-consent requirements, potential safety-event reporting, and applicable regulatory requirements are followed.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior