Remote Senior CRA - CNS & Oncology (Midwest)

Worldwide Clinical Trials; Asheville (NC); Remote; USD 85,000 - 125,000; Full time

Job summary

Worldwide Clinical Trials in the Midwest United States is seeking a Senior Clinical Research Associate focused on CNS and oncology studies. You will manage site activities across clinical trials, conduct study initiation visits, and ensure regulatory compliance while working remotely.

You will monitor site performance, support contract negotiations and budgets, train sites on data collection and safety reporting, and ensure informed consent and regulatory requirements are met throughout studies.

Qualifications

• 5+ years of Clinical Research Associate experience.
• Bachelor's degree or nursing degree required.
• CNS and oncology therapeutic area experience required.
• Proficiency in Microsoft Office, CTMS, and EDC systems.
• Excellent written and verbal communication skills in English.
• Strong organizational skills with meticulous attention to detail.
• Current residence in Midwest United States with regional travel capability.

Responsibilities

• Manage research activities and compliance at participating clinical trial sites
• Conduct study initiation visits and oversee site setup activities
• Support contract negotiation, budget management, and regulatory document collection
• Train sites on proper data collection and safety event reporting procedures
• Monitor site compliance with informed consent and regulatory requirements throughout studies

Skills

CRA experience

English communication

Organizational skills

Travel readiness

Education

Bachelor's degree

Nursing degree

Tools

Microsoft Office

CTMS

EDC systems

Job description

Worldwide Clinical Trials in the Midwest United States is seeking a Senior Clinical Research Associate focused on CNS and oncology studies. You will manage site activities across clinical trials, conduct study initiation visits, and ensure regulatory compliance while working remotely.

You will monitor site performance, support contract negotiations and budgets, train sites on data collection and safety reporting, and ensure informed consent and regulatory requirements are met throughout studies.