Job Summary
We are seeking a dedicated Senior Clinical Research Associate specialized in oncology to join our team in Durham, North Carolina. In this role, you will oversee and manage research activities across various clinical trial sites, ensuring that all processes are conducted effectively and in compliance with protocols.
Responsibilities
- Manage clinical trial activities at multiple sites, ensuring adherence to research protocols.
- Collaborate with site personnel and stakeholders to facilitate smooth trial operations.
- Monitor patient safety and data integrity throughout the trial process.
- Conduct site visits and inspections to assess compliance and engagement.
- Assist in the preparation and review of trial documentation and reports.
Qualifications
- Approximately 4 years of experience as a Clinical Research Associate.
- Possess a bachelor’s degree in a relevant field or a nursing degree.
- Demonstrated experience in conducting oncology clinical trials.
- Strong knowledge of clinical research regulations and guidelines.
- Excellent communication and organizational skills.
Worldwide Clinical Trials provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
