North Carolina
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Onsite
Job description
Job Summary
As a Senior Clinical Research Associate specializing in Oncology at Worldwide Clinical Trials, located in North Carolina, you will join a dedicated team committed to enhancing patient outcomes and driving innovation in clinical research. This role involves overseeing trials and ensuring adherence to quality standards while working onsite.
Responsibilities
- Manage and oversee clinical trials to ensure compliance with protocols, regulations, and quality standards.
- Collaborate with cross-functional teams to facilitate project success and improve patient outcomes.
- Provide guidance and support to junior staff and investigators during the trial process.
- Monitor trial progress, maintaining accurate documentation and timely reporting of issues.
- Engage with stakeholders to foster productive relationships and enhance trial efficiency.
Qualifications
- A bachelor’s degree from an accredited university or a degree in nursing.
- Demonstrated experience in oncology clinical research is essential.
- Strong organizational skills and attention to detail.
- Excellent communication abilities, both verbal and written.
- Proficiency in clinical research methodologies and regulatory requirements.
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.
