Pennsylvania
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Onsite
Job description
Job Summary
The Senior Clinical Research Associate – Oncology will be responsible for overseeing and monitoring clinical trials in the oncology field, ensuring adherence to regulatory standards and promoting the highest quality of research. This role takes place onsite in Pennsylvania and is part of a global team at Worldwide Clinical Trials, dedicated to improving patient lives through innovative research.
Responsibilities
- Monitor clinical trial progress and ensure compliance with study protocols.
- Conduct site visits to assess performance and provide support to site personnel.
- Participate in the preparation of documentation for regulatory submissions.
- Collaborate with cross-functional teams to facilitate effective communication and project progress.
- Provide training and guidance to site staff regarding study protocols and regulatory requirements.
Qualifications
- Bachelor’s degree in a relevant field or a degree in nursing.
- Proven experience in clinical research, specifically within oncology.
- Strong understanding of clinical trial processes and regulatory guidelines.
- Excellent communication skills and the ability to work effectively in a team-oriented environment.
- Detail-oriented with strong organizational and time management abilities.
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.
