Florida
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Onsite
Job description
Job Summary
The Senior Clinical Research Associate – Oncology role involves working with a dedicated team at Worldwide Clinical Trials, focusing on enhancing the quality of healthcare through innovative research. This position is based in Florida and requires an onsite presence, emphasizing the importance of direct collaboration in clinical environments. In this role, you will play a vital part in clinical trials, impacting patient lives by contributing to significant advancements in oncology research.
Responsibilities
- Oversee clinical trial operations and ensure compliance with regulatory requirements.
- Coordinate with various stakeholders to facilitate the smooth execution of clinical studies.
- Monitor study progress, manage data collection, and ensure accuracy in documentation.
- Support site staff and provide training on study protocols.
- Contribute to the preparation and submission of regulatory documents.
Qualifications
- A bachelor’s degree from a four-year university or a nursing degree is required.
- Proven experience in oncology clinical research is essential.
- Excellent communication and interpersonal skills to interact effectively with healthcare professionals.
- Strong organizational abilities and attention to detail.
- Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
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.
