Job Summary
The Oncology Clinical Research Associate (CRA) plays a vital role in the development and management of clinical trials focused on oncology. This position involves overseeing trial protocols, ensuring compliance with regulatory requirements, and facilitating smooth execution of studies dedicated to cancer research.
Responsibilities
- Monitor and evaluate ongoing clinical trials, ensuring adherence to protocols and regulatory guidelines.
- Conduct site visits and maintain productive relationships with investigators and site staff.
- Collect and review clinical data for accuracy and completeness.
- Assist in the training and support of site personnel on study protocols and procedures.
- Prepare and submit reports on study progress and participant recruitment to ensure project timelines are met.
Qualifications
- Bachelor’s degree in Life Sciences, Nursing, or a related field.
- Experience in clinical research, preferably within oncology.
- Strong understanding of GCP, ICH guidelines, and regulatory requirements.
- Excellent communication skills and ability to work collaboratively in a team environment.
- Proficiency in data management and analysis tools relevant to clinical research.
