Job Summary
The Clinical Research Associate II in Oncology is responsible for the oversight and management of clinical trials within the oncology therapeutic area. This role involves the execution of trial protocols and the supervision of study sites to ensure compliance with regulatory and company standards. The candidate will play a pivotal role in ensuring the integrity and quality of clinical data while contributing to the advancement of cancer treatments.
Responsibilities
- Monitor clinical trial sites to ensure compliance with study protocols and regulatory requirements.
- Conduct regular visits to assess study progress and data accuracy.
- Collaborate with investigational sites to ensure they have adequate training and resources to conduct trials.
- Assist in the preparation and review of study documentation and reports.
- Track site performance and ensure timely data entry and resolution of issues.
- Participate in training new staff and providing ongoing support for study procedures.
Qualifications
- A bachelor’s degree in a life science or related field.
- A minimum of 2 years of experience as a clinical research associate in oncology.
- Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements.
- Excellent communication and interpersonal skills to work effectively in a team environment.
- Proficiency in clinical trial management software and data reporting tools.
