Job Summary
The Clinical Research Associate for Translational Research in Oncology (TRIO) is part of a global organization focused on promoting advancements in translational research within the oncology field. This role is essential for driving clinical initiatives and enhancing health outcomes through targeted research efforts.
Responsibilities
- Participate in the development and implementation of clinical research protocols.
- Monitor clinical studies and ensure compliance with regulatory standards and protocols.
- Coordinate data collection and management to support research objectives.
- Collaborate with cross-functional teams to facilitate study progress.
Qualifications
- Degree in a relevant field such as Medical, Nursing, Pharmacy, or Health Science, or equivalent international qualification.
- Experience in clinical research is preferred but not explicitly stated.
- Strong understanding of compliance regulations and clinical trial management.
Translational Research in Oncology 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.
