Job Summary
The Clinical Research Associate (CRA) position focuses on enhancing global health outcomes through the management of clinical trials. This role involves close collaboration with biopharmaceutical companies and research sites, particularly within the oncology sector, to ensure successful study execution and adherence to regulatory standards.
Responsibilities
- Collaborate effectively with investigators and site staff to facilitate smooth trial operations.
- Review and monitor trial progress, ensuring compliance with regulatory requirements.
- Develop and maintain productive relationships with key stakeholders in clinical research.
- Assist in the design and implementation of clinical study protocols.
Qualifications
- Experience in clinical research, particularly in oncology, is preferred.
- Strong understanding of regulatory requirements and good clinical practices.
- Excellent communication and interpersonal skills to foster relationships with research personnel.
- Ability to work independently and remotely in a dynamic environment.
Parexel 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.
