Job Summary
The Clinical Research Associate II in Oncology plays a vital role in the management and oversight of clinical trials within the oncology department. This position is essential for ensuring research compliance, enhancing data integrity, and supporting the advancement of oncology studies through rigorous monitoring and coordination of trial activities.
Responsibilities
- Oversee and manage all aspects of clinical trials, ensuring compliance with regulations and protocols.
- Conduct site visits to monitor data collection and verify compliance with Good Clinical Practice (GCP).
- Engage with clinical sites to ensure proper patient recruitment and retention.
- Support the preparation of study-related documentation, including protocols and informed consent forms.
- Assist in the training and mentoring of junior research staff.
- Collaborate with cross-functional teams to facilitate successful trial execution.
Qualifications
- Bachelor’s degree in life sciences or a related field.
- Minimum of two years of experience in clinical research, preferably in oncology trials.
- Thorough understanding of clinical research regulations and GCP.
- Strong organizational skills and the ability to manage multiple projects simultaneously.
- Excellent communication and interpersonal skills.
- Proficient in data management systems and clinical trial management software.
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.
