Job Summary
The Senior Clinical Research Associate (CRA) specializing in Oncology plays a pivotal role in overseeing clinical trials in the Midwest region of the United States. This position is focused on ensuring the compliance and quality of data collected during the research process, contributing to the advancement of cancer treatment and therapies.
Responsibilities
- Manage and monitor clinical trials to ensure adherence to protocols and regulatory guidelines.
- Evaluate data from clinical sites to maintain accuracy and integrity throughout the study duration.
- Collaborate closely with investigators and site staff to resolve issues and enhance trial operations.
- Conduct site visits to train and support clinical personnel involved in the study.
- Contribute to the development and review of study documents, including protocols and informed consent forms.
Qualifications
- A Bachelor’s degree in life sciences or a related field; advanced degrees are preferred.
- Significant experience in clinical research, with a strong emphasis on oncology studies.
- Deep understanding of regulatory requirements pertinent to clinical trials.
- Exceptional organizational skills and attention to detail to manage multiple projects simultaneously.
- Strong interpersonal and communication skills for effective collaboration with teams and stakeholders.
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.
