Job Summary
The Clinical Research Associate (CRA) plays a pivotal role in overseeing and managing clinical trials. This position is responsible for ensuring that studies adhere to regulatory standards and are conducted according to the outlined protocols. A CRA will also collaborate closely with clinical teams, principal investigators, and other stakeholders to facilitate the successful execution of clinical studies.
Responsibilities
- Monitor clinical trials to ensure compliance with regulatory guidelines and protocols.
- Conduct site visits to assess study progress and provide guidance to site staff.
- Collect, validate, and manage clinical data to ensure accuracy and completeness.
- Prepare and maintain essential study documentation, including monitoring reports.
- Collaborate with investigators and site personnel to troubleshoot issues and enhance study operations.
- Assist in the training of site staff on study protocols and procedures.
Qualifications
- A degree in life sciences or a related field.
- Previous experience as a Clinical Research Associate or in a similar role is preferred.
- Strong understanding of GCP, ICH guidelines, and regulatory requirements.
- Excellent organizational skills and attention to detail.
- Strong communication skills, both written and verbal.
- Proficiency in data management and clinical trial software.
ICON plc 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.
