Job Summary
The Clinical Research Associate (CRA) plays a crucial role in overseeing clinical trials and ensuring compliance with regulatory standards. This position involves monitoring the progress of clinical studies, coordinating with investigators and site staff, and maintaining quality in data collection and reporting procedures.
Responsibilities
- Oversee site selection, initiation, and monitoring throughout the course of clinical trials.
- Ensure adherence to study protocols and regulatory requirements.
- Conduct regular visits to clinical sites to assess adherence to protocols and manage source documentation.
- Facilitate communication between the study sponsors, investigators, and site personnel.
- Perform data verification and contribute to the resolution of discrepancies.
- Assist in the preparation of study-related documents and reports as required.
Qualifications
- A bachelor’s degree in life sciences or a related field is typically required.
- Experience in clinical research or as a CRA is highly preferred.
- Strong understanding of Good Clinical Practice (GCP) and regulatory guidelines.
- Excellent organizational and communication skills.
- Ability to work independently and manage multiple projects simultaneously.
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.
