Job Summary
The Clinical Research Associate (CRA) is responsible for overseeing clinical trials and ensuring that the research processes comply with regulatory standards, protocols, and ethical guidelines. The CRA plays a key role in maintaining data integrity and participant safety within the trial environment. They work collaboratively with sponsors, clinical trial sites, and research organizations to facilitate the successful completion of clinical studies.
Responsibilities
- Monitor and manage clinical trial activities to ensure adherence to study protocols and regulatory requirements.
- Conduct site visits to assess study progress, evaluate site performance, and provide support to the study team.
- Verify data accuracy and completeness, and ensure timely reporting of study results.
- Collaborate with investigators and site staff to address any study-related issues and facilitate communication.
- Perform essential document reviews and maintain regulatory compliance throughout the study lifecycle.
- Assist in training site personnel regarding the study protocol and processes.
Qualifications
- Bachelor’s degree in a life science or related field.
- Previous experience in clinical research or a related medical field preferred.
- Strong knowledge of clinical trial regulations and guidelines (e.g., GCP, ICH).
- Excellent communication and interpersonal skills for effective collaboration with various stakeholders.
- Ability to work independently and manage multiple priorities within a fast-paced environment.
- Proficiency in clinical data management and analysis tools is advantageous.
ICON San Antonio 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.
