Job Summary
The Clinical Research Associate II is vital in overseeing and managing clinical trials, ensuring adherence to regulatory guidelines and protocols. This role demands a keen focus on maintaining data integrity and patient safety while facilitating communication between stakeholders throughout the study lifecycle.
Responsibilities
- Monitor clinical trial sites to ensure compliance with study protocols and regulatory requirements.
- Conduct regular site visits for the assessment of study progress and issue resolution.
- Manage and verify the accuracy of clinical data collected from sites.
- Facilitate effective communication between the project team, investigators, and regulatory bodies.
- Assist in the development and maintenance of study documentation and reports.
Qualifications
- Bachelor’s degree in life sciences or a related field.
- Proven experience as a Clinical Research Associate, preferably with a focus on Phase II and III trials.
- Strong knowledge of Good Clinical Practice (GCP) and other applicable regulations.
- Excellent communication skills, both written and verbal, with the ability to collaborate effectively.
- Proficiency in data management systems and Microsoft Office applications.
SUNY Upstate Medical University 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.
