Job Summary
The Senior Clinical Research Associate (CRA) position focuses on psychiatric studies in the Southeast region. This role is pivotal in overseeing clinical trials aimed at evaluating new treatments. The Senior CRA will ensure compliance with regulatory standards while supporting investigative sites and maintaining the quality of data collection.
Responsibilities
- Manage the preparation and execution of clinical study monitoring visits.
- Coordinate with investigative sites to guarantee adherence to study protocols.
- Review collected data for accuracy and completeness.
- Support the training and guidance of junior staff and site personnel.
- Maintain up-to-date knowledge of clinical trial regulations and guidelines.
- Facilitate communication between sponsors, investigators, and regulatory agencies.
- Assist in the development of study documentation and reports.
Qualifications
- Bachelor’s degree in life sciences or relevant field; advanced degree preferred.
- Proven experience as a Clinical Research Associate, particularly in psychiatric studies.
- Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
- Excellent organizational and communication skills.
- Ability to work independently and collaboratively within a team.
- Proficiency in using clinical trial management software and tools.
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.
