Job Summary
The Senior Clinical Research Associate (CRA) – CNS position at Worldwide Clinical Trials involves a dedicated focus on delivering high-quality clinical research services. This role emphasizes the importance of collaboration as a trusted partner to investigative sites and study teams, ensuring that all processes meet industry standards and regulatory requirements. The selected candidate will play a vital role in supporting clinical trial operations, particularly in the central nervous system therapeutic area.
Responsibilities
- Ensure effective communication and collaboration with investigative sites.
- Monitor study progress and compliance with protocols and regulations.
- Assist in training site personnel on study protocols and procedures.
- Manage site visits, including pre-study, initiation, and monitoring visits.
- Review and validate the accuracy and quality of study data.
- Prepare and maintain study documentation and reports.
Qualifications
- A Bachelor’s degree in a relevant field or a Nursing degree is required.
- Previous experience in clinical research, with a preference for CNS studies.
- Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
- Excellent organizational and communication skills.
- Ability to work independently and as part of a team.
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.
