Job Summary
The Senior Clinical Research Associate in the CNS domain plays a pivotal role in ensuring the smooth execution of clinical trials. Operating from Minnesota, this position requires a focus on high-quality research while collaborating closely with investigative sites and study teams. The selected candidate will be dedicated to maintaining excellence in clinical study management and will act as a primary liaison for all site-related activities.
Responsibilities
- Facilitate the monitoring of clinical trial sites to ensure adherence to study protocols and regulatory requirements.
- Collaborate with investigational sites to support study enrollment and data collection efforts.
- Assist in training and onboarding of site staff regarding study procedures and protocols.
- Ensure completeness and accuracy of clinical trial documentation.
- Conduct regular site visits and provide timely feedback to the study teams.
Qualifications
- A Bachelor’s degree or a Nursing degree is essential.
- Relevant experience in clinical research, specifically in CNS studies is preferred.
- Strong interpersonal and communication skills to effectively interact with various stakeholders.
- Ability to work independently while managing multiple tasks efficiently.
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.
