Job Summary
In the role of Senior Clinical Research Associate focusing on CNS and Psychiatry, you will be instrumental in enhancing the standards of clinical research within Worldwide Clinical Trials. This position allows for a significant impact on the research process while collaborating with diverse teams and engaging with investigative sites across the East Coast. The position is entirely remote, providing flexibility while maintaining a commitment to clinical excellence.
Responsibilities
- Conduct monitoring visits at investigative sites to ensure adherence to study protocols and regulations.
- Collaborate with cross-functional teams to facilitate efficient site operations.
- Provide training and guidance to site personnel and ensure that clinical data is accurate and complete.
- Support the development of project-related documents and contribute to study integrity and compliance.
- Travel to assigned sites approximately 8-10 times per month for in-person assessments and meetings.
Qualifications
- Possess a degree from a four-year university or hold a Nursing degree.
- Have a minimum of 5 years of experience in clinical research, preferably within psychiatry or CNS.
- Demonstrate strong knowledge of GCP, ICH guidelines, and relevant regulations.
- Exhibit excellent communication and organizational skills to manage multiple assignments effectively.
- Show capability in building robust relationships with sites and stakeholders involved in the research process.
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.
