Job Summary
The Senior Clinical Research Associate focuses on Alzheimer’s Disease and is based in Western Springs, Illinois. This role is essential in providing expertise in clinical research, regulatory sciences, quality assurance, and compliance while overseeing monitoring and co-monitoring activities associated with clinical trials.
Responsibilities
- Oversee and conduct monitoring and co-monitoring visits for assigned clinical studies.
- Manage the lifecycle of investigational supplies, including preparation, dispatch, monitoring, and return.
- Ensure compliance with all relevant regulations and guidelines throughout the research process.
- Contribute to the development of clinical research strategies pertaining to Alzheimer’s Disease.
Qualifications
- Proven experience in clinical research, particularly in Alzheimer’s Disease or related fields.
- Strong knowledge of regulatory requirements and standards in clinical trials.
- Demonstrated ability to manage investigational supplies and monitor compliance activities.
- Effective communication skills to collaborate within multidisciplinary teams.
ProPharma Group 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.
