Provide leadership and direction to clinical site management team members from study start through to closure
Serve as Site Management’s primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to Primary Sponsor Contact
Manage monitoring deliverables to achieve the study budget and identify out-of-scope activities
Requirements
Bachelor’s Degree or a Nursing Degree required
1+ years’ experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role
3+ years’ experience as a Clinical Research Associate
CNS/Neurology experience is required
Experience in Multiple Sclerosis and/or Alzheimer's Disease a plus
Willingness to travel up to 30%
Benefits
We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.
We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.