The Sr. Clinical Research Associate (Sr. CRA) assists in the planning, development and execution of clinical research studies under only general supervision, in accordance with applicable global regulatory requirements and company policy. This role may serve as the lead for a designated study or manage a group of research sites, developing and maintaining successful working relationships with internal and external partners, defining and implementing project scope, deliverables, risk mitigation strategies and issue resolution. The Sr. CRA ensures compliance to the study protocol and proactively drives progress to activation, enrollment and data quality milestones by leveraging study and site-level metrics. The candidate must possess strategic thinking, effective communication and data-driven leadership.
Essential Duties and Responsibilities:
Knowledge, Skills, and Abilities Required for Successful Job Performance:
You take care of Zoll | Respicardia and we'll take care of you!
ZOLL appreciates and values diversity. We are an equal opportunity employer and do not discriminate in hiring or employment on the basis of race, color, religion, national origin, citizenship, gender, gender
identity, genetic information, marital status, sexual orientation, age, disability, veteran status, or any other characteristic protected by federal, state, or local law.
ADA: ZOLL will make reasonable accommodations in compliance with the Americans with Disabilities Act