This position will be part of the Clinical Affairs Team, which is responsible for executing, managing and conducting projects associated with the company clinical study plans. The Sr. CRA is responsible for site management deliverables on assigned protocols. With minimal supervision, the Sr. CRA manages the clinical monitoring activities of the study and assures site compliance with study protocols and applicable regulations and assists the Clinical Study Manager with study related activities, as required. The Sr. CRA may act as a lead CRA for the Sponsor.
#LI-AS2 / This is a field based role.
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. Applicable portions of the Company’s affirmative action program are available to any applicant or employee for inspection upon request.