Investigate & gather global requirements & implement processes for ensuring accuracy, consistency, & alignment of clinical data/information made public.
Work globally & cross functionally to align procedures & ensure appropriate compliance.
Education & Experience
Must possess a Bachelor's degree.
Of the work experience required, must have 4 years submitting clinical trial registrations on behalf of clinical trial sponsors & managing communications with the regulatory authorities to successfully make public a record (i.e. registration) of an authorized clinical trial.
Of the experience required, must have 2 years:
preparing & presenting, orally & in writing, presentations to peers, leadership & business stakeholders; &
working in collaborative, cross-functional teams.
Of experience required, must have 1 year serving as a project manager in the pharmaceutical industry.
Work experience may be gained concurrently.
Salary Range: $153,712.00 - $157,500.00 per year.
Apply online at https://careers.abbvie.com/en or send resume to Job.opportunity.abbvie@abbvie.com . Refer to Req ID: REF49814Y
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term and long-term incentive programs.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
Abbvie · North Chicago, IL