Project Manager CTIS, Trial Disclosure (Drugs & Devices)

Key Responsibilities:
- Manage and provide oversight for global public disclosure of clinical trial data/information in compliance with requirements/commitments (e.g., CTIS, EUDAMED, EU Clinical Trial Regulation, EU Medical Device Regulation, EU In-vitro Device Regulation, EMA Policies 0043 & 0070, PhRMA/EFPIA Principles for Responsible Clinical Trial Data Sharing).
- Investigate and gather global requirements; implement processes to ensure accuracy, consistency, and alignment of clinical data/information made public.
- Work globally and cross-functionally to align procedures and ensure appropriate compliance.

Qualifications:
- Bachelor’s degree.
- 4 years submitting clinical trial registrations on behalf of sponsors and managing communications with regulatory authorities to make public an authorized clinical trial record.
- 2 years preparing and presenting oral and written presentations to peers, leadership, and business stakeholders; working in collaborative, cross-functional teams.
- 1 year serving as a project manager in the pharmaceutical industry (experience may be concurrent).

Benefits (if part of the job description): Paid time off (vacation, holidays, sick), medical/dental/vision insurance, 401(k); eligible for short-term and long-term incentive programs.

Application Instructions:
- Apply online at https://careers.abbvie.com/en or send resume to Job.opportunity.abbvie@abbvie.com. Refer to Req ID: REF49814Y.