Project Specialist/ Senior Project Specialist - North Chicago, IL, United States - Abbvie

Description

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.

We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.

For more information about AbbVie, please visit us at Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.
The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. The Regulatory Affairs Associate is responsible for providing operational support as required to the CTS managers / senior managers.

Operational support to CTS Leads for submission preparation and processing of initial CTA applications, amendments, end of trial notifications etc.

Review of and input into documents related to clinical trial submissions managed by other stakeholders such as IB and Protocols.

as well as operational support for Regulatory submission preparation and processing of amendments.

Populate relevant databases, activity trackers and questions database within agreed timelines and compliance/reporting requirements, and provide operational support for Regulatory and/or non-Regulatory systems that are critical for CTA submission and maintenance activities.

Provide technical support on document preparation e.g. Excel spreadsheets, Power point presentations.
Undertake all necessary training in order to achieve compliance with internal/external processes.
Provide operational support for the Clinical Trial Strategy & Submissions team.

Comply with the company's policies and procedures to meet statutory, quality and business requirements within the overall strategy and objectives of AbbVie Ltd.

Bachelor's degree in medicine, pharmacy, biology, chemistry, pharmacology, or related life sciences subject is required.
1-2 years Regulatory Affairs or R&D experience preferable.
~ Good Information Technology skills, proven ability to utilise a variety of computer application packages, such as MS Word, Excel, PowerPoint, Adobe Acrobat and global databases.
~ fluency in English.
~ Strong Project Management skills, able to manage multiple activities in line with business priorities and study time goals

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 incentive programs. ​

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.

It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.