AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.
This position supports the case processing organization to achieve its mission of improving patient lives globally through industry leading safety and compliance by consistent and accurate delivery of high quality, relevant and timely adverse event information. Collect, assess and process adverse event information (clinical and post marketing) in a compliant and timely manner in order to comply with global regulations which includes: Seriousness assessment Labeling, Casuality, Initial and Follow- up Meeting company standards for quality, compliance and productivity. Remaining current on knowledge and skills required for case processing. Understanding of the changing regulatory environment and the impact to the case management process Meets case quality, case processing metrics and agility by exhibiting the Abbvie core leadership attributes: Agile and Accountable; Clear and Courageous; Make Possibilities Real; All for One AbbVie; Decide Smart and Sure Supporting and participating in audits and inspections as needed Begins mentoring MSA’s in case processing in their primary area PMS or Clinical Participation in project work as work volume allows Developing cross functional relationships and effectively communicate with internal and external partners Assumes responsibility to manage case processing case load, additional duties and project work assigned Other duties may be assigned based on the need or work requirement of the organization
Basic: Minimum: Bachelor’s degree with related health sciences background, RN, BSN, BS, BS Pharm. PharmD or advanced degree preferred. Candidates lacking the appropriate degree but with previous pharmaceutical experience may be considered 3-5 years drug safety experience minimum Demonstrated ability to lead project work. Proven success in results-driven process management Core knowledge of industry regulations (ICH, FDA, EMEA, MHRA) Proficient in case processing processes, procedures, conventions
Significant Work Activities
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Keyboard use (greater or equal to 50% of the workday)
Job Level Code
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis 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, protected veteran status, or any other legally protected characteristic.