Director, Safety Data Sciences (people manager) 

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About the role

Purpose: This position partners with cross functional stakeholders in support of the product safety profile and benefit risk throughout product lifecycle through signal detection, signal evaluation, and preparation of written and verbal summaries of signal management activities and risks to patient safety to present to senior management and regulatory authorities globally.     Responsibilities:   • Responsible for oversight of surveillance and regulatory activities and deliverables in your designated Therapeutic Area (TA).   • Leads a team of Safety Data Sciences in their role on the Product Safety Team (PST) within a given TA; contributes to the benefit risk evaluation and to safety risk management.    • Provide oversight and actively manages full time employee (safety data scientists) and contract support personnel.   • Key collaborator with Therapeutic Area Heads, safety and clinical physicians and Data and Statistical Sciences to develop strategies for routine and ad hoc safety data analyses.   • Independently authors, strategizes and reviews global aggregate safety reports in accordance with regulatory requirements and standard operating procedures   • Utilizes medical judgment to determine the impact of the safety issue on the product’s benefit-risk profile.   • Collaborative preparation and maintenance of safety sections of Clinical Summary of Safety, Clinical Study Reports, Company Core Data Sheets and Risk Management Plans.    • Assure deliverable alignment to current company standards and global regulations for products/compounds assigned to direct reports.     • Leads safety-related activities/initiatives internal to PPS and with external partners.   • Independently prepares summaries of key safety data for PST, ADT, senior management, Advisory and other similar meetings.    • Trains new safety scientists and mentors established colleagues.  • Degree in a Health Sciences (e.g., Pharmacy, Epidemiology, Nursing);   • Bachelors + 7 years clinical/pharma or safety work experience  • Masters or doctorate + 5 years clinical/pharma or safety work experience (e.g. MPH, PharmD, or Masters in a Health Science)   • Knowledge of the drug development process which includes conducting clinical trials, scientific strategy and operations management for the planning, execution and reporting of clinical development programs, regulatory requirements for submission, product launch and post marketing support.    • Demonstrates ability to connect regulatory obligations and safety science to support safety decision making.    • Understanding of tools, standards and approaches used to efficiently evaluate drug safety.  • Experience in working directly with and influencing senior management including functional heads  • Identifies strengths and weaknesses of team members to further develop their skills through training, mentoring and learning opportunities.   • Optimizes use of team resources and ensures quality and timeliness in team contributions.   • Prior experience with people management desired.  • Identifies new partnerships throughout Abbvie to increase efficiencies  • Initiates strategic plans for deliverables and leads process improvements  • Effective oral and written communication skills with the ability to manage multiple projects simultaneously   • Microsoft WORD and EXCEL skills and Basic Project Management skills    • Able to work independently seeking guidance from manager and PST leads and TA physicians as needed.  Able to problem solve and anticipate problems.    Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​ • The compensation range described below is the range of possible base pay compensation that the Company beli

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