Scientific Director, Immunology, Global Patient Safety

• Supports the planning and execution of the safety strategy for immunology assets during the entire lifecycle of the drug
• Leads development and implementation of an asset safety strategy with support of PST-L or management
• Supports in the review and synthesis of scientific safety data for critical regulatory and clinical documents including IBs DSURs PSURs RMPs CSRs etc. - ensuring medical accuracy scientific rigor and clarity of content across immunology assets
• Facilitates scientific connections and interactions information exchange across assets within the safety teams
• Prepares material on competitive intelligence current disease state and standard of care for key indications/ disease states
• Compiles draft slide presentations for internal and external meetings as required
• Interacts with and influences other cross functional departments (e.g. Clinical Development Statistics Regulatory Affairs Clinical Pharmacology Medical Affairs) as needed to ensure the successful development design and implementation of comprehensive safety assessments to support study participants in immunology studies.
• Drives process improvement and change management for the Immunology Safety team in conjunction with enterprise-wide and functional area plans.
• Deep dive in literature search and capable to deliver a strong analysis and summary and proposal for any additional needed safety action

Qualifications :

• Scientific or clinical degree (e.g. NP/PA PharmD MS PhD MPH including combinations)
• At least 5 years of pharmaceutical industry experience preferably in patient safety/ PV
• Knowledge of clinical trial methodology regulatory and compliance requirements governing clinical trials and experience in development of clinical strategy and the design of study protocols
• Strategic thinking and capacity of analyzing aggregate data and conclude
• Effectively present recommendations / opinions in group environment both internally and externally
• Ability to work effectively under circumstances of uncertainty and complexity.
• Proven ability to critically evaluate and interpret complex safety data from clinical trials supporting informed risk-benefit decision-making
• Strong ability to influence individual stakeholders and cross-functional teams in a collaborative environment
• Must possess excellent oral and written English communication skills.
• Work collaboratively and lead cross-functional teams
• Good communication and influence skills
• Good organization and mastering Microsoft office tools

Additional Information :

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 believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future. 

• 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 long-term incentive programs. 

Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.

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  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No

Employment Type :

Full-time