Director, Safety Statistics Group Oncology TA Head
Director, Safety Statistics Group Oncology TA Head
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1 Vacancy
Job Description
The Safety Statistics Group (SSG) at AbbVie is an important strategic part of Data and Statistical Sciences (DSS). Safety Statisticians are part of collaborative cross functional teams including members from Pharmacovigilance and Patient Safety (e.g product safety team physicians epidemiologists safety analysts) Statistical Programming Clinical Statistics Regulatory Affairs and Medical Writing. Safety Statisticians work on products in the AbbVie portfolio ranging from early to later stages of development and life cycle management with a focus on evaluation interpretation and reporting of aggregate/integrated safety data including benefit risk planning and assessment.
AbbVie is seeking an experienced statistician to serve a Safety Statistics Group Oncology TA Head in our Safety Statistics team. The Director will have oversight of statisticians in oncology.
Key Responsibilities:
- Provide strategic input to and oversight of the development of Product Safety Statistical Analysis Plans (PSSAPs) and Integrated Summary of Safety Statistical Analysis Plans (ISS SAPs).
- Ensure consistency across documents (eg PSSAP study SAPs ISS SAP).
- Provide strategic input on safety related submissions to regulatory agencies and responses to requests from regulatory agencies.
- Attend regulatory meetings.
- Oversight of the development of safety data integration specifications in accordance with analysis plan.
- Lead and provide oversight of contributions by Safety Statistics to benefit-risk planning and assessment including ensuring delivery and interpretation of benefit-risk data displays/analyses.
- Oversight of the development delivery and interpretation of safety outputs including graphics.
- Oversight of cross-functional development of output specifications to address both pre-planned safety analyses and ad hoc requests.
- Oversight to ensure the delivery of high-quality outputs according to agreed-upon timelines.
- Ensure appropriate interpretation of safety deliverables in collaboration with other functions.
- Identify potential areas to improve processes or statistical methodologies initiate steps to evaluate possible improvements and develop a plan to implement changes based on this evaluation.
- Lead within-SSG initiatives and represent SSG on cross-functional efforts to implement strategic initiatives that address processes related to monitoring assessing interpreting and reporting safety data.
- Stay current with industry trends and practices related to safety.
- Potentially represent SSG/DSS on external initiatives to advance the drug safety analytics discipline (eg ASA PhUSE DIA etc.) depending on individual interests.
- Responsible for project and resource management within SSG for therapeutic area(s) of responsibility.
- Mentor team members and provide appropriate development opportunities.
Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required
Qualifications :
- MS (with at least 14 years of experience) or PhD (with at least 10 years of experience) in Statistics Biostatistics.
- Minimum of 2 years of management experience required for people managers.
- Excellent communication skills both oral and written
- Advanced knowledge of statistical methodology including experimental design descriptive statistics inferential statistics and statistical programming.
- Must have demonstrated exemplary statistical experience in managing and completing multiple projects or equivalent experience.
- In-depth knowledge and understanding in application of standard business procedures (regulatory guidance global regulations ethical issues assoc/iated with scientific research trials SOPs etc.).
- Experience interacting with regulatory agencies.
- Experience in leading NDA BLA and or CTD submission preferred.
- Oversight of multiple safety-related projects (eg ISS benefit-risk assessment signal detection).
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 short-term incentive programs.
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.
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No
Employment Type :
Full-time
Employment Type
Full-time
