Sr Medical Director - Baltimore, United States - Allergan

Description

Company DescriptionAbbVie'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 .Job DescriptionServe as Indication Product Safety Lead for one or more products or product indications under the direction of the Therapeutic Area (TA) Lead and Global TA.

Ensuring safety of one or more products through the product lifecycle (e.g. surveillance, signal detection, validation and assessment). Interpreting regulations related to pharmacovigilance supporting all patient safety activities.


Responsibilities:

Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillanceResponsible for safety surveillance for pharmaceutical / biological / drug device combined productsLead, set the strategy and when appropriate write the key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses, 15 day aggregate reports.

Apply current regulatory guidance as appropriate for safety surveillance and authorship of safety documentsAnalyze, interpret, and summarize aggregate safety data and communicate these analysis and interpretation to cross-functional teams and senior managementIndependently write, review, and provide input on technical documentsOversight and responsibility for leading the strategy as well as writing, when applicable, the key sections for periodic reports (e.g. PSURs,DSURs, PADERs and Safety sections of the IBs)

Lead and set the strategy, in collaboration with the development medical lead of study protocols and informed consentsResponsible for implementing risk management strategies for assigned productProactively engaging, inspiring, coaching and mentoring team members and colleaguesOpportunities to co-author publications and participate in initiatives to continue developing and growing as a safety leaderSignificant Work ActivitiesContinuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is requiredFrequent to continuous computer usage (greater or equal to 50% of the workday) is requiredQualificationsMD / DO with 2+ years of residency with patient management experience; Master Public Health is preferred in addition to MD / DO, not required- 8 years of Pharmacovigilance / Clinical Development experience in the pharmaceutical industryEffectively analyze and guide analysis of clinical data and epidemiological informationEffectively present recommendations / opinions in group environment both internally and externallyWrite, review and provide input on technical documentsWork collaboratively and lead cross-functional teamsAbility to lead cross-functional team in a collaborative environmentEvaluate and make independent decisionsEffectively present recommendations / opinions in group environment both internally and externallyAdditional InformationApplicable 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 believesingood faith it will pay for this role at the time of this posting based on the job grade for this position.

Individualcompensation paid within this range will depend on many factors including geographic location, and we mayultimatelypay 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/visioninsurance 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 payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.

The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensationand benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid andmay be modified at the Companys sole and absolute discretion, consistent with applicable law.

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

It is AbbVies 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.

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