Director/Sr Medical Director, Medical Safety Evaluation, Immunology-Remote

Allergan; Greenlawn (NY); Remote; USD 100,000 - 160,000; Full time

Job summary

An established industry player is seeking a dedicated Indication Product Safety Lead to oversee safety surveillance for innovative pharmaceutical products. This role involves collaborating with cross-functional teams, analyzing safety data, and authoring key regulatory documents. The ideal candidate will possess a strong background in pharmacovigilance and clinical development, along with excellent communication skills to effectively present findings. Join a forward-thinking company committed to transforming lives through innovative medicines and solutions.

Benefits

Paid Time Off

Medical/Dental/Vision Insurance

401(k) Plan

Short-term Incentive Programs

Long-term Incentive Programs

Qualifications

• 2+ years of residency with patient management experience.
• 5-8 years of experience in Pharmacovigilance or Clinical Development.

Responsibilities

• Lead safety surveillance for pharmaceutical products.
• Analyze and summarize safety data in compliance with regulations.

Skills

Pharmacovigilance

Clinical Development

Data Analysis

Communication Skills

Team Leadership

Education

MD / DO

Master in Public Health

Job description

Company Description

AbbVie'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 atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik Tok.

Job Description

Serve as Indication Product Safety Lead for one or more products under the direction of Group Medical Director Medical Safety Evaluation. Supporting assigned product with safety expertise through its lifecycle (including during the time of clinical development, marketing registration and post marketing), Interpreting, summarizing and presenting safety data in compliance with the regulatory guidelines.

Responsibilities:

•Understanding and application of pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance

•Responsible for safety surveillance for pharmaceutical / biological / drug –device combined products

•Leading, setting the strategy and, when appropriate, authoring the key documents with safety data, including but not limited to, medical safety assessments, parts of submission dossier and regulatory responses.

•Applying current regulatory guidance as appropriate for safety surveillance

•Analyzing, interpreting, and summarizing aggregate safety data and communicating these analysis and interpretation to cross-functional teams and senior management

•Independently writing, reviewing, and providing input on technical documents

•Providing oversight, leading the strategy as well as authoring when applicable, the key sections for periodic reports (e.g. PSURs, DSURs, PADERs and Safety sections of the IBs)

•Leading and setting the strategy, in collaboration with the development medical lead of study protocols and informed consents

•Defining and implementing risk management strategies for assigned product/indication

•Proactively engaging, inspiring, coaching and mentoring team members and colleagues

•Co-authoring publications and developing and growing as a safety leader

Significant Work Activities

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required

Frequent to continuous computer usage (greater or equal to 50% of the workday) is required

Qualifications

•MD / DO with 2+ years of residency with patient management experience; Master Public Health is preferred in addition to MD / DO, not required

•5 - 8 years of Pharmacovigilance / Clinical Development experience in the pharmaceutical industry or other relevant experience

•Effectively analyze and guide analysis of clinical data and epidemiological information

•Strong communicator, who is able to effectively present recommendations / opinions in group environment both internally and externally

•Write, review and provide input on technical documents

• Able work collaboratively and lead cross-functional team

•Formulates independent decisions

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemay ultimatelypay more or less than the posted range. This range may be modified in thefuture.

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.

• This job is eligible to participate in our short-term incentiveprograms.

• This job is eligible to participate in our long-term incentiveprograms

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 ofcompensation and benefitsthat are allocable to a particular employee remains in the Company's sole andabsolutediscretion unless and until paid andmay be modified at the Company’s sole and absolute discretion, consistent withapplicable 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, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

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

https://www.abbvie.com/join-us/reasonable-accommodations.html