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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 at www.abbvie.com. Follow @abbvie on X (https://twitter.com/abbvieireland) , Facebook, Instagram (https://www.instagram.com/abbvieireland/) , YouTube and LinkedIn.

Job Description

Thank you for considering a future opportunity with our company! We are not currently hiring for this specific role, but we would love to connect with talented individuals who are interested in potential future positions. By joining our talent pipeline, you will be the first to be notified when suitable opportunities arise.

In this talent pipeline requisition, we are not actively recruiting for this position at the moment. However, we are building a network of exceptional individuals who possess the skills and experience required for future openings. By submitting your application to this requisition, you will be added to our talent pipeline and considered for future opportunities.

Medical Directors within the Patient Safety, Epidemiology and Quality team are responsible for the following:

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

2.  Responsible for safety surveillance for pharmaceutical / biological / drug –device combined early oncology product and implementing risk management strategies for assigned product

3.  Lead, set the strategy in collaboration with the development medical lead of study protocols and informed consents. When appropriate write the key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses, aggregate reports.

4.  Apply current regulatory guidance as appropriate for safety surveillance and authorship of safety documents. Analyze, interpret, and summarize aggregate safety data and communicate these analysis and interpretation to cross-functional teams and senior management

5.  Independently write, review, and provide input on technical documents. Oversight and responsibility for leading the strategy as well as writing, when applicable, the key sections for periodic reports (e.g. DSUR’s, PADER’s and Safety sections of the IBs)

6.  Opportunities to co-author publications and participate in initiatives to continue developing and growing as a safety leader

Qualifications

1.  MD / DO with 2+ years of residency with patient management experience

2.  5 - 8 years of Pharmacovigilance / Clinical Development experience in the pharmaceutical industry

3.  Effectively analyze and guide analysis of clinical data and epidemiological information

4.  Effectively present recommendations / opinions in group environment both internally and externally

5.  Write, review and provide input on technical documents

6.  Work collaboratively and lead cross-functional teams

Additional Information

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 https://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

Salary: $35,000 - $172,500