Future Opportunities - Join Our Talent Pipeline for Medical Directors- Patient Safety
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, Facebook, Instagram, 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 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 with the skills and experience required for future openings. By submitting your application, you will be added to our talent pipeline and considered for future opportunities.
Responsibilities of Medical Directors in Patient Safety, Epidemiology, and Quality:
Understanding and application of pharmacology, chemistry, and non-clinical toxicology to conduct safety surveillance effectively.
Responsible for safety surveillance for pharmaceutical/biological/drug-device combined early oncology products and implementing risk management strategies for assigned products.
Lead and set strategy in collaboration with the development medical lead for study protocols and informed consents. When appropriate, write key pharmacovigilance documents, including safety assessments, regulatory responses, and aggregate reports.
Apply current regulatory guidance for safety surveillance and authorship of safety documents. Analyze, interpret, and summarize safety data, communicating findings to cross-functional teams and senior management.
Independently write, review, and provide input on technical documents. Oversee and lead strategy, including writing sections for periodic reports like DSURs, PADERs, and Safety sections of IBs.
Opportunities to co-author publications and participate in initiatives to develop as a safety leader.
Qualifications:
MD / DO with 2+ years of patient management experience.
5-8 years of Pharmacovigilance / Clinical Development experience in the pharmaceutical industry.
Ability to analyze and guide analysis of clinical data and epidemiological information.
Effective presentation of recommendations/opinions internally and externally.
Experience in writing, reviewing, and providing input on technical documents.
Ability to work collaboratively and lead cross-functional teams.
Additional Information
Applicable only to applicants in locations with pay disclosure laws:
The salary range is $35,000 - $172,500, based on job grade, location, and other factors. Compensation may vary and is at the company's discretion.
We offer a comprehensive benefits package, including paid time off, medical/dental/vision insurance, and 401(k).
This role is eligible for participation in short-term incentive programs.
Note: Compensation is considered earned only when paid. The company reserves the right to modify compensation and benefits at its discretion.
AbbVie is an equal opportunity employer committed to integrity, innovation, and community service. We welcome veterans and individuals with disabilities.
For more information or to apply, visit
https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
or
https://www.abbvie.com/join-us/reasonable-accommodations.html .
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