Future Opportunities - Join Our Talent Pipeline for Medical Directors- Patient Safety
Future Opportunities - Join Our Talent Pipeline for Medical Directors- Patient Safety
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Salary Not Disclosed
1 Vacancy
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:
and application of the pharmacology chemistry and nonclinical toxicology to effectively conduct safety surveillance
for safety surveillance for pharmaceutical / biological / drug device combined early oncology product and implementing risk management strategies for assigned product
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.
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 crossfunctional teams and senior management
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. DSURs PADERs and Safety sections of the IBs)
to coauthor publications and participate in initiatives to continue developing and growing as a safety leader
Qualifications :
/ DO with 2 years of residency with patient management experience
2.5 8 years of Pharmacovigilance / Clinical Development experience in the pharmaceutical industry
analyze and guide analysis of clinical data and epidemiological information
present recommendations / opinions in group environment both internally and externally
review and provide input on technical documents
collaboratively and lead crossfunctional 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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Employment Type
Full-time
