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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 non-clinical 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 cross-functional 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 co-author 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 cross-functional teams
Additional Information :
Applicable 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 believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future. Salary: $35000 - $172500
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable 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 visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Full-time
Full-time