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Pharmacoepidemiologist

Swiftwater, PA, United StatesRemoteFull-time

AI Summary

Designs and conducts post-authorization safety studies for vaccines, evaluates safety signals, and supports risk management and benefit-risk assessments within a global pharmacovigilance team.

About this role

Pharmacoepidemiologist

Pharmaceutical / Biotech

Pharmacoepidemiologist

Swiftwater Pennsylvania





Exp 2-5 yrs

Deg Bach

Relo

Bonus

Travel Occasional


Job Description


The Pharmacoepidemiologist is part of a dynamic Global Pharmacoepidemiology and Risk Management team within Global PharmacoVigilance Department (GPV) at Sanofi Pasteur. The main activities managed by the Pharmacoepidemiologist are:


• To design scientifically valid observational Post-Authorization Safety Studies (PASS) to fulfill Sanofi Pasteur’s post-marketing commitments using Good Pharmacoepidemiology Practices (GPP) and European Network of Centres for Pharmacoepidemiology and Pharmacovigilance (ENCEPP) methodological guidelines


• Works closely with the Product Safety Officers (PSO) in the respective Safety Evaluation Group to support safety signal evaluation in internal and external databases (WHO Vigibase, US VAERS)


• Provides input into benefit-risk assessment for vaccines (both qualitative and quantitative) as required by the EMA’s New Pharmacovigilance Legislation


• To bring epidemiological perspective, expertise and evidence-based recommendations in the identification and design of risk management plans (RMP), periodic risk-benefit evaluation reports (PBRER), and Safety Analysis Reports (SAR). He/she designs additional pharmacovigilance activities and risk minimization measures in RMP.


• Assists in the evaluation of external data sources for their utility in addressing vaccine safety related issues


• Provides background incidence rates of diseases, symptoms, and syndromes that are potential or identified safety risks. These rates may not be available and may require analysis of large observational / administrative databases.


• Provides critical review of relevant published literature


• Builds and maintains effective partnership with Global Medical Affairs, US Medical Affairs, Clinical Development and Regulatory Affairs departments


• Assists in the development of SOPs and Working Instructions


• Participates in ad-hoc requests or other activities as needed. These may include, but are not limited to teleconferences with the Health Authorities to discuss a pertinent safety issue, helping to maintain administrative database updates, and serving on internal or external workgroups.


Qualifications

A Doctorate of Philosophy (Ph.D) degree is required, Epidemiology concentration preferred along with a minimum of two (2) years pharmacoepidemiology or pharmacovigilance experience in industry.


ADDITIONAL SKILLS/PREFERENCES


• Effective communication of epidemiological strategy and findings, both written and verbal, is required.


• Self-motivated with the ability to work independently, to develop credibility with colleagues within and outside Epidemiology, and to influence decisions


• Knowledge of infectious diseases and vaccines is a plus


• Good knowledge of biostatistical principles and applications


• A sophisticated understanding of and the ability to interpret quantitative methods is required


• Working knowledge of statistical analysis softwares (SAS, STATA)


• Experience in strategic planning and project management


• Strong communications and organizational skills


• Experience and proficiency working in cross-cultural/global teams.

Primary Location: United States-Pennsylvania-Swiftwater


Other Locations: France-Rhone-Alpes-Lyon, Canada-Ontario-Toronto


Additional Information

All your information will be kept confidential according to EEO guidelines.

Direct Staffing Inc


Skills

ENCEPP GuidelinesGood Pharmacoepidemiology Practices (GPP)PharmacoepidemiologyPharmacovigilancePost-Authorization Safety Studies (PASS)Project ManagementSASSTATAVAERSWHO Vigibase

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