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Job Requirements of Pharmacoepidemiologist:
-
Employment Type:
Contractor
-
Location:
New Jersey, US (Onsite)
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Pharmacoepidemiologist
Careers Integrated Resources Inc
New Jersey, US (Onsite)
Contractor
Pay rate: $66.93- $89.23
Job Description: Job Title: Pharmacoepidemiologist
Location: 100% remote
Work Schedule: Mon Fri 8:00am to 5:00pm
Purpose and Product of the Position:
We are seeking a highly motivated epidemiologist to be part of the Patient Safety organization. The successful candidate will be responsible for providing assistance in Epidemiology's role to support the cross-functional Safety Management Teams (SMT). She/he will be expected to work on post-marketing requirements (PMR/Client) as well as assist in the signal detection and management processes.
Duties and Responsibilities:
Managing post-marketing studies (PMR/Client) in the execution and reporting phases.
Participating in planning and preparing strategic regulatory aggregate reports (e.g. Risk Management Plan, Periodic Benefit-Risk Evaluation Report, Product Label Updates).
Supporting Medical Safety Assessment Physicians (MSAP) in leading and coordinating individual cross-functional Medical Surveillance Teams (SMTs) and assigned sub-teams, such as Safety Data Review (SDR) Teams.
Participating in the development of materials regarding issues impacting key SMT activities, milestones, or documents.
Executing searches of the worldwide literature and other data sources, applying critical thinking and independent research skills to ensure the information is appropriate and usable.
Assisting in safety surveillance and signal detection for products across therapeutic areas.
Leading, planning, organizing, and forecasting requirements and/or resources based on Book of Work and other upcoming tasks and activities for assigned product portfolio.
Executing searches of the corporate safety database, J-review database, and the worldwide literature, applying critical thinking and independent research skills to ensure the information is appropriate and usable.
Applying medical, life science and general scientific knowledge and expertise to create and manage plans and budgets for designated projects.
Education:
Master s Degree in Related Field(s) plus 5+ years of experience
OR
PhD with 3 years of experience
Experience:
Experience in observational study design.
Experience working with regulatory submissions to heath authorities.
Data Analysis using SAS/R.
Working in a leading role within a metrics team.
Working Conditions: No exposure to hazards or disagreeable conditions.
Travel required: None
Physical Demands: None
Job Description: Job Title: Pharmacoepidemiologist
Location: 100% remote
Work Schedule: Mon Fri 8:00am to 5:00pm
Purpose and Product of the Position:
We are seeking a highly motivated epidemiologist to be part of the Patient Safety organization. The successful candidate will be responsible for providing assistance in Epidemiology's role to support the cross-functional Safety Management Teams (SMT). She/he will be expected to work on post-marketing requirements (PMR/Client) as well as assist in the signal detection and management processes.
Duties and Responsibilities:
Managing post-marketing studies (PMR/Client) in the execution and reporting phases.
Participating in planning and preparing strategic regulatory aggregate reports (e.g. Risk Management Plan, Periodic Benefit-Risk Evaluation Report, Product Label Updates).
Supporting Medical Safety Assessment Physicians (MSAP) in leading and coordinating individual cross-functional Medical Surveillance Teams (SMTs) and assigned sub-teams, such as Safety Data Review (SDR) Teams.
Participating in the development of materials regarding issues impacting key SMT activities, milestones, or documents.
Executing searches of the worldwide literature and other data sources, applying critical thinking and independent research skills to ensure the information is appropriate and usable.
Assisting in safety surveillance and signal detection for products across therapeutic areas.
Leading, planning, organizing, and forecasting requirements and/or resources based on Book of Work and other upcoming tasks and activities for assigned product portfolio.
Executing searches of the corporate safety database, J-review database, and the worldwide literature, applying critical thinking and independent research skills to ensure the information is appropriate and usable.
Applying medical, life science and general scientific knowledge and expertise to create and manage plans and budgets for designated projects.
Education:
Master s Degree in Related Field(s) plus 5+ years of experience
OR
PhD with 3 years of experience
Experience:
Experience in observational study design.
Experience working with regulatory submissions to heath authorities.
Data Analysis using SAS/R.
Working in a leading role within a metrics team.
Working Conditions: No exposure to hazards or disagreeable conditions.
Travel required: None
Physical Demands: None
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