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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
Job Title: Pharmacoepidemiologist
Job Location: Remote, NJ
Job Duration: 6 Months (possibility of extension)
Shift: Mon – Fri 8:00am to 5:00pm
Payrate: $66.93 - $89.23/ hr on w2
Job Summary:
Job Location: Remote, NJ
Job Duration: 6 Months (possibility of extension)
Shift: Mon – Fri 8:00am to 5:00pm
Payrate: $66.93 - $89.23/ hr on w2
Job Summary:
- 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.
- 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.
- Master’s Degree in Related Field(s) plus 5+ years of experience. PhD with 3 years of 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.
- No exposure to hazards or disagreeable conditions.
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