Epidemiologist

Orion Group; United States; Remote; Full time

Job summary

Orion Group seeks a Clinical Application Specialist I in Epidemiology to support the Global Epidemiology group within a prominent pharmaceutical context. This role involves designing and executing pharmacoepidemiologic studies, contributing to regulatory submissions, and producing literature reviews. Ideal candidates will hold an MPH, MS, or PhD in a related field, with SAS experience being crucial. This position is remote with a contract duration of over 6 months and offers a competitive hourly rate.

Benefits

Medical insurance

Vision insurance

401(k)

Qualifications

• 2+ years experience in epidemiology or outcomes research.
• Excellent understanding of epidemiologic methods.
• Experience with disease epidemiology globally.

Responsibilities

• Evaluate and communicate epidemiology literature.
• Lead evidence development through study design.
• Generate and review validated outputs for clinical projects.

Skills

Epidemiologic data sources

Statistical analysis

SAS programming

Education

MPH or MS in Epidemiology or related discipline

PhD/MD/PharmD with experience

Job description

This range is provided by Orion Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$47.00/hr - $50.00/hr

Direct message the job poster from Orion Group

Clinical Application Specialist I – Epidemiology

6+ month initial contract

Remote

Hourly Pay Rate: $47-50/hr (individual medical benefits available at a cost)

Job Description:

Orion Group has partnered with our global pharmaceutical client for an exciting opportunity in the field of Epidemiology. We are seeking to hire a Clinical Application Specialist who will provide support to the Global Epidemiology group in the Clinical Sciences division. This person will contribute to the design and execution of pharmacoepidemiologic studies, support characterization of descriptive epidemiology for diseases and indications, contribute to regulatory submissions and responses, and perform literature reviews on topics required for ongoing support and/or development of drugs and devices.

Responsibilities:

• Evaluate, synthesize, and communicate epidemiology literature in both written and presentation formats
• Lead or contribute to the development of new evidence through study design, protocol development, and statistical analysis plans of various databases, including secondary data sources, such as administrative claims or health records data
• Support departmental need to contribute to and develop content for sections of risk management plans, benefit risk assessments, safety and regulatory deliverables
• Understands the role of epidemiology in signal evaluation and where epidemiology contributes to key safety and regulatory deliverables.
• Generate tables, listings, and graphs for a compound project.
• Responsible for participating in the validation and quality assurance of any output produced.
• Generate and review validated table, listing and graph output meeting the needs of clinical projects.

Required Experience:

• MPH or MS with more than 2 years of experience or PhD/MD/PharmD with experience in the field of epidemiology, outcomes research, or related discipline.
• Excellent understanding of epidemiologic data sources and methods and a demonstrated ability to apply them to address program needs
• Experience with disease epidemiology (population sizing) globally and regionally using short-term studies/analyses
• Preference given to individuals with industry experience & clinical experience
• SAS program experience required.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Research

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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