Senior Epidemiologist

LeadStack Inc.; Foster City (CA); On-site; USD 125,000 - 150,000; Full time

Job summary

An established industry player is seeking a skilled Epidemiologist to join their dynamic team for a 12-month contract. This role involves conducting feasibility analyses, planning and drafting observational studies, and ensuring high-quality data analysis. You will collaborate with various stakeholders, adapting priorities to meet study milestones while maintaining data integrity. If you have a passion for research and a strong background in epidemiology, this opportunity offers a chance to make a significant impact in the pharmaceutical and biotechnology sectors. Join a forward-thinking company where your expertise will be valued and your contributions will shape the future of healthcare.

Qualifications

• 7-10 years of experience as an epidemiologist in the industry.
• Oncology and safety RWE/RWD experience preferred.

Responsibilities

• Conduct feasibility analysis and plan observational studies.
• Draft and review observational study protocols and reports.
• Collaborate with stakeholders to ensure timely completion of studies.

Skills

Feasibility Analysis

Protocol Drafting

Statistical Analysis

Data Quality Review

Collaboration

Education

Master's or Doctorate in Epidemiology

Job description

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

Base pay range

$90.00/hr - $135.00/hr

Job Title: Epidemiologist

Location: Foster City, CA

Duration: 12 Months

PR: $100/hr - $135/hr on W2

Responsibilities

1. Perform feasibility analysis for studies
2. Plan observational studies and draft protocol synopsis (or protocol concept sheet)
3. Determine observational study design criteria – including source data, analytical methods and analysis plans
4. Draft and review observational study protocols
5. Draft and review observational study analysis specifications, including statistical analysis plans (SAPs)
6. Draft and review observational study reports
7. Conduct observational studies, both primary data collection and secondary data use studies
8. Review analysis outputs for quality, including study analysis, ad hoc analysis, analysis to support conference or publications
9. Conduct quality review of all deliverables to ensure data and results are accurate
10. Work with scientific and operational stakeholders to identify and resolve issues
11. Collaborate with study teams, vendors and other stakeholders to advance study and analysis deliverables
12. Work with relevant stakeholders to meet study milestones and timelines
13. Participate in program or study planning meetings
14. Actively adapt and adjust priorities to ensure timely and quality completion of assigned tasks
15. Perform other related duties as required by the Department.

Experience

1. (7 – 10)+ years industry experience as an epidemiologist
2. Oncology and safety RWE/RWD experience preferred

Seniority level

Mid-Senior level

Employment type

Contract

Job function

Research, Analyst, and Information Technology

Industries

Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing