Remote Epidemiologist: Regulatory & Vaccine Safety

Kaiva Corp; Washington (District of Columbia); On-site; USD 110,000 - 140,000; Full time

Job summary

Kaiva Corp is seeking an experienced Epidemiologist (Mid) to provide scientific and regulatory support for vaccines and related products in a remote capacity. The role emphasizes pharmacoepidemiology, data interpretation, and clear scientific communication for government stakeholders.

The candidate will review regulatory submissions, contribute to briefing materials, and help prepare manuscripts and technical reports while ensuring compliance with applicable laws and FDA guidelines.

Qualifications

• Minimum seven years conducting pharmacoepidemiology studies using large datasets.
• Experience supporting regulatory review activities for vaccines/biologics.
• Ability to synthesize regulatory or public health information for diverse audiences.
• Experience leading multiple time-sensitive projects with stakeholders.

Responsibilities

• Support regulatory review of vaccines and related biological products.
• Prepare, edit, and quality-review regulatory and scientific documents.
• Review epidemiologic data from real-world sources (claims, EHRs, registries).
• Synthesize complex information into clear conclusions for technical and non-technical audiences.
• Collaborate with government stakeholders to prioritize assignments and timelines.
• Ensure compliance with relevant laws, policies, and accessibility requirements.

Skills

Pharmacoepidemiology

Regulatory science

Scientific writing

Project management

Data interpretation

Education

Post-Doctoral Degree in Epidemiology

Job description

Kaiva Corp is seeking an experienced Epidemiologist (Mid) to provide scientific and regulatory support for vaccines and related products in a remote capacity. The role emphasizes pharmacoepidemiology, data interpretation, and clear scientific communication for government stakeholders.

The candidate will review regulatory submissions, contribute to briefing materials, and help prepare manuscripts and technical reports while ensuring compliance with applicable laws and FDA guidelines.