Remote SME: Regulatory & Scientific Training Designer

Team Carney, Inc.

Silver Spring (MD)

On-site

USD 120,000 - 160,000

Full time

11 days ago
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Benefits offered by this job

Health insurance
Dental & Vision coverage
401(k) plan with company match
Paid time off and holidays
Tuition assistance

Job summary

Team Carney is seeking a Subject Matter Expert – Regulatory / Scientific to validate, design, and enrich highly specialized training curricula for FDA regulatory reviewers and scientific personnel. This role supports the development of robust, compliant content across complex regulatory scenarios.

This remote position requires periodic on-site presence at Silver Spring, MD and a seven-plus year background in regulatory, scientific, or technical roles, plus an advanced degree.

Qualifications

  • Minimum of seven (7) years of professional experience in a regulatory, scientific, or technical role.
  • Advanced degree (Master’s or Ph.D.) in a relevant field required.
  • Deep understanding of regulatory review processes, decision-making frameworks, scientific evaluation standards, and regulatory documentation practices.
  • Proven experience collaborating with instructional design teams to review, validate, and co-develop courseware, case studies, and practical exercises.
  • Familiarity with continuing education (CE), professional credentialing, and accreditation alignment preferred.

Responsibilities

  • Validate, design, and enrich training curricula for FDA regulatory reviewers and scientific personnel.
  • Translate complex regulatory review frameworks into practical case studies, simulations, and role-based training modules.
  • Collaborate with Instructional Systems Designers to ensure technical accuracy and regulatory defense of training content.

Skills

Regulatory expertise
Curriculum development
Scientific evaluation
Regulatory documentation

Education

Advanced degree (Master’s/Ph.D.)

Job description

Team Carney is seeking a Subject Matter Expert – Regulatory / Scientific to validate, design, and enrich highly specialized training curricula for FDA regulatory reviewers and scientific personnel. This role supports the development of robust, compliant content across complex regulatory scenarios.

This remote position requires periodic on-site presence at Silver Spring, MD and a seven-plus year background in regulatory, scientific, or technical roles, plus an advanced degree.

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