Senior Regulatory Scientific Advisor

Evolution Research Group

. Provide senior-level regulatory and scientific guidance on FDA guidance and regulatory requirements as they apply to clinical research .

Posted 11/4/2026part-timeRemote • United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive expertise in clinical research and regulatory affairs, with a strong focus on FDA guidance, clinical trial design, and data analysis. Capable of providing senior-level scientific guidance and maintaining compliance with regulatory standards.

Highest-signal resume keywords

Medical Degree (MD) or Equivalent Advanced Scientific DegreeExtensive Senior-Level Experience in Clinical ResearchDemonstrated Experience with FDA GuidanceStrong Background in Clinical Trial DesignAbility to Maintain Confidentiality

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchRegulatory AffairsClinical Trial DesignData AnalysisClinical ReviewsProtocol DevelopmentGCP TrainingHIPAA ComplianceRegulatory StandardsEvaluation of Development Opportunities

Soft Skills

Sound JudgmentDiscretionIndependent WorkCommunication Skills

Industry Keywords

FDA GuidanceClinical TrialsScientific LeadershipConfidentialityComplianceSOP Training

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Provide senior-level regulatory and scientific guidance on FDA guidance and regulatory requirements as they apply to clinical research
Perform clinical reviews and advise on findings
Advise on clinical trial design, including protocol development and review, trial conduct, and analysis of trial data
Offer scientific opinions on development programs and the impact of regulatory expectations
Participate in Scientific Leadership Team meetings, generally Mondays and Wednesdays from 4:00–5:00 pm Eastern Time
Review meeting agendas, topics, protocols, and related materials in advance
Learn about new opportunities under consideration and provide opinions
Request involvement in projects where the company is open to it
Agree in advance with company leadership on anticipated hours for specified advisory work
Take on special projects only when discussed and approved in advance
Maintain confidentiality of company materials, information, and business plans
Perform other duties supporting clinical research and development activities

Requirements

What you’ll need

Medical degree (MD) or equivalent advanced scientific degree required
Extensive senior-level experience in clinical research and regulatory affairs required
Demonstrated experience with FDA guidance and clinical reviews required
Strong background in clinical trial design, conduct, and data analysis required
Experience evaluating new development opportunities and communicating clear, practical opinions to executive and scientific leadership preferred
Ability to complete required training, including GCP, HIPAA, and company SOP training
Ability to work independently and remotely, with availability for Monday and Wednesday afternoon meetings when possible
Sound judgment and discretion in handling confidential and proprietary information
Successful completion of a background check and drug screening
Signed non-disclosure and at-will employment agreements
Maintain compliance with company policies, HIPAA requirements, and applicable regulatory standards

Benefits

Comp & perks

PRN position with a baseline commitment of approximately 5 hours per week
Remote work from a home-office setting
Company-provided or standard office equipment, including computer, telephone, video conferencing, and internet access