Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Lifelancer

Senior Advisor, Clinical Science

Lifelancer

. Serve as clinical scientist on one or more late-stage (Phase 2-3) global clinical trials for Orexin-targeted sleep/wake programs .

Posted 10/17/2026full-timeRemote • United StatesSenior💰 $153,000 - $268,400 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial design and drug development, with a strong foundation in neuroscience and the ability to author and review critical clinical documents. Proven track record of cross-functional collaboration and effective communication in a fast-paced biotech environment.

Highest-signal resume keywords
Clinical Trial DesignClinical Data AnalysisDrug Development PrinciplesClinical Document AuthoringNeuroscience Expertise

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Study Report AuthoringProtocol DevelopmentInvestigator Brochure CreationSafety Data ReviewEnrollment MonitoringCRF DesignStatistical Analysis Plan DevelopmentData Integrity AssessmentRegulatory Document ReviewScientific Presentation Preparation
Soft Skills
Effective CommunicationOrganizational SkillsProblem-SolvingCross-Functional CollaborationDetail Oriented
Certifications & Qualifications
PhDPharmD
Industry Keywords
BiotechPharmaOrexin BiologyNeurocircuitry MechanismsClinical OperationsPharmacovigilanceStudy ManagementGlobal Clinical TrialsInvestigator MeetingsAdvisory Boards

About the role

Key responsibilities & impact
  • Serve as clinical scientist on one or more late-stage (Phase 2-3) global clinical trials for Orexin-targeted sleep/wake programs
  • Support creation and review of clinical slides for investigator meetings, SIVs, IDMCs, advisory boards, and other meetings
  • Author or review protocols, Clinical Study Reports, Investigator Brochures, Development Safety Update Reports, and other study documents
  • Serve as study scientific expert from startup through Clinical Study Report completion
  • Support CRF design, enrollment monitoring, and patient profile review
  • Liaise with Clinical Operations on site selection, startup, study management, and closeout
  • Serve as primary contact for clinical inquiries from sites, CROs, site monitors, and health authorities
  • Integrate clinical and regulatory strategy into global product development strategy
  • Review clinical data for safety, data integrity, protocol compliance, and study performance
  • Lead cross-functional collaboration with Clinical Operations, Regulatory Affairs, Biostatistics, and Safety/Pharmacovigilance
  • Identify and address scientific, operational, and strategic risks and gaps
  • Develop scientific insights and recommendations for clinical development decisions
  • Partner with biostatistics on SAP development and review and interpretation of final clinical study TLFs
  • Support abstracts, posters, manuscripts, and scientific presentations
  • Provide scientific leadership with investigators, CROs, vendors, external experts, key opinion leaders, and scientific advisory boards
  • Manage deliverables across assigned studies and workstreams

Requirements

What you’ll need
  • Advanced scientific/clinical degree (PhD or PharmD) with 2+ years drug development experience in the biotech/pharma industry, OR BS/MS in a scientific discipline with 8+ years drug development experience in the biotech/pharma industry
  • Strong scientific foundation in neuroscience/neurology
  • Understanding of clinical trial design, clinical data analysis, and drug development principles
  • Demonstrated accountability for delivery on clinical studies
  • Proven experience developing and authoring clinical and regulatory documents, including protocols, IBs, CSRs, and briefing documents
  • Familiarity with Orexin biology or related sleep/wake and neurocircuitry mechanisms preferred
  • Detail oriented with exceptional organizational skills
  • Effective verbal and written communication skills
  • Ability to identify issues, analyze situations, and provide effective solutions
  • Ability to partner with cross-functional teams in a fast-paced biotech environment
  • Role based in the United States
  • Occasional travel

Benefits

Comp & perks
  • Company bonus based partly on company and individual performance
  • Company-sponsored 401(k)
  • Pension
  • Vacation benefits
  • Medical, dental, vision, and prescription drug benefits
  • Healthcare and/or dependent day care flexible spending accounts
  • Life insurance and death benefits
  • Time off and leave of absence benefits
  • Employee assistance program
  • Fitness benefits
  • Employee clubs and activities
  • Remote work with occasional travel