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Clinical Scientist, Clinical Development
Spyre Therapeutics. Design, execute and interpret clinical trials supporting development of novel antibody-based therapies .
Posted 11/10/2026full-timeRemote • United StatesMid-LevelSenior💰 $175,000 - $205,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in designing and executing clinical trials, particularly in immunology and IBD, while ensuring compliance with FDA/ICH guidelines and Good Clinical Practice (GCP). Strong ability to collaborate cross-functionally and communicate effectively with diverse stakeholders.
Highest-signal resume keywords
Clinical Trial DesignImmunology ExperienceFDA/ICH ComplianceCross-Functional CollaborationClinical Data Review
ATS Keywords
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Hard Skills
Clinical Trial ExecutionProtocol DevelopmentData AnalysisBiomarker UnderstandingPK/PD ModellingAdverse Event ReviewRegulatory Submission WritingStudy DesignRisk-Based Quality OversightPatient Safety Monitoring
Soft Skills
Excellent CommunicationInterpersonal SkillsInfluencing StakeholdersAdaptabilityTeam Collaboration
Industry Keywords
BiotechPharmaImmunologyGastroenterologyIBDClinical DevelopmentGood Clinical PracticeClinical PharmacologyTherapeutics LandscapeClinical Documentation
About the role
Key responsibilities & impact- Design, execute and interpret clinical trials supporting development of novel antibody-based therapies
- Collaborate with clinical operations, data management, CROs, regulatory, translational science and biomarker teams
- Review clinical trial data to identify trends, clean discrepancies and ensure patient safety and protocol compliance
- Review adverse events, laboratory data, concomitant medications, medical histories and clinical data queries
- Assist with Medical Monitor responsibilities
- Contribute to study design and protocol amendments
- Author and support submission of protocols, regulatory filings and related documentation
- Support site selection, study start-up, trial metric monitoring, risk-based quality oversight and study close-out
- Write and review abstracts, posters, scientific meeting content, presentations and publicly distributed materials
- Write clinical science sections of meeting packages and support clinical documentation for regulatory submissions
- Collaborate with Regulatory Affairs to ensure FDA/ICH and GCP-aligned study designs
- Develop and maintain protocols, clinical study reports, investigator brochures and informed-consent forms
- Monitor the competitive and scientific therapeutics landscape and contribute to strategic positioning of pipeline programs
- Perform additional duties as assigned
Requirements
What you’ll need- 5+ years of clinical development experience in the biotech/pharma industry
- Ideally, at least 2 years in immunology, gastroenterology/IBD or immune-mediated disease area
- Bachelor's degree in life sciences, clinical pharmacology, immunology or related discipline
- Demonstrated experience executing clinical trials in IBD or another I&I therapeutic area
- Understanding of clinical biomarkers, PK/PD modelling, patient stratification and immunologic endpoints
- Familiarity with FDA/ICH guidelines and Good Clinical Practice (GCP)
- Proven ability to work cross-functionally in a matrix organization
- Excellent written and verbal communication, presentation and interpersonal skills
- Ability to influence diverse stakeholders
- Comfortable working in a fast-paced, dynamic environment with ambiguity and willing to wear multiple hats
Benefits
Comp & perks- Market competitive compensation and benefits package
- Performance bonus
- Equity grant opportunities
- Health benefits
- Welfare benefits
- Retirement benefits
- Unlimited PTO
- Two, one-week company-wide shutdowns each
- Professional development opportunities
- Remote working environment with frequent in-person meetings
- Opportunity to work in a fast-paced, dynamic environment, contribute broadly to advance meaningful medicines, and learn quickly