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Director, Clinical Scientist – Respiratory Indications
Generate Biomedicines. Serve as clinical science lead and core member of clinical development teams for respiratory studies .
Posted 9/28/2026full-timeRemote • Massachusetts • United StatesLead💰 $186,000 - $270,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial design, execution, and regulatory compliance, particularly in late-stage respiratory studies. Proven ability to lead cross-functional teams and mentor colleagues while ensuring data quality and participant safety.
Highest-signal resume keywords
Clinical Trial DesignRegulatory ComplianceLate-Stage Respiratory StudiesClinical Research MethodologiesCross-Functional Collaboration
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Protocol DevelopmentRegulatory Document AuthoringData Quality ReviewRisk AssessmentStudy Progress Tracking
Soft Skills
Analytical SkillsCommunication SkillsMentoringCollaboration
Certifications & Qualifications
PhDPharmDMDMSPMP
Industry Keywords
Clinical DevelopmentGCPCRO ManagementAsthma StudiesCOPD Studies
Tech Stack
Tools & technologiesGoogle Cloud PlatformPMP
About the role
Key responsibilities & impact- Serve as clinical science lead and core member of clinical development teams for respiratory studies
- Support day-to-day study execution and alignment with protocols, timelines, and regulatory requirements
- Design and develop clinical trial protocols and associated documents
- Develop clinical components of regulatory documents
- Review and interpret clinical data to ensure data quality, participant safety, and protocol compliance
- Participate in site selection, initiation, and ongoing engagement
- Track study progress, identify risks, and implement mitigation strategies
- Serve as scientific contact for CROs and vendors
- Collaborate with Clinical Operations, Regulatory, Biostatistics, Data Management, and Safety teams
- Contribute to governance meetings, study updates, data summaries, and risk assessments
- Maintain inspection readiness and support audits and inspections
- Support publications, abstracts, and manuscripts
- Contribute to TPPs, clinical development plans, and risk-benefit assessments
- Support oversight committees for late-stage asthma studies
- Mentor and coach team members where appropriate
Requirements
What you’ll need- Advanced degree (PhD, PharmD, MD, MS, PMP)
- 9+ years of industry experience in clinical development
- Direct experience in late-stage respiratory (asthma and/or COPD) studies
- Strong knowledge of clinical research methodologies, regulatory guidelines, and GCP
- Demonstrated ability to lead clinical science strategy and execution in late-stage trials
- Excellent analytical, communication, and cross-functional collaboration skills
- Prior experience authoring clinical protocols, CSRs, and regulatory documents
Benefits
Comp & perks- Annual bonus
- Equity compensation
- Competitive benefits package
- Remote work option in the U.S. with travel to HQ based on business needs