Associate Director, Clinical Scientist

Deciphera Pharmaceuticals

. Lead ongoing clinical data review to support data quality, interpretation, and patient safety .

Posted 11/3/2026full-timeRemote • Massachusetts • United StatesSenior💰 $193,000 - $230,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical data review, analysis, and interpretation, with a strong focus on patient safety and data quality. Proven ability to collaborate cross-functionally and communicate complex scientific information effectively.

Highest-signal resume keywords

Clinical Data ReviewClinical Development ExperienceCross-Functional CollaborationPresentation SkillsPharmaceutical Industry Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data AnalysisClinical Trial Data InterpretationStudy Protocol ReviewEDC DevelopmentBiostatistics CollaborationRegulatory Document ReviewClinical Document PreparationOncology Clinical DevelopmentNeurology Clinical DevelopmentRare Disease Experience

Soft Skills

Organizational SkillsCommunication SkillsIndependent Work Ability

Certifications & Qualifications

PhD or Equivalent DegreeBachelor's/Master's Degree

Industry Keywords

Clinical ScientistPhase I–III Clinical DevelopmentPharmaceutical IndustryClinical Drug DevelopmentBiologics Development

About the role

Key responsibilities & impact

Lead ongoing clinical data review to support data quality, interpretation, and patient safety
Identify and escalate clinically relevant findings and partner with study teams to resolve data-related issues
Collaborate with Data Management and Clinical Operations on study implementation and EDC development
Contribute to and review clinical documents, including study protocols, investigator brochures, regulatory documents, and concept materials
Review and interpret clinical study data and outputs with Biostatistics, Pharmacovigilance, and other stakeholders
Represent Clinical Development on cross-functional study teams
Work closely with Medical Directors and functional partners
Prepare and present clinical data, study designs, and scientific information to study teams, investigator meetings, advisory boards, study committees, and other audiences
Perform other duties and responsibilities as assigned

Requirements

What you’ll need

PhD or equivalent degree with 2+ years of relevant experience, or bachelor’s/master’s degree with 5+ years of relevant post-graduate experience
Pharmaceutical industry experience in clinical drug or biologics development
Experience as a Clinical Scientist or in a comparable clinical development role
Ability to work independently
Hands-on experience reviewing, analyzing, and interpreting clinical trial data
Strong cross-functional collaboration, organizational, communication, and presentation skills
Experience supporting Phase I–III clinical development programs preferred
Clinical development experience in oncology and/or neurology preferred
Rare disease experience preferred
Up to 20% business travel may be required

Benefits

Comp & perks

Annual performance bonus
Long-term incentive plan
Comprehensive benefits package including medical, dental, and vision insurance
401(k) retirement plan with company match
Generous parental leave and family planning benefits
Opportunities for personal and professional growth
Flexible hybrid or remote work arrangement within approved U.S. working locations