Clinical Scientist Associate Director – Early Development Inflammation
$192,597–$260,572 year
RemoteUnited States
Job Summary
Support Inflammation early clinical development by contributing to protocol development, study start-up, and data review activities. Collaborate with study teams to ensure high-quality, decision-ready clinical data through cross-functional coordination and problem management. Author clinical protocols, Investigators Brochures, and regulatory documents while overseeing data management plans and CRF design. Manage collaborators and Clinical Research Organizations, then support review, analysis, and presentation of trial data for internal decisions and regulatory submissions. Anticipate and resolve problems across teams to translate clinical strategy into study concepts.
Required Qualifications
- Doctorate degree
- Master's degree
- Bachelor's degree
- Associate's degree
- High school diploma / GED
- 3 years of clinical development experience
- 5 years of clinical development experience
- 7 years of clinical development experience
- 12 years of clinical development experience
- 14 years of clinical development experience
Desired Qualifications
- 3 years of experience in a pharmaceutical industry setting
- at least 1 year supporting early or late-phase clinical development within a relevant therapeutic area or disease indication
- Demonstrated experience contributing to clinical trial process improvements within a therapeutic area or study team environment
- Strong communication and presentation skills, with the ability to clearly convey scientific concepts and clinical data to cross-functional teams and leadership audiences, both written and oral
- Experience supporting the design, monitoring, and implementation of clinical trials in compliance with Good Clinical Practice standards and applicable regulatory requirements
- Working knowledge of study data readout activities, including data cleaning, database lock, data extraction, and generation of clinical data outputs
- Experience contributing to regulatory submission documents and supporting clinical regulatory responses for health authority interactions under guidance
- Experience serving as a contributing author on scientific publications or data presentations for internal forums or scientific conferences
- Experience in clinical data analysis such as Spotfire or other data analysis tools
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