Director, Clinical Scientist (Respiratory indications)

Added
3 hours ago
Type
Full time
Salary
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Related skills

gcp regulatory submissions clinical development protocol development csrs
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๐Ÿ“‹ Description

  • Lead clinical science on respiratory studies (asthma/COPD) for Phase 2/3 trials.
  • Drive protocol development, data analysis, and regulatory documentation.
  • Collaborate across Clinical Development, Regulatory, Biostatistics, Data Management, and Safety.
  • Oversee medical monitoring, data quality, patient safety, and protocol compliance.
  • Support investigator site engagement, CROs, and vendor oversight with scientific input.
  • Contribute to study governance, publication plans, and risk assessments.

๐ŸŽฏ Requirements

  • Advanced degree (PhD, PharmD, MD, MS, PMP) with 9+ years in industry clinical development.
  • Expertise in late-stage respiratory studies and trial design/execution.
  • Strong knowledge of clinical research methodologies, regulatory guidelines, and GCP.
  • Proven ability to lead clinical science strategy and execution in late-stage trials.
  • Excellent analytical, communication, and cross-functional collaboration skills.
  • Experience authoring clinical protocols, CSRs, and regulatory documents.

๐ŸŽ Benefits

  • Annual bonus, equity compensation, and competitive benefits package.
  • Opportunity to contribute to groundbreaking AI-driven biology programs.
  • Remote work with occasional travel to HQ as needed.
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