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Associate Principal Scientist, Clinical Research

Job in Pittsburgh, Allegheny County, Pennsylvania, 15289, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-07-09
Job specializations:
  • Research/Development
    Clinical Research
Salary/Wage Range or Industry Benchmark: 142400 - 224100 USD Yearly USD 142400.00 224100.00 YEAR
Job Description & How to Apply Below

Early Clinical Scientist (ECS)
Responsibilities

  • Provide operational and scientific leadership for early-phase clinical trial design, planning, and execution in collaboration with Clinical Director and cross-functional teams.
  • Oversee and execute Immunology programs (multiple Phase 1 and 1b trials), manage cross‑functional performance to meet objectives, and ensure GCP/ICH/regulatory compliance.
  • Conduct clinical safety assessment and real‑time oversight of ongoing trials; review and interpret trial data and support site monitoring and training for novel endpoint/biomarker collection.
  • Represent Early Stage Development on product and early development teams; lead departmental job aids/SOPs; develop and promote global clinical procedures; coach and mentor junior staff.
  • Author and coordinate clinical/regulatory documents (protocols, investigator brochures, study reports, health authority updates, regulatory/audit responses; WMA/CTD subsections); develop study operational documents.
  • Lead study and program project management (planning, issue escalation and mitigation, governance/advisory preparation) with risk assessments and contingency planning.
Qualifications
  • Degree in Life Sciences.
  • Bachelor’s + ≥11 years related experience, OR Master’s + ≥8 years, OR PhD/doctorate + ≥3 years (e.g., trial management/execution, clinical site training/monitoring, medical/regulatory writing).
Required
  • ≥6 years early‑phase/translational medicine clinical research; immunology clinical program/trial experience (including early patient trials such as Phase 1b in rheumatology, dermatology, gastroenterology) under accelerated timelines.
  • Strong clinical research execution, scientific/medical/safety writing, data‑driven decision‑making, and independent judgment on regulations and investigator interactions.
  • Working knowledge of GCP/ICH/regulatory requirements; effective communication; ability to mentor.
Preferred
  • Advanced degree.
  • Global Phase 1 patient trials and safety reporting.
  • NDA/WMA submission experience.
Benefits/Compensation

Salary range: $–$; bonus and long‑term incentive eligibility (if applicable); comprehensive medical, dental, and vision coverage, retirement (401(k)), and paid time off.

Application

Apply via  (or Workday Jobs Hub for current employees). Apply by the deadline stated on the posting.

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Position Requirements
10+ Years work experience
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