Associate Director, Study Management

Scorpion Therapeutics

Philadelphia (Philadelphia County)

Hybrid

USD 180,000 - 250,000

Full time

8 days ago

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Job summary

Scorpion Therapeutics is seeking a Senior Clinical Operations Leader to drive the operational strategy for global clinical programs. The role partners with cross-functional teams to align resources, budgets, and timelines with the Clinical Development Plan, while chairing trial leadership activities as needed.

You will develop trial strategies, manage program-level planning, and lead risk mitigation, ensuring governance-ready operations and strong collaboration across Finance, Quality, Data

Qualifications

  • BS/BA required; 8+ years clinical research/operational experience.
  • 8+ years global trial experience (Phase 1–4) with 3+ leading end-to-end trials, including Phase 3.
  • 2–5 years people leadership experience.
  • Knowledge of pharmaceutical development processes.
  • Strong decision-making, analytical, and financial management skills.

Responsibilities

  • Accountable for delivery of operational strategy aligned with the Clinical Development Plan, including resourcing, budget, and change control; partner with CTWG and CDST on timeline creation.
  • May chair and/or support Trial Leader in leading CTWG for execution of assigned trials.
  • Develop and execute trial operational strategies and contribute to program-level planning with Director and cross-functional stakeholders.
  • Lead operational scenario planning; mitigate risks impacting timelines/budget.
  • Provide timely/quality oversight; escalation issues to Director, Quality, and functional leadership.

Skills

Leadership
Project management
Financial management
Analytical skills
Communication
MS Office

Education

BS/BA

Tools

MS Project
Excel
PowerPoint

Job description

Summary of Key Responsibilities
  • Accountable for delivery of operational strategy aligned with the Clinical Development Plan, including resourcing, budget, and change control; partner with CTWG and CDST on timeline creation.
  • May chair and/or support Trial Leader in leading CTWG for execution of assigned trials.
  • Develop and execute trial operational strategies and contribute to program-level planning with Director and cross-functional stakeholders.
  • Lead operational scenario planning; mitigate risks impacting timelines/budget.
  • Provide timely/quality oversight; escalation issues to Director, Quality, and functional leadership.
  • Communicate and defend operational plan and costs at governance meetings as appropriate.
  • Lead inspection readiness; build a knowledgeable, skilled clinical operations team.
  • Promote cross-functional collaboration; set goals aligned with company/program/department goals.
  • Ensure staff training; develop team performance through coaching and guidance.
  • Represent Clinical Operations at CDST for early development programs.
  • Interface with key internal stakeholders (e.g., Finance, Program/Vendor Management, Safety, Quality Assurance, Data Mgmt, Statistics, Regulatory, etc.).
  • Lead/participate in process improvements; support Health Authority inspections and internal QA audits.
  • Ability to travel ~10% average.
Qualifications
  • BS/BA required.
  • 8+ years clinical research experience (CRO/biotech/pharma) on Phase 1–4 global trials; at least 3 leading end‑to‑end global trials, including Phase 3 registrational trials.
  • 2–5 years people leadership experience.
  • Knowledge of pharmaceutical development process.
  • Strong decision‑making, analytical, and financial management skills; ability to manage all clinical trial execution aspects.
  • Leadership, ability to foster productivity with limited supervision; leading without authority in matrix/global environments.
  • Strong project planning, written/verbal communication, presentation, organizational, and problem‑solving skills.
  • Apply project management best practices; experience in novel clinical drug development.
  • Proficient: MS Office (Excel, Word, PowerPoint) and MS Project.
Hybrid/Location
  • Hybrid role, preferably Cambridge, MA or Philadelphia, PA (remote for exceptional candidates).
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