[Hiring] Senior Clinical Project Manager @Deciphera Pharmaceuticals

Role Description

The Senior Clinical Project Manager leads the execution of complex global clinical studies, providing hands-on operational leadership across study teams and external partners. This role is responsible for driving study execution, managing timelines and budgets, and ensuring trials are delivered with quality and in compliance with applicable requirements.

The ideal candidate brings strong later-stage clinical trial experience, ideally including Phase III, and is comfortable taking ownership, working through challenges, and knowing when to engage others for support.

Key Responsibilities

• Clinical Trial Leadership & Execution:
  • Lead the planning, execution, and delivery of assigned global clinical studies, with responsibility for timelines, budgets, quality, and overall operational execution.
  • Identify and address operational risks and challenges to keep studies on track.
• Cross-Functional Leadership:
  • Lead cross-functional study teams, driving collaboration, accountability, decision-making, and problem-solving.
  • Partner across Clinical Operations, Data Management, Regulatory, Clinical Supply, and other functions to support global study execution.
• CRO & Vendor Management:
  • Oversee CROs and external vendors, monitoring performance and ensuring alignment with study timelines, budgets, quality expectations, and contractual obligations.
• Stakeholder Communication & Operational Excellence:
  • Communicate study progress, risks, and key decisions clearly to internal stakeholders and Clinical Operations leadership.
  • Contribute to Clinical Operations processes and ways of working that support efficient, high-quality study execution.
• Other duties and responsibilities as assigned.

Qualifications

• Bachelor’s degree in health science or a related field and 8+ years of clinical research experience, including meaningful responsibility for managing complex clinical trials.
• Strong global clinical trial and later-stage development experience, ideally including Phase III. Candidates with substantial experience leading large, complex Phase II studies will also be considered.
• Demonstrated ability to lead and influence cross-functional study teams.
• Hands-on experience managing CROs and vendors and proactively addressing operational risks.
• Strong working knowledge of GCP, ICH, FDA, and applicable global clinical trial requirements.
• Strong communication and problem-solving skills, with the ability to work independently, advocate for what is needed, and recognize when to engage others for support.

Preferred Capabilities

• Phase III global study experience.
• Oncology or rare disease clinical development experience.
• Experience with eTMF, EDC, IWRS, and RBQM platforms.
• Experience managing clinical study budgets and contracts.
• Experience within a fast-paced biotechnology environment.
• PMP certification or equivalent project management training.

Role Specific Additional Information

• Due to the global nature of the role, there may occasionally be a need for early-morning or evening meetings to accommodate teams and partners across time zones.
• Travel of approximately 25% may be required, including travel to Boston approximately twice per year, as well as attendance at relevant conferences or study-related meetings.

Benefits

• Competitive salary and annual bonus.
• Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
• Generous parental leave and family planning benefits.
• Outstanding culture and opportunities for personal and professional growth.