Senior Clinical Project Manager – Inflammation​/Phase 2b; Sponsor Dedicated - Remote; Preferenc

Senior Clinical Project Manager – Inflammation / Phase 2b (Sponsor Dedicated – Remote; Preference for Hybrid Foster City, CA)

Lead large‑scale global Phase 2b inflammation programs as the Global Study Lead. Responsible for end‑to‑end study execution across North America, Europe, APAC, Japan, and China.

• Lead global study execution and serve as the primary point of accountability for delivery, quality, timelines, and execution.
• Provide strategic and operational leadership throughout study start‑up, conduct, and close‑out.
• Manage interdisciplinary clinical research programs in compliance with GCP, ICH guidelines, SOPs, and applicable regulatory requirements.
• Oversee inspection readiness activities, including Trial Master File strategy and oversight.
• Coordinate activities and deliverables across CROs, vendors, and project partners.
• Lead proactive risk identification, mitigation planning, and issue resolution activities.
• Maintain oversight of project timelines, study trackers, key milestones, and critical deliverables.
• Lead cross‑functional global teams, fostering accountability, collaboration, and performance.
• Mentor project management and clinical operations staff as needed.
• Participate in bid defense meetings and support relationship development with current clients and stakeholders.
• Contribute strategic insights to support study delivery, long‑term program objectives, and process improvements.

• Minimum 5+ years of global clinical project management experience.
• Demonstrated experience serving as Global Study Lead for pivotal Phase 2b clinical trials.
• Direct experience leading complex global studies across North America, Europe, APAC, Japan, and China.
• Proven ability to lead global trials with minimal oversight, navigating operational challenges and delivering successful outcomes.
• Experience overseeing CROs, vendors, and external partners.
• Experience managing study budgets, timelines, risks, and operational deliverables at a global level.
• Strong pharmaceutical, biotechnology, CRO, or clinical research industry experience.
• Deep understanding of GCP, ICH guidelines, global regulatory requirements, drug development processes, and clinical trial operations.
• Excellent communication, presentation, stakeholder management, and interpersonal skills.
• Ability to influence without authority and drive accountability across cross‑functional teams.
• Strong organizational, planning, and project leadership skills.
• Comfortable operating independently while maintaining collaboration across stakeholders.
• Proficiency with clinical trial systems, project management tools, and emerging technologies.

$ – $

• Company car or car allowance.
• Health benefits:
  
  Medical, Dental, and Vision.
• Company match 401(k).
• Eligibility to participate in Employee Stock Purchase Plan.
• Eligibility to earn commissions/bonuses based on company and individual performance.
• Flexible paid time off (PTO) and sick time, compliant with applicable regulations.

The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.