
Director, Project Management – Evidence Development Solutions
Posted 2 days ago

Posted 2 days ago
This is a fully remote position, open to applicants in United States.
• Lead and nurture a team of Clinical Project Managers overseeing clinical studies and observational research initiatives.
• Oversee the recruitment, onboarding, mentoring, performance evaluations, career growth, succession planning, and performance enhancement measures.
• Establish and uphold KPIs related to milestones, budgets, quality, client satisfaction, revenue generation, utilization, and retention.
• Execute resource allocation strategies and ensure team utilization remains within targeted ranges.
• Take ownership of contingency planning for leave coverage, attrition, portfolio increases, and concentration risks.
• Propel the adoption of SOPs, RACI, governance frameworks, QMS, and enterprise systems.
• Engage in Project Reviews to pinpoint risks, mentor PMs, uphold standards, and implement corrective actions.
• Ensure the accuracy of Planisware milestone, baseline, and financial forecast updates.
• Advocate for inspection readiness and track portfolio health.
• Collaborate with Quality Assurance on CAPA implementation, audit responses, and SOP enhancements.
• Represent UBC in governance meetings, business reviews, and escalation discussions as required.
• Provide executive-level communication and status updates for clients and leadership.
• Work in partnership with Data Management, Clinical Operations, Biostatistics, Medical Writing, Regulatory, Site Management, HR, Finance, and Segment leadership.
• Assist in organizational design, compensation planning, and capacity forecasting.
• A bachelor's degree in life science, health science, or a related discipline is required.
• A minimum of 10 years of clinical project management experience in a CRO, pharmaceutical, or biotech environment.
• At least 5 years of direct experience in people management.
• Proven track record in leading teams that deliver full-service clinical trials and/or PASS, registries, and RWE programs.
• Capability to lead teams responsible for revenue generation, margin management, and change order implementation.
• Proficiency in project management methodologies, resource planning, risk management, and contingency strategies.
• Strong expertise in Planisware, CTMS, financial forecasting tools, SharePoint, Teams, Excel, and Copilot.
• Experience with regulatory inspection readiness involving FDA, EMA, and Health Canada.
• Familiarity with GCP/ICH standards.
• Exceptional written and verbal communication skills at an executive level.
• Ability to distill complex issues into straightforward decisions and recommendations.
• Capacity to hold teams accountable for KPIs while fostering talent development and maintaining engagement.
• Comfortable working in a matrixed and global environment with teams across the US and Europe.
• An advanced degree (MS, PharmD, PhD, MBA) is preferred.
• PMP or equivalent certification is preferred.
• Opportunities for remote work.
• Competitive salary packages.
• Opportunities for career advancement and promotion.
• 401K plan with company matching.
• Tuition reimbursement available after 90 days of employment.
• Flexible work environment.
• Discretionary paid time off (PTO).
• Paid holidays.
• Employee assistance programs.
• Comprehensive medical, dental, and vision insurance.
• Health Savings Account (HSA)/Flexible Spending Account (FSA).
• Telemedicine services (virtual doctor appointments).
• Wellness programs.
• Adoption assistance programs.
• Short-term disability coverage after 90 days of employment.
• Long-term disability insurance.
• Life insurance coverage.
• Employee discount programs.
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