
Associate Director, Project Management
Posted Oct 16

Posted Oct 16
This is a fully remote position, open to applicants in Poland.
• Provide senior leadership and oversee line management for the Project Management function.
• Ensure consistent and high-quality project delivery across the portfolio in accordance with company strategy, policies, SOPs, and global regulatory requirements.
• Build, develop, and lead a high-performing Project Delivery Project Management team.
• Ensure appropriate resource allocation and drive operational excellence across awarded studies.
• Integrate project delivery with cross-functional departments to foster collaboration, scalability, and sponsor satisfaction.
• Oversee employee training, professional development, compliance, and the development of leadership capabilities.
• Collaborate with senior leadership to translate business objectives into effective delivery models.
• Provide leadership and direction for the Project Delivery function and support workforce planning.
• Lead, develop, hire, coach, and manage Project Managers, including PM I, PM II, and Senior PMs.
• Oversee onboarding, role-specific training, competency development, feedback, performance evaluations, succession planning, and employee relations.
• Ensure staffing models meet business needs, delivery excellence, and a sustainable workload balance.
• Oversee the preparation, monitoring, and reporting of departmental KPIs.
• Identify opportunities for workflow streamlining, process improvement, efficiency, and standardization.
• Ensure effective adoption of clinical trial systems, technology tools, company systems, workflows, and processes.
• Review project scope, timelines, budgets, complexity, resource allocation, and forecasting.
• Partner with Project Directors on resource deployment, performance, workload, capability, and mitigation plans.
• Ensure projects are completed on time, within budget, contractual commitments, quality standards, business continuity, and client satisfaction.
• Serve as a senior advisor for proactive risk and issue management.
• Mentor Project Managers in planning, stakeholder management, and problem resolution.
• Share lessons learned and best practices with internal stakeholders.
• Write, review, and maintain SOPs, tools, and process documentation.
• Support audit and inspection readiness.
• Perform other assigned responsibilities when qualified and adequately trained.
• B.Sc. in a field relevant to clinical project management.
• PMP certification is an asset.
• Minimum of 7 years of combined experience in clinical research and project management within the biotechnology, pharmaceutical, or CRO industry.
• Demonstrated leadership and line management experience, preferably in a CRO environment.
• Strong leadership, judgment, problem-solving, organizational, and communication skills.
• Ability to work effectively in a fast-paced, evolving environment and manage multiple priorities.
• Ability to build strong relationships with internal teams, sponsors, and external partners.
• Excellent proficiency with Microsoft Office (Word, Excel, PowerPoint).
• Willingness to travel up to 10% of the time.
• Good knowledge of good clinical practices and applicable Health Canada and FDA regulations/guidelines.
• Must be legally authorized to work in the EU.
• Permanent full-time position.
• Flexible schedule.
• Vacation.
• Home-based position.
• Ongoing learning and development.
• Attractive advancement opportunities.
• Equal opportunity and accommodations throughout the recruitment and selection process, upon request.
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