
Associate Director, Project Management
Posted Oct 16

Posted Oct 16
This is a fully remote position, open to applicants in Ireland.
• Provide senior leadership and oversight for the Project Management function.
• Ensure the delivery of high-quality projects that align with company strategy, policies, SOPs, and global regulatory requirements.
• Build, develop, and lead the Project Delivery Project Management team.
• Ensure adequate resourcing and promote operational excellence across assigned studies.
• Integrate project delivery with cross-functional departments to facilitate collaboration, scalability, and sponsor satisfaction.
• Oversee the onboarding, training, professional development, competency development, and retention support of employees.
• Act as a strategic partner to senior leadership, translating business objectives into effective delivery models.
• Provide leadership and direction for the Project Delivery function and assist in workforce planning.
• Contribute to continuous improvement initiatives within project delivery, systems, and workflows.
• Lead, coach, and supervise the performance of Project Managers, including PM I, PM II, and Senior PMs.
• Manage the hiring process for new Project Managers.
• Support career development through feedback, goal setting, performance reviews, and succession planning.
• Foster a collaborative, high-accountability team culture.
• Serve as the primary point of contact for employee relations matters.
• Oversee the preparation, monitoring, and reporting of departmental KPIs.
• Identify opportunities for workflow streamlining, process improvement, efficiency, and standardization.
• Ensure the effective adoption of clinical trial systems, technology tools, company systems, and workflows.
• Guarantee high-quality execution of Project Management activities and sponsor-aligned project delivery.
• Review project scope, timelines, budgets, and complexity to inform resource allocation and forecasting.
• Collaborate with Project Directors on resource deployment, workload, performance, capability, and project delivery needs.
• Identify resource gaps, training needs, and succession risks, implementing mitigation plans as necessary.
• Ensure projects are completed on time, within budget, and according to contractual obligations.
• Maintain business continuity and client satisfaction.
• Provide advice on proactive risk and issue management and mitigation strategies.
• Mentor Project Managers in proactive planning, stakeholder management, and problem resolution.
• Share lessons learned and best practices with internal stakeholders.
• Partner with senior leadership to ensure consistency, scalability, and alignment of delivery practices.
• Contribute to the long-term vision and continuous improvement of the Project Delivery department.
• Ensure compliance with SOPs, Good Clinical Practices (GCP), ICH guidelines, and global regulatory requirements.
• Write, review, and maintain SOPs, tools, and process documentation.
• Support audit and inspection readiness.
• Perform additional responsibilities as needed when qualified and appropriately trained.
• About Indero: provide comprehensive dermatology and rheumatology clinical research and trial delivery for biotech and pharmaceutical sponsors.
• 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.
• Proven 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 while managing multiple priorities.
• Capability to build strong relationships with internal teams, sponsors, and external partners.
• Excellent proficiency in Microsoft Office (Word, Excel, PowerPoint).
• Willingness to travel up to 10% of the time.
• Strong knowledge of good clinical practices and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines.
• Applicants must have the legal right to work in the EU.
• Permanent full-time position.
• Flexible schedule.
• Vacation.
• Home-based position.
• Ongoing learning and development.
• Attractive advancement opportunities.
• Up to 10% travel allowance/requirement.
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