
201 - 500 employees
đ Pharmaceuticals
đĽ Healthcare
đź Consulting
Pharmaceuticals ⢠Healthcare ⢠Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
đĽ 2 hours ago
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201 - 500 employees
đ Pharmaceuticals
đĽ Healthcare
đź Consulting
Pharmaceuticals ⢠Healthcare ⢠Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
⢠Provide senior leadership and line management oversight for the Project Management function ⢠Ensure consistent, high-quality project delivery across the portfolio in alignment with company strategy, policies, SOPs, and global regulatory requirements ⢠Build, develop, and lead a high-performing Project Delivery Project Management team ⢠Ensure appropriate resourcing and drive operational excellence across awarded studies ⢠Integrate project delivery with cross-functional departments to enable collaboration, scalability, and sponsor satisfaction ⢠Oversee employee training, professional development, compliance, and leadership capability development ⢠Partner 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 reviews, succession planning, and employee relations ⢠Ensure staffing models support business needs, delivery excellence, and sustainable workload balance ⢠Oversee preparation, monitoring, and reporting of departmental KPIs ⢠Identify workflow streamlining, process improvement, efficiency, and standardization opportunities ⢠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 delivered 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 an asset ⢠Minimum of 7 years of combined experience in clinical research and project management within a biotechnology, pharmaceutical, or CRO industry ⢠Demonstrated leadership and line management experience, preferably within a CRO environment ⢠Strong leadership, judgement, 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, Power Point) ⢠Willingness to travel up to 10% of the time ⢠Good knowledge of good clinical practices and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines ⢠Must be legally able 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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đ° Post-IPO Debt on 2019-06
â° Full Time
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