Associate Director, Project Management, Europe

Job not on LinkedIn

🔥 15 minutes ago

🇩🇪 Germany – Remote

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Innovaderm Research Inc.

WebsiteLinkedInAll Job Openings

201 - 500 employees

💊 Pharmaceuticals

🏥 Healthcare

💼 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.

📋 Description

• 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 the Project Delivery Project Management team • Ensure appropriate resourcing and drive operational excellence across awarded studies • Act as a key integrator between project delivery and cross-functional departments • Oversee employee training, professional development, onboarding, competency development, and leadership capabilities • Partner with senior leadership to translate business objectives into effective delivery models • Provide leadership and direction for the Project Delivery function and support long-term operational planning • Own hiring of Project Managers and provide direct line management, coaching, and performance oversight • Support career development, performance reviews, succession planning, and employee relations • Oversee preparation, monitoring, and reporting of departmental KPIs • Identify workflow, process improvement, efficiency, and standardization opportunities • Ensure adoption and effective use of clinical trial systems, technology tools, company systems, and workflows • Ensure high-quality execution of project management activities and that projects meet sponsor expectations and quality standards • Review project scope, timelines, budgets, complexity, resource allocation, and forecasting • Partner with Project Directors on resource deployment, performance, workload, capability, training, and succession risks • Ensure projects are delivered on time, within budget, and according to contractual commitments • Support business continuity and client satisfaction • Advise on proactive risk and issue management and mitigation strategies • 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

🎯 Requirements

• 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

🏖️ Benefits

• Permanent full-time position • Flexible schedule • Vacation • Home-based position • Ongoing learning and development • Attractive advancement opportunities