Experienced Project Manager – IVD, CRO

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🕒 April 1

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QbD Group

WebsiteLinkedInAll Job Openings

501 - 1000 employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

QbD Group is a consulting company specializing in the life sciences sector. They provide comprehensive quality assurance and regulatory affairs services, supporting companies throughout the entire product lifecycle, from traditional pharmaceuticals to advanced therapy medicinal products. With a focus on life sciences, QbD Group offers a range of services, including quality control, qualification and validation of biotech products, and clinical solutions. They emphasize safety and regulatory compliance and offer innovative digital solutions for quality management. QbD Group distinguishes itself with its commitment to fostering innovation, providing a supportive work environment, and maintaining strong industry connections.

📋 Description

• Oversee the planning and execution of all projects within the team, ensuring adherence to project governance processes • Support and guide Study Coordinators, enabling them to achieve success and deliver consistent results • Implement project management tools and templates across the team to increase operational efficiency • Continuously monitor project portfolios for risks, deviations, and resource utilization, driving actions for improvement • Lead the planning, execution, and delivery of critical strategic projects, ensuring timely and high-quality outcomes • Serve as the primary point of contact for clients and stakeholders, fostering strong relationships and effective communication • Identify risks, create mitigation plans, and ensure proactive issue resolution to keep projects on track • Develops and manages the study budget • Overall responsibility for negotiation of financial aspects of clinical performance studies/program • Interacts with senior internal management and external personnel on significant matters often requiring coordination between involved team members and stakeholders

🎯 Requirements

• Master’s, or Ph.D. in a relevant scientific discipline (e.g., Biomedical Sciences, Biotechnology, Bioscience Engineering, ...) or equivalent by experience • Minimum of 7 years’ experience in project management, with a proven track record in a CRO, IVD, medical device, or life sciences environment • Experience with managing complex, cross-functional projects with global stakeholders • Exceptional leadership, communication, and stakeholder management skills • Proven ability to develop and implement project management tools, systems, and best practices • Strong analytical and problem-solving skills with a strategic mindset • High attention to detail and organizational skills • Ability to identify and adapt to shifting priorities and competing demands • Excellent interpersonal skills; Team player • Ability to make timely and well-reasoned decisions • Ability to effectively and persuasively communicate verbally and in writing • Fluent in English; other languages are a plus • Strong experience using Microsoft applications (Excel, Word, PowerPoint, Outlook)

🏖️ Benefits

• Attractive and competitive salary package tailored to individual needs • Continuous journey of learning and development • Job security and meaningful connections • Joyful community promoting individuality