Clinical Study Manager

Bedrijfsomschrijving

You are a part of Building up the clinical expertise within Philips. You will serve the Grooming & Beauty Business in Philips. You will work closely together with several teams including Regulatory, Marketing, and Product Development.

In this role, you have the opportunity to Impact through the development and testing of quality Philips products and solutions that help countless people worldwide

You are responsible for

• Leads the management of clinical studies, in compliance to all applicable regulations (like ISO, GCP and FDA) and Philips procedures.
• Ensures strict adherence to study protocols, regulatory standards, and Philips Processes/Procedures through meticulous execution of site assessment, on site and remote monitoring and training, and close-out visits, proactively addressing deviations and ensuring data accuracy and study integrity.
• Collaborates with study sites and investigators to provide support and guidance on protocol requirements, study procedures, and regulatory expectations.
• Acts as a subject matter expert to provide guidance on GCP, ISO and FDA regulatory requirements for the conduct of research involving human subjects is required in the medical device industry.
• Reviews project documentation and deliverables for accuracy, completeness, and compliance with established protocols and regulatory requirements, and GCP guidelines.
• Enhances study procedures and processes to optimize efficiency and data quality throughout the clinical research lifecycle and performs data review and verification activities to ensure accuracy and consistency of clinical trial data.
• Ensures resolution of queries, issues, and discrepancies related to study conduct, data collection, and regulatory compliance in a timely and effective manner.
• Leads relationship and management activities relationships within the Clinical and Medical functions, as well as cross-functionally with Regulatory, R&D, Quality, HEMAR, Biostatistics and Data Management, Clinical Development, and other internal partners to achieve project objectives.
• Develops study plans and protocols, integrating regulatory requirements, Good Clinical Practice (GCP) guidelines, and study objectives to ensure robust study design and execution.
• Utilizes clinical trial applications including Electronic Data Capture (EDC), Electronic Trial Master File (eTMF), and Clinical Trial Management System (CTMS) with high level of competency.
• Fosters effective collaboration and communication with across cross-functional teams and external collaborators, facilitating problem-solving, decision-making, and alignment on study objectives and priorities throughout the project lifecycle.
• Monitors study progress, conducting in-depth analysis of trends and deviations to inform proactive decision-making, risk mitigation strategies, and continuous improvement initiatives, ensuring budgets and schedules meet corporate requirements.

• Salary: Best in the market.
• Holiday Allowance – 8% of your annual salary, ensuring you can fully enjoy your time off.
• Pension Plus Scheme – Secure your future with our comprehensive retirement plan.
• Home Office Setup – Receive a €750 net allowance to create a comfortable and productive workspace.
• Time to Recharge – Enjoy 25 vacation days per year (based on a 40-hour workweek).
• Travel Allowance – Support for commuting expenses.
• Internet Allowance – Contribute to seamless remote work.
• Relocation Assistance – Moving to the Netherlands? We’ve got you covered.