The Clinical Research Associate is responsible for supporting various aspects of clinical research activities, ensuring adherence to regulatory requirements and Good Clinical Practice (GCP) guidelines, working under some supervision. The role enhances study procedures and processes to optimize efficiency and data quality throughout the clinical research lifecycle. The role executes site initiation, monitoring, and close-out visits, identifies potential risks, and implements corrective actions to address deviations and non-compliance. The role interacts with study stakeholders, tracks study progress against milestones and budgetary constraints, and provides support and guidance to study sites and investigators on protocol requirements.
Your role:
In collaboration with internal stakeholders, support the initiation and execution of clinical investigations (feasibility, pivotal, and real-world evidence) to validate the value proposition for the target market
Create study training materials for hospital site research staff
Participate in on-site training activities to support site initiation and continuous education as needed.
Support anesthesiologists/intensivists/study staff in the conduct of intraoperative and intensive care unit hemodynamic clinical studies using arterial lines and pulmonary artery thermodilution catheters
Support and/or monitor study staff in capturing hemodynamic measurements
Represent internally the voice of clinical end-users and gaining a deep understanding of clinical workflow, delivery of care, and unmet operational requirements
Performing study monitoring visits per ISO14155/Good Clinical Practice
Be able to handle multiple sites and projects at any given time
You're the right fit if:
Bachelor's Degree in Nursing or equivalent (e.g. apprenticeship as nurse)
4+ years of in‐depth knowledge of the critical care environment (OR and/or ICU)
Deep knowledge of invasive hemodynamic monitoring techniques
Exceptional communication and presentation skills
High comfort level with technology and nursing informatics concepts
English and German language capabilities and willingness to re‐locate to Munich, Germany
Willingness to travel overnight up to 50% of the time, including internationally
How we work together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.
Onsite roles require full-time presence in the company’s facilities.
Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.
Indicate if this role is an office/field/onsite role.
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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• Discover our rich and exciting history.
• Learn more about our purpose.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.
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