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Clinical Research Associate
2 months ago
About the Position
We are seeking a highly skilled Clinical Research Associate to support the execution of Clinical Trials for our Hospital Patient Monitoring Business. As a key member of our team, you will work closely with the Clinical Operations Manager to ensure timely releases of innovative products that deliver high quality and outstanding reliability to the lives they will improve.
Your Key Responsibilities
- Own the overall study process and adherence to clinical trial procedures, identifying potential problems and risks, and implementing mitigation plans to ensure timely completion.
- Support electronic data capture (EDC) user acceptance testing and training, and liaise with project team members to resolve study site issues and data queries.
- Contribute to the creation of informed consent forms, study status reports, and accurate study files, and support the development of regulatory binders and investigational product shipments as needed.
- Travel to study sites for meetings and monitoring visits, with approximately 60% travel and 10% international.
Requirements
- 2+ years of experience in clinical trials, preferably in a healthcare setting, CRO, medical device, or medical technology industry.
- Bachelor's degree in biological sciences or healthcare.
- Ability to perform the minimum physical, cognitive, and environmental job requirements with or without accommodation.
- Autonomy, fluidity, and ability to follow through on timelines, projects, and tasks with limited direction.
About Philips
We are a health technology company committed to improving the lives of others. Our mission is to provide quality healthcare to everyone, everywhere. Join us in making a difference and doing the work of your life.
