Clinical data specialist
PowerToFly, Indiana, PA, United States
As an individual contributor, the Clinical Data Specialist will be involved in clinical research projects to deliver desired outcomes while adhering to relevant policies, guidelines, and acquired skills.
Job responsibilities
Deliver assigned projects while working with multiple stakeholders to achieve desired outcomes
Learn about Stryker’s existing portfolios in the JR and MET business units including but not limited to Mako SmartRobotics, Triathlon Total Knee System, and Trident Hip system
Collaborate effectively with researchers, design engineers, software developers, surgeons, and others
Define protocol for data collection and maintenance from medical devices relevant to the project
Maintain and execute Matlab/Python scripts for data analysis and complaints
Interpret the data and logs collected from Medical device systems alongside other stakeholders
Generate insights from data collected using relevant methods and circulate for review and input by other stakeholders
Draft project reports, gather feedback on the report, and deliver them in a timely manner
Participate in cadaveric and live surgical examinations as an observer
Stay updated with latest regulations for medical devices
Adhere to ethical principles and organizational guidelines for research involving human subjects
Contribute to identifying new technological features as well as potential risks and create concepts to mitigate the identified risks
#J-18808-Ljbffr
Job responsibilities
Deliver assigned projects while working with multiple stakeholders to achieve desired outcomes
Learn about Stryker’s existing portfolios in the JR and MET business units including but not limited to Mako SmartRobotics, Triathlon Total Knee System, and Trident Hip system
Collaborate effectively with researchers, design engineers, software developers, surgeons, and others
Define protocol for data collection and maintenance from medical devices relevant to the project
Maintain and execute Matlab/Python scripts for data analysis and complaints
Interpret the data and logs collected from Medical device systems alongside other stakeholders
Generate insights from data collected using relevant methods and circulate for review and input by other stakeholders
Draft project reports, gather feedback on the report, and deliver them in a timely manner
Participate in cadaveric and live surgical examinations as an observer
Stay updated with latest regulations for medical devices
Adhere to ethical principles and organizational guidelines for research involving human subjects
Contribute to identifying new technological features as well as potential risks and create concepts to mitigate the identified risks
#J-18808-Ljbffr