Key Facts

Remote From:

Full time

English

Hard Skills

Clinical Trial Planning MATLAB Python (Programming Language) Medical Device Directive Medical Device Directive Ethical Research Analytics Surgical Pathology Stakeholder Communications Project Coordination +5 more

Other Skills

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Report Writing
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Communication
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Time Management
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Teamwork
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Detail Oriented

Roles & Responsibilities

Proficiency in Matlab and Python for data analysis and scripting in a clinical research setting
Experience defining data collection protocols and maintaining data from medical devices, including interpretation of device logs
Strong collaboration skills across cross-functional teams including researchers, design engineers, software developers, and surgeons
Knowledge of medical device regulations and ethical guidelines for research involving human subjects

Requirements:

Deliver assigned projects while collaborating with multiple stakeholders to achieve desired outcomes
Define protocols for data collection and maintenance from medical devices relevant to the project
Maintain and execute Matlab/Python scripts for data analysis and management of complaints
Draft project reports, gather feedback, and deliver them in a timely manner

Stryker

About Stryker

Stryker is a global leader in medical technologies and, together with our customers, we are driven to make healthcare better. We offer innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. More information is available at stryker.com and careers.stryker.com. Facts: ● 2023 Sales: $20.5 billion ● Industry: Medical Instruments & Supplies ● Employees: 52,000 worldwide ● 40 years of sales growth leading up to 2020 ● 44+ Manufacturing and R&D Locations Worldwide ● $1.4 billion spent on research and development in 2023 ● ~12,900 patents owned globally in 2023 ● Products sold in ~75 countries ● Fortune 500 Company ● 7 consecutive years as one of Fortune's World's Best Workplaces Stryker’s social media community guidelines: https://www.stryker.com/content/m/legal/social-media-community-guidelines/en/index.html Notice Regarding Employee Conduct on Facebook/LinkedIn Meta/LinkedIn does not permit employers to verify or validate “employees” in the (META: “Works at” LinkedIn: “Experience”) section of users’ profiles. Please be aware that the views expressed by individuals on their personal accounts and do not necessarily represent the views of our company. If you encounter any issues with a person claiming to be our employee, we recommend using the “Report Profile” feature. If you’d like to report concerns to our Ethics Hotline, you may do so at: https://app.convercent.com/en-us/LandingPage/b6bb4e84-9fcb-ea11-a974-000d3ab9f296

Company type: XLarge

Founded: 2018

Company size: 10001

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Job description

Work Flexibility: Hybrid

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

Travel Percentage: None