Medtronic
Principal Field Clinical Engineer(m/w/x)
Full-timeWith HomeofficeSenior
Meerbusch
from 88,800 / year
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SHSHQ Medtronic Int. Trading Sàrl
Senior Clinical Research Monitor(m/w/x)
Meerbusch
from 105,960 / year
Full-timeWith Home OfficeSenior
Nejo AI Summary
Coordinating and executing clinical trial monitoring with risk-based data verification for healthcare technology solutions. Clinical monitoring or study management experience required. Medtronic Incentive Plan.
Requirements
- Degree in life sciences, healthcare, or equivalent
- Experience in clinical monitoring, operations, or study management
- Strong project coordination and attention to detail
- Problem solving mindset and pro-active attitude
- Ability to work with minimal supervision
- Strict adherence to procedures, SOPs, and regulations
- Flexibility and strong adaptability to change
- Willingness to travel approximately 25%
- Customer focused team player
- Mature personality and inclusive collaboration skills
- Ability to cultivate relationships
- Curiosity and creative thinking
- Fluent English communication skills
- Ability to manage multiple tasks
- Strong quality focus
Tasks
- Coordinate and execute all clinical trial monitoring activities
- Follow SOPs, GCP guidelines, and country-specific regulations
- Develop and maintain monitoring study documentation
- Implement risk-based monitoring and targeted source data verification
- Plan and coordinate monitoring visit schedules
- Review monitoring visit reports and action items
- Escalate monitoring issues and coordinate their resolution
- Perform quality checks to ensure audit and inspection readiness
- Manage centralized monitoring and clinical device accountability
- Support study start-up activities with the study manager
- Prepare investigator meetings and site initiation visits
- Train the monitoring team and hospital staff
- Collaborate with internal and external stakeholders
- Oversee vendor and CRO monitoring activities
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Bonuses & Incentives
- Medtronic Incentive Plan
Competitive Pay
- Competitive compensation plans
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SHQ Medtronic Int. Trading Sàrl and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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SHSHQ Medtronic Int. Trading Sàrl
Senior Clinical Research Monitor(m/w/x)
Meerbusch
from 105,960 / year
Full-timeWith Home OfficeSenior
Nejo AI Summary
Coordinating and executing clinical trial monitoring with risk-based data verification for healthcare technology solutions. Clinical monitoring or study management experience required. Medtronic Incentive Plan.
Requirements
- Degree in life sciences, healthcare, or equivalent
- Experience in clinical monitoring, operations, or study management
- Strong project coordination and attention to detail
- Problem solving mindset and pro-active attitude
- Ability to work with minimal supervision
- Strict adherence to procedures, SOPs, and regulations
- Flexibility and strong adaptability to change
- Willingness to travel approximately 25%
- Customer focused team player
- Mature personality and inclusive collaboration skills
- Ability to cultivate relationships
- Curiosity and creative thinking
- Fluent English communication skills
- Ability to manage multiple tasks
- Strong quality focus
Tasks
- Coordinate and execute all clinical trial monitoring activities
- Follow SOPs, GCP guidelines, and country-specific regulations
- Develop and maintain monitoring study documentation
- Implement risk-based monitoring and targeted source data verification
- Plan and coordinate monitoring visit schedules
- Review monitoring visit reports and action items
- Escalate monitoring issues and coordinate their resolution
- Perform quality checks to ensure audit and inspection readiness
- Manage centralized monitoring and clinical device accountability
- Support study start-up activities with the study manager
- Prepare investigator meetings and site initiation visits
- Train the monitoring team and hospital staff
- Collaborate with internal and external stakeholders
- Oversee vendor and CRO monitoring activities
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Bonuses & Incentives
- Medtronic Incentive Plan
Competitive Pay
- Competitive compensation plans
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SHQ Medtronic Int. Trading Sàrl and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
SHQ Medtronic Int. Trading Sàrl
Industry
Healthcare
Description
The company leads global healthcare technology and seeks solutions to challenging health problems.
Not a perfect match?
- Medtronic
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