RESUME AND JOB
Medtronic
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
Responsibilities may include the following and other duties may be assigned.
Ensure that all the Clinical Study reports are run, filtered & prepared as per Clinical Safety Management and Potential Complaint Plans (CSMPCP)
Support with gathering and compiling information for reports required for potential complaint and regulatory reporting purposes
Support reconciliation activities and run listings for data cleaning in line with study milestones
Ensure that all required records are filed in the Trial Master File
Manage per Good Documentation Practice (GDP) all relevant Clinical Study files and oversee the workflow and distribution of clinical study documents
Support Clinical Event Committee (CEC) preparation and post CEC meeting activities, when applicable
Assists with periodic audits by ensuring that the applicable clinical study files are proved for completeness and accuracy
Required Knowledge and Experience:
Applicants must have completed secondary education
Practical experience with administrative tasks, operational systems, and processes
Strong attention to detail and accuracy
Clear and collaborative communication skills
Task management; prioritizing
Good knowledge of the English language written and spoken
University education/degree is welcome, but not necessary for this position.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Slovakia: 15,760.00 EUR - 23,640.00 EUR |
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here
15,760 - 23,640 EUR / yearly
Get personalized recommendations to optimize your resume specifically for Associate Clinical Safety Coordinator.. Takes only 15 seconds!
Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.


Answer 10 quick questions to check your fit for Associate Clinical Safety Coordinator. @ Medtronic.
No related jobs found at the moment.
© 2026 Pro Partners. All rights reserved.

Medtronic
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
Responsibilities may include the following and other duties may be assigned.
Ensure that all the Clinical Study reports are run, filtered & prepared as per Clinical Safety Management and Potential Complaint Plans (CSMPCP)
Support with gathering and compiling information for reports required for potential complaint and regulatory reporting purposes
Support reconciliation activities and run listings for data cleaning in line with study milestones
Ensure that all required records are filed in the Trial Master File
Manage per Good Documentation Practice (GDP) all relevant Clinical Study files and oversee the workflow and distribution of clinical study documents
Support Clinical Event Committee (CEC) preparation and post CEC meeting activities, when applicable
Assists with periodic audits by ensuring that the applicable clinical study files are proved for completeness and accuracy
Required Knowledge and Experience:
Applicants must have completed secondary education
Practical experience with administrative tasks, operational systems, and processes
Strong attention to detail and accuracy
Clear and collaborative communication skills
Task management; prioritizing
Good knowledge of the English language written and spoken
University education/degree is welcome, but not necessary for this position.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Slovakia: 15,760.00 EUR - 23,640.00 EUR |
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here
15,760 - 23,640 EUR / yearly
Get personalized recommendations to optimize your resume specifically for Associate Clinical Safety Coordinator.. Takes only 15 seconds!
Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.


Answer 10 quick questions to check your fit for Associate Clinical Safety Coordinator. @ Medtronic.
No related jobs found at the moment.
© 2026 Pro Partners. All rights reserved.