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Medtronic
Bogota, Columbia
(on-site)
Job Type
Full-Time
Project Coordinator II
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Project Coordinator II
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Description
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.A Day in the Life
We're a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Work with us to incentivize better patient care and partner across the industry to make healthcare more affordable and accessible. Be a part of a community of experts committed to ensuring quality, affordable healthcare worldwide.
This position supports the execution and maintenance of clinical studies by managing essential operational and documentation tasks. The role involves coordinating data collection and reporting to regulatory bodies, processing compensation and resolving discrepancies, and ensuring the organization, accuracy, and completeness of clinical study files. Additionally, it requires overseeing document control processes, assisting with periodic audits, and maintaining compliance with industry standards. This position will be a Remote position in Bogotá
Responsibilities may include the following and other duties may be assigned:
- Supports clinical studies by executing and maintaining one or more of the following areas.
- Data coordination; data reporting to regulatory bodies
- May process compensation & identify and resolve compensation discrepancies.
- Document coordination - creates and manages the clinical study files and oversees the organization and distribution of clinical study documents.
- Assists with periodic audits of clinical study files for completeness and accuracy.
Required Knowledge and Experience:
- Bachelor's degree is advantageous
- One to two years of experience supporting clinical research, data coordination or document management is preferred
- Advanced communication skills (written & verbal)
- Knowledge of Microsoft Office Applications (Word, Excel, Access, PowerPoint, Outlook)
- Fluent in English
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.
Benefits & Compensation
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.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
About Medtronic
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
Job ID: 80801463
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