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Medtronic

Project Coordinator

Reposted Yesterday
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Remote
Hiring Remotely in The Park, New South Wales
Mid level
Remote
Hiring Remotely in The Park, New South Wales
Mid level
The Clinical Studies Support Coordinator supports clinical studies by coordinating data, managing clinical documents, ensuring data quality, and resolving any discrepancies.
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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 LifeWe’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.
Together, we can confront the challenges that will change the face of healthcare. Join us for a career that changes quality of lives for patients.

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- actively participates in the development and testing of case report forms, study reports, and study databases based on protocol requirements.

  • Ensures timely and quality completion of data forms, verifies study data, and generates, manages and resolves data discrepancies.

  • 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: 

  • Requires minimum of 4 years of relevant experience in supporting clinical studies, with hands-on involvement in data coordination and clinical documentation management.

  • Strong attention to detail with experience ensuring data quality, resolving discrepancies, and supporting audits for accuracy and compliance.

  • Organised and proactive team player, capable of managing multiple tasks, timelines, and stakeholder interactions in a clinical research environment


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  
 

Top Skills

Case Report Forms
Clinical Documentation Management
Data Coordination
Study Databases
Study Reports

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