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JobsMedtronic

Project Coordinator

Medtronic

Project Coordinator

Medtronic

Macquarie Park, New South Wales, Australia

·

On-site

·

Full-time

·

2w ago

Benefits & Perks

Flexible Benefits Package

Competitive Salary

Required Skills

Data coordination

Clinical documentation management

Attention to detail

Data quality assurance

Discrepancy resolution

Audit support

Project coordination

Organization

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.

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

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About Medtronic

Medtronic

A healthcare technology company that designs and develops AI-based products and solutions for the medical industry.

10,001+

Employees

Minneapolis

Headquarters

Reviews

3.3

10 reviews

Work Life Balance

3.2

Compensation

4.0

Culture

3.4

Career

3.8

Management

3.5

65%

Recommend to a Friend

Pros

Great coworkers and supportive team

Good benefits and compensation

Growth and advancement opportunities

Cons

Aggressive leadership and cultural changes

Limited work-life balance in some roles

Company prioritizes profits over employees

Salary Ranges

1,888 data points

Mid/L4

Mid/L4 · Regulatory Affairs Specialist

151 reports

$102,623

total / year

Base

$95,683

Stock

-

Bonus

$6,940

$75,795

$140,264

Interview Experience

6 interviews

Difficulty

2.5

/ 5

Duration

14-28 weeks

Experience

Positive 0%

Neutral 67%

Negative 33%

Interview Process

1

Application Review

2

Recruiter Screen

3

Technical Phone Screen

4

Technical Interview Round 1

5

Technical Interview Round 2

6

Final Interview

Common Questions

Technical Knowledge

Coding/Algorithm

Behavioral/STAR

Past Experience