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You will be updated with latest job alerts via emailAt Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll 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:
Provides project and administrative support for Clinical VMO team and back up support as needed
Schedules coordinates manages and monitors meetings for Clinical VMO taking notes on discussion points and action items to ensure proper follow-through
Responds and follow up to stakeholder requests interfacing directly with various levels of internal customers
Supports OU study teams in the organization and maintenance of clinical study documentation as needed.
Maintains reports and dashboards with supplier data.
Supports the team in publishing quarterly Medtronic Clinical Approved Supplier List (MCASL)
When back up support needed understanding in the Suppliers and Services on the MCASL and support discussions with clinical teams regarding supplier needs with manager oversight.
Maintains business processes to ensure audit readiness in: MCASL Performance Evals Risk assessments and other regulated areas as
Collects maintains reviews group highlights and KPIs on a monthly quarterly and yearly timeframe
Monitors and Maintains VMO training documents and compliance trackers Teams sites and SharePoint
Supports daily projects where use of Excel Power Point SCTMS Veeva Vault and RAD is
Supports team in creating Medtronic brand presentations and documentation
Required Knowledge and Experience:
To be considered for this role the minimum requirements must be evident on your resume
High School Degree
High level of English verbal and written comprehension
Minimum of 4 years of office support and coordination experience
Proficiency in Microsoft Office is a must
Nice to Have (Preferred Qualifications):
Experience working with or for Contract Research Organization (CROs)
Experience working with suppliers supporting clinical study operations
Experience with Clinical Trial Management System and Trial Management Files
Experience reviewing filing and managing Quality Records
Experience in working in a regulated environment/industry
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.
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 95000 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
Required Experience:
IC
Full-Time