We anticipate the application window for this opening will close on - 20 Jun 2025

 

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

At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.

Responsibilities may include the following and other duties may be assigned.

• Assist with designs, plans, and development of clinical evaluation research studies.
• Assist with preparing and authoring protocols, patient record forms, and other documents.
• Perform study start-up and conduct activities, including ICF review that meets regulatory requirements, creating study-specific essential document lists, managing and communicating the status of study progress and activities.
• Identify and investigate discrepancies in study documentation by applying clinical protocol and good clinical practice (GCP) knowledge and develop processes to mitigate reoccurrence throughout study phases.
• Conduct in-house and site (if applicable) reviews of associated documentation and participate in internal and competent authority audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, internal standard operating procedures (SOPs), and US and OUS regulations.
• Communicate and coordinate study activities between the study sponsor, site research coordinators, study investigators, working closely with the Clinical Research Manager, Clinical Trial Manager, and/or Project Coordinators.
• Oversees and interprets results of clinical investigations in preparation for device or consumer application.
• Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with SOP, GCP, and specific country regulations, and may prepare clinical trial budgets.
• May be responsible for clinical supply operations, site, and vendor selection.
• Represents Medtronic from a clinical research perspective within the country/region and also collects feedback from local customers and authorities.
• Builds and maintains optimal relationships and effective collaborations with various internal and external parties.
• Drives local evidence dissemination & awareness.

Qualifications

Must-Have: Minimum Requirements

• Requires a Baccalaureate degree

Nice to Have:

• Strong written, oral, and interpersonal communication skills including proficient knowledge of medical terminology.
• Computer skills (MS Office products, word processing, spreadsheets, etc.).
• High attention to detail and accuracy.
• Ability to manage multiple tasks.
• Good prioritization and organizational skills.
• Excellent problem-solving skills.

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. 

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

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.
 

Salary ranges for U.S (excl. PR) locations (USD):$65,600.00 - $98,400.00

This position is eligible for a short-term inc