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.

REQUIRED KNOWLEDGE AND EXPERIENCE:

• A Bachelor’s or Master’s degree in a scientific field
• Excellent written and spoken English
• A minimum of two years of experience in medical writing
• The ability to perform literature reviews
• Strong collaboration skills to work effectively in a global, multidisciplinary team
• Flexibility and proactivity.
  Medical Writing certifications, Project Management skills, proficiency in additional languages, and a background in regulatory affairs are desirable qualities for this role, enhancing the ability to manage projects efficiently, navigate regulatory requirements, and communicate effectively in a global healthcare 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.

• Developing and/or updating regulatory and non-regulatory documents
• Writing and editing manuscripts on clinical studies and/or scientific reports, including special summaries from raw data for submission to regulatory agencies or internal use, monographs, comprehensive reviews, scientific exhibits, and other medical communication projects
• Synthesizing published medical and scientific literature, clinical study data, or other relevant sources to disseminate evidence
• Performing literature reviews (both systematic and non-systematic) and related data extraction
• Compiling, analyzing, and summarizing additional data from other sources as needed.