At 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.

A Day in the Life

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

Support in the design and implementation of the Scientific project in compliance with GCP and regulatory standards.

Contributes to scientific projects with close supervision using specialized knowledge and skills.

Monitor trial progress conduct site visits and ensure adherence to SOPs and timelines.

Oversee budgets timelines for assigned projects.

Collaborate with cross-functional teams.

Translate complex clinical data into clear compelling messages for diverse audiences.

Develop presentations and communication materials for internal and external stakeholders.

Contribute to the development of training materials and educational content for clinical staff

Support in the preparation review and filing of clinical study documents including protocols investigator brochures informed consent forms and final study reports.

Draft scientific manuscripts abstracts and posters for publication and presentation.

Ensure clarity accuracy and scientific integrity in all written materials.

Support regulatory submissions with well-documented and compliant content.

Reviews summarizes and maintains databases of peer-reviewed and internally created scientific literature.

Reports complaints or adverse events identified in the literature to Global Clinical Health (GCH).

Prepares responses to audit and submission queries.

May collaborate with external healthcare professionals to develop scientific content.

Required Knowledge and Experience:

A Bachelors or Masters degree in a scientific field.

Excellent written and spoken English.

Analytical and problem-solving abilities.

Detail-oriented with organizational skills.

Excellent written and verbal communication skills.

Ability to synthesize scientific data and communicate effectively.

At least 2 years of experience in clinical research medical writing or scientific communication.

The ability to perform literature reviews.

Ability to manage multiple projects and meet deadlines independently.

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 clinical 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.

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.

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 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