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选择求职条件Medtronic神经调控与盆腔健康团队高级医学科学作家，主导科学论文撰写、文献综述及证据差距分析。与医学事务、临床研究、市场及法规团队跨部门协作，推动临床证据传播与发布策略。
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
Across our global Neuroscience organization, we advance care for some of medicine’s most complex neurological and spinal conditions. By combining innovative technology, data-driven insights, and deep clinical expertise, we partner with physicians and health systems to improve how patients are treated and supported throughout their care journey.
Join Medtronic's Neuromodulation and Pelvic Health team as a Senior Medical Science Writer and play a critical role in advancing the scientific evidence that supports our therapies. As a key member of the Pelvic Health Evidence Team, you will lead medical and scientific communication initiatives, including literature reviews, evidence gap analyses, publication planning, manuscript development, and scientific dissemination activities. You will collaborate closely with cross-functional partners across Medical Affairs, Clinical Research, Marketing, Health Economics & Reimbursement, and Regulatory teams to shape evidence strategies and communicate meaningful clinical insights to both internal and external stakeholders.
Check us out on LinkedIn: Medtronic Brain Modulation and Pain Interventions
Check us out on LinkedIn: Medtronic Pelvic Health
This highly visible role offers the opportunity to influence evidence generation, support scientific publications and presentations, engage with leading healthcare professionals, and contribute to the advancement of patient-centered care.
Responsibilities may include the following and other duties may be assigned.
Lead the development, authorship, and submission of scientific manuscripts, abstracts, posters, podium presentations, and other evidence-based medical communications derived from clinical studies, scientific research, and real-world evidence.
Conduct comprehensive literature reviews, synthesize scientific findings, develop medical evidence reports, and lead cross-functional evidence gap assessments to inform future research and evidence generation strategies.
Collaborate with physicians, healthcare professionals, and internal stakeholders to support publication planning, scientific communications, and dissemination of clinical evidence.
Facilitate publication committees and partner with physician investigators to develop and execute publication plans that address key evidence needs and support high-impact scientific publications.
Serve as a clinical and scientific evidence expert, providing support for Clinical Evaluation Reports (CERs), physician-sponsored studies, marketing material reviews, and new product evidence development.
Partner cross-functionally with Medical Affairs, Marketing, Research & Development, Health Economics & Reimbursement, Clinical Research, and Regulatory Affairs to align evidence strategies and support business objectives.
Support investigator meetings, advisory boards, research collaborations, and external partnerships, while effectively engaging senior internal and external stakeholders.
Evaluate external research proposals for scientific rigor and oversee evidence-related project deliverables, ensuring timely execution and compliance with established milestones.
Maintain databases of peer-reviewed literature, publications, and scientific evidence, and prepare responses to scientific, regulatory, audit, and submission-related inquiries.
Monitor published literature for reportable complaints or adverse events and ensure appropriate reporting in accordance with Global Clinical Health (GCH) requirements.
Ensure compliance with FDA, ISO, Medtronic quality standards, policies, and procedures while delivering high-quality scientific work.
Location: Rice Creek/Fridley (Onsite)
Onsite:
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. We’re working onsite 4 days a week to drive performance, foster an environment of belonging, and collaborate to inspire as we engineer the extraordinary. This role will require 10% of travel to enhance collaboration and ensure successful completion of projects.
Minimum requirements:
To be considered for this role, the minimum requirements must be evident on your resume.
Bachelor's degree with minimum of 4 years of clinical research experience in studies, publications, and/or program management.
OR an advanced degree (PhD preferred) with minimum of 2 years of experience in clinical research, studies, publications, or program management.
Nice to Have (Preferred Qualifications):
Experience in technical writing including clinical study plans, clinical reports, scientific manuscripts, clinical evidence reports.
Proven record in leading study publications including authorship.
Demonstrated ability in working within a matrix of cross functional stakeholders including project management skills and experience with related tools
Familiarity with ICMJE guidelines and Good Publication Practices Knowledge in the areas of neurology and/or psychiatry
Understanding of clinical research study design, Good Clinical Practices, and global clinical regulations (e.g., FDA, ICH guidelines) for medical devices, biologics, and/or pharmaceuticals.
Demonstrated ability to identify and adapt to shifting priorities and competing demands, and maintain composure in difficult circumstances
Ability to provide performance feedback and to appropriately respond to feedback from customers and coworkers
Willingness to accept challenging assignments and engage in professional developmental activities
Strong analytical and critical thinking skills with the ability to identify and resolve issues efficiently.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
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.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
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.
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
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