Principal Medical Communications Specialist - CRM na Medtronic
Medtronic · Mounds View, Estados Unidos Da América · Onsite
- Senior
- Escritório em Mounds View
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.This position will be based in Mounds View, MN.
Within the clinical science and evidence team, part of the CRM Clinical Research and Medical Affairs organization, one of our responsibilities includes management of the scientific publication process and global evidence dissemination from Medtronic-sponsored clinical trials, registries, and other research data. In this role, the Principal Medical Communications Specialist will work closely with Principal Investigators and internal team members from the clinical study team, statistics, clinical leadership and cross-functional SMEs.
With the growing volume of data, rapid advances in AI, and continuous innovation in technology, we are at a pivotal moment to reimagine how scientific evidence is disseminated. As access to information becomes commoditized – easy, fast, and inexpensive – our ability to understand and impact humanity becomes more critical than ever.
This newly created role will collaborate across internal and external partners to define and execute scientific dissemination strategies. The primary focus will be to identify channels, formats, and content that tailor scientific and medical results and data by audience segment, based on expertise, literacy, and needs. The medical communication professional will use a range of techniques to assess understanding and increase engagement.
Responsibilities:
- Translate complex scientific and medical information into clear, accessible language for diverse audiences, including clinicians, healthcare providers, patients, caregivers, and regulators.
- Develop and implement data-driven scientific evidence communication strategies that align with dissemination goals, audience needs and preferred formats and channels – maximizing our evidence footprint through ‘Evidence for Action’.
- Conduct audience analysis to define the needs, interests, and knowledge level of the target recipients.
- Create high-quality medical and scientific content, including manuscripts, abstracts, presentations, plain language summaries, graphical abstracts, white papers, and other innovative formats.
- Tailor writing style, tone, and level of detail to ensure content is appropriate and engaging for each audience.
- Manage the project timeline for each deliverable through final delivery (e.g. peer-review publication, scientific conference presentation) ensuring compliance to regulatory, medical society, and corporate standards.
- Interface with physicians, clinical leadership, and other stakeholders to align evidence dissemination activities and deliverables
- Maintain an in-depth knowledge of key therapy and product areas, stay abreast of current literature relevant to CRM therapies and products (including competitors)
- Collaborate with subject matter experts, such as researchers, clinicians, and regulatory affairs, to gather information and ensure accuracy.
Must Have: Minimum Requirements
To be considered for this role, please ensure the minimum requirements are evident in your applicant profile.
- Bachelor’s degree required
- Minimum of 7 years of clinical/medical/scientific writing experience
- Or advanced degree with a minimum of 5 years clinical/ medical/ scientific writing experience
Nice to Have
- Advanced degree in life sciences, medicine, or a related field (e.g., MS, MD, PharmD, PhD).
- Demonstrated ability to write for various audiences with different levels of scientific understanding.
- Demonstrated knowledge of physiology and/or applicable disease states, medical terminology, CRM therapies and technologies
- Experience authoring peer-reviewed manuscript and abstract presentations at major scientific conferences
- Proven track record of developing clear and concise documents.
- Excellent organizational and project management skills.
- Proven track record of excellent writing skills (medical writing certification is a plus: CMPP, BELS, AMWA, MWC)
- Excellent interpersonal, presentation, and communication 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.
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
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 95,000+ 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.
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.
