1

Clinical Strategy Manager Jobs in Minnesota (NOW HIRING)

Clinical Marketing Manager

Plymouth, MN · On-site

$110K - $150K/yr

Gain broader exposure across physician engagement, marketing strategy, customer education, and ... The Clinical Marketing Manager will serve as a key partner to FLEX Vascular leadership, physician ...

The Clinical Laboratory Business Development Manager is a front-line quota-carrying teammate ... Develops and executes strategic territory plans to prioritize, pursue, and convert competitive ...

Gain broader exposure across physician engagement, marketing strategy, customer education, and ... The Clinical Marketing Manager will serve as a key partner to FLEX Vascular leadership, physician ...

Experience developing clinical strategies and study design * Experience in structural heart therapies * Experience working with global teams * Project management experience For Baccalaureate degrees ...

Experience developing clinical strategies and study design * Experience in structural heart therapies * Experience working with global teams * Project management experience For Baccalaureate degrees ...

Experience developing clinical strategies and study design * Experience in structural heart therapies * Experience working with global teams * Project management experience For Baccalaureate degrees ...

MN · On-site

$45 - $47/hr

Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The ... implementation of mitigation strategies. Review of study data to detect anticipated and ...

Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The ... mitigation strategies. * Review of study data to detect anticipated and unanticipated issues ...

Showing results 41-60

Clinical Strategy Manager information

See Minnesota salary details

$39.2K

$77.7K

$120.5K

How much do clinical strategy manager jobs pay per year?

As of Sep 4, 2026, the average yearly pay for clinical strategy manager in Minnesota is $77,716.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,700.00 and $86,700.00 per year, depending on experience, location, and employer.

What is a clinical strategy manager?

A Clinical Strategy Manager is a professional responsible for developing and implementing strategies to improve clinical operations, patient outcomes, and organizational efficiency within healthcare settings. They analyze data, collaborate with medical staff, and ensure alignment with regulatory standards and organizational goals. This role often involves project management, process improvement, and overseeing the execution of clinical initiatives. Clinical Strategy Managers play a key part in driving innovation and supporting the long-term success of healthcare organizations.

How does a clinical strategy manager typically collaborate with cross-functional teams to drive clinical initiatives?

A Clinical Strategy Manager often works closely with teams such as clinical operations, regulatory affairs, medical affairs, and commercial departments to develop and implement effective clinical strategies. This collaboration involves leading strategic planning meetings, sharing insights on clinical trial designs, and ensuring alignment with organizational goals. The role requires strong communication skills to bridge the gap between scientific, operational, and business objectives, enabling the successful execution of clinical programs. Regular cross-functional interactions also provide opportunities to learn from different disciplines and contribute to broader organizational success.

What are the key skills and qualifications needed to thrive as a clinical strategy manager, and why are they important?

To thrive as a Clinical Strategy Manager, you need expertise in healthcare management, clinical operations, data analysis, and typically a background in nursing, pharmacy, medicine, or a related field with a relevant advanced degree. Familiarity with healthcare analytics tools, project management software, and regulatory compliance systems is crucial. Strong leadership, strategic thinking, and excellent communication skills help drive cross-functional teams and influence organizational initiatives. These capabilities are essential for developing effective clinical programs, ensuring regulatory compliance, and achieving improved patient and organizational outcomes.

What is the difference between Clinical Strategy Manager vs Clinical Operations Manager?

AspectClinical Strategy ManagerClinical Operations Manager
Primary FocusDeveloping long-term clinical strategies and initiativesManaging day-to-day clinical operations and project execution
Required CredentialsTypically advanced degrees in life sciences or healthcare, experience in strategic planningExperience in clinical project management, often with similar healthcare backgrounds
Work EnvironmentStrategic planning teams, senior leadershipOperational teams, clinical sites, project teams
Industry UsagePharmaceuticals, biotech, healthcare organizationsPharmaceuticals, biotech, clinical research organizations

The Clinical Strategy Manager focuses on developing and guiding long-term clinical strategies, while the Clinical Operations Manager handles the daily management of clinical trials and operations. Both roles are essential in the clinical development process but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Strategy jobs in Minnesota?

The most popular types of Clinical Strategy jobs in Minnesota are:

What are popular job titles related to Clinical Strategy Manager jobs in Minnesota?

For Clinical Strategy Manager jobs in Minnesota, the most frequently searched job titles are:

What cities in Minnesota are hiring for Clinical Strategy Manager jobs?

Cities in Minnesota with the most Clinical Strategy Manager job openings:

Infographic showing various Clinical Strategy Manager job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 10% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $77,716 per year, or $37.4 per hour.

Principal Clinical Evaluation Medical Writer - NMPH - Fridley, MN (Onsite)

Medtronic

Fridley, MN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago


Medtronic rating

7.9

Company rating: 7.9 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

154th of 545 rated manufacturers


Job description

We anticipate the application window for this opening will close on - 31 Aug 2026


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.

A Day in the LifeAcross our global Neuroscience organization, we develop innovative therapies for complex neurological, spinal, and pelvic health conditions. Our Neuromodulation team delivers advanced solutions for chronic pain and movement disorders through spinal cord stimulation, deep brain stimulation, and targeted drug delivery systems. Our Pelvic Health team advances minimally invasive neuromodulation therapies for bladder and bowel control conditions, helping patients regain function and improve quality of life.
Located at Medtronic's location in Rice Creek/Fridley, MN, this role is onsite four days per week and requires <10% travel.

Check us out on LinkedIn:Medtronic Brain ModulationandPain Interventions

Check us out on LinkedIn:Medtronic Pelvic Health

A Day in the Life

As a Principal Clinical Evaluation Medical Writer, you will translate complex clinical and scientific evidence into clear, defensible clinical evaluation deliverables that support regulatory compliance, submissions, and business decisions across Neuromodulation and Pelvic Health therapies. Partnering with cross-functional teams, you will assess evidence from literature, clinical studies, real-world data, post-market surveillance, risk management, and testing activities to evaluate device safety, performance, and clinical benefit. You may also contribute to broader regulatory and medical writing initiatives, including evidence summaries, benefit-risk assessments, regulatory responses, and clinical strategy activities that support regulatory success and improved patient outcomes.

This role offers the opportunity to shape how clinical evidence is evaluated and communicated for therapies that improve patients' lives. In addition to developing deep expertise in clinical evaluation, you will gain exposure to a broad range of scientific, regulatory, and evidence-based writing activities, providing meaningful opportunities to expand your impact across the product lifecycle.

Responsibilities include, but are not limited to:

  • Review, evaluate, and summarize scientific literature relevant to the product portfolio.

  • Identify and report complaints, adverse events, and other reportable findings from published literature to Global Clinical and Regulatory stakeholders.

  • Develop responses to regulatory authority, audit, and submission-related inquiries.

  • Maintain and manage a database of peer-reviewed literature and clinical evidence.

  • Critically appraise, analyze, synthesize, and interpret clinical evidence from all the available sources.

  • Conduct comprehensive literature searches and perform a critical evaluation of clinical data and evidence.

  • Develop and maintain state-of-the-art assessments for product families in support of their intended use and regulatory requirements.

  • Create, update and maintain clinical evaluation plans, reports, and support documents for regulatory authorities.

  • Review and approve technical, clinical and regulatory documentation supporting device development and lifecycle management.

  • Collaborate with cross functional teams to ensure clinical evidence strategies align with regulatory, quality, and business objectives.

Successful candidates bring:

  • Strong scientific judgment and evidence synthesis expertise, with the ability to evaluate and integrate evidence from scientific literature, clinical studies, real-world data, post-market surveillance, and other sources into balanced, evidence-based conclusions regarding device safety, performance, and clinical benefit.

  • Relevant experience in medical devices, life sciences, clinical research, regulatory affairs, clinical evaluation, or scientific/medical writing, with a solid understanding of evidence appraisal, clinical research principles, and regulated product development.

  • A regulatory and benefit-risk mindset, including experience applying scientific evidence to support regulatory submissions, safety and performance assessments, risk management activities, or evidence-based decision-making in a regulated environment.

  • Learning agility, adaptability, and senior-level independence, with the ability to quickly develop expertise in new areas, navigate ambiguity, manage evolving priorities, proactively identify risks and gaps, and operate effectively with limited oversight.

  • Excellent communication, collaboration, and influence skills, with the ability to translate complex scientific information into clear, meaningful insights and drive alignment across cross-functional teams.

  • Leadership and mentoring capabilities, serving as a trusted scientific resource who leads complex initiatives that advance clinical evidence and evaluation practices.

Location: Rice Creek/Fridley, MN (Onsite)

Minimum Requirement (Basic Qualifications):

To be considered for this position, the following Basic Qualifications must be evident on your resume

  • Requires a Baccalaureate degree in life sciences, healthcare, engineering or related field and a minimum 7 years of relevant experience,

  • or advanced degree life sciences, healthcare, engineering or related field and a minimum of 5 years of relevant experience.

Nice To Have (Preferred Qualifications):

  • Advanced degree in a life sciences, healthcare, engineering, or related discipline (M.S., MPH, PharmD, PhD, MD, or equivalent) is preferred.

  • Experience authoring or contributing to clinical, regulatory, or scientific deliverables within the medical device or highly regulated life sciences industry.

  • Demonstrated ability to critically evaluate and synthesize complex evidence from scientific literature, clinical studies, real-world data, post-market surveillance, and other relevant sources to support evidence-based conclusions.

  • Strong understanding of clinical research methods, evidence appraisal, epidemiology, biostatistics, and/or clinical evaluation principles, with the ability to apply these concepts to support balanced, evidence-based conclusions.

  • Knowledge of global medical device regulations and standards, including EU MDR, MEDDEV 2.7.1 Rev. 4, ISO 14155, ISO 14971, and related guidance.

  • Experience supporting regulatory agency, notified body, or audit interactions.

  • Strong analytical, communication, project management, and stakeholder management skills, with the ability to influence across cross-functional teams.

  • Demonstrated success working independently in complex, fast-paced, highly regulated environments, with the learning agility, judgment, adaptability, and seniority to manage ambiguity, balance multiple priorities, quickly build expertise in new requirements or therapy areas, and guide evidence-based decision-making across cross-functional teams.

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.

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):$131,200.00 - $196,800.00This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

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, andSimple 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), andCapital 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 findhere 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.


What Medtronic employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom