Clinical Project Manager Green Card Jobs
Clinical Project Manager roles at U.S. pharmaceutical, biotech, and CRO employers qualify for EB-2 and EB-3 green card sponsorship through the PERM labor certification process. Your employer files the I-140 immigrant petition after PERM is certified, putting you on the path to permanent residency rather than a temporary work status.
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We anticipate the application window for this opening will close on - 5 May 2026
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
As a Principal Clinical Project Manager, you will support the Clinical Project Management Office (PMO) by managing and executing a portfolio of clinical projects, including post-market clinical studies and related initiatives.
This role is focused on driving consistent execution, maintaining operational processes, and ensuring visibility across multiple active projects. Success in this role requires strong project management expertise combined with a solid understanding of clinical research processes, requirements, and cross-functional dependencies.
You will leverage established PMO frameworks, tools, and best practices to coordinate work, monitor progress, and support delivery across cross-functional clinical teams.
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. This position is remote to enhance our competitive edge and expand our cross-functional collaboration efforts.
Responsibilities may include the following and other duties may be assigned.
Project Execution & Oversight
- Manage multiple concurrent clinical projects from initiation through completion
- Own project scope, schedule, and execution across assigned initiatives
- Develop and maintain detailed project plans, timelines, and dependencies using tools such as Smartsheet
- Track progress, identify risks, and ensure alignment to study milestones and deliverables
- Ensure consistent execution of established PMO processes and clinical project standards
Operational Management
- Oversee day-to-day operational aspects of assigned projects
- Serve as liaison between clinical teams, functional partners, and leadership
- Drive alignment across stakeholders and ensure timely issue resolution
- Support resource coordination and workload visibility across projects
Reporting & Visibility
- Maintain project dashboards, status reporting, and portfolio tracking
- Provide clear, consistent updates on project health (timeline, milestones, risks)
- Deliver updates to stakeholders and leadership to support decision-making
- Ensure data accuracy and transparency across reporting tools
Risk Management & Problem Solving
- Proactively identify project risks, issues, and dependencies
- Lead mitigation planning and drive resolution across cross-functional teams
- Escalate issues as appropriate and ensure timely follow-through
Process Adherence & Continuous Improvement
- Apply established PMO methodologies, tools, and clinical workflows
- Identify opportunities for incremental process improvements
- Support adoption and consistent use of standard tools and practices
Cross-Functional Leadership
- Lead and coordinate work across cross-functional teams in a matrixed environment
- Influence stakeholders without direct authority to drive project outcomes
- Provide guidance or mentorship to less experienced team members as needed
Must Have (Minimum Requirements)
- Bachelor’s degree
- 7+ years of experience in project management, clinical research, operations, or related field
- Experience managing multiple complex, cross-functional projects in a matrixed environment
- Experience supporting or working within clinical research (e.g., post-market, IDE, or regulated environment)
Nice to Have
- Strong ownership of project delivery across scope, schedule, risks, and execution for multiple concurrent initiatives
- Experience managing complex, cross-functional projects in a regulated or medical device environment, including familiarity with the clinical study lifecycle
- Proficiency with project management tools (e.g., Smartsheet or similar), including detailed project planning, dependency management, and tracking
- Demonstrated strength in risk identification, mitigation, and issue resolution, with the ability to escalate effectively
- Experience with portfolio-level reporting, dashboards, and executive-ready status updates within a PMO or structured delivery environment
- PMP certification (or equivalent experience) and ability to influence, communicate with stakeholders, and mentor junior team members
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.
Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued.
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): $116,000.00 - $174,000.00
This 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, 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.
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.

We anticipate the application window for this opening will close on - 5 May 2026
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
As a Principal Clinical Project Manager, you will support the Clinical Project Management Office (PMO) by managing and executing a portfolio of clinical projects, including post-market clinical studies and related initiatives.
This role is focused on driving consistent execution, maintaining operational processes, and ensuring visibility across multiple active projects. Success in this role requires strong project management expertise combined with a solid understanding of clinical research processes, requirements, and cross-functional dependencies.
You will leverage established PMO frameworks, tools, and best practices to coordinate work, monitor progress, and support delivery across cross-functional clinical teams.
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. This position is remote to enhance our competitive edge and expand our cross-functional collaboration efforts.
Responsibilities may include the following and other duties may be assigned.
Project Execution & Oversight
- Manage multiple concurrent clinical projects from initiation through completion
- Own project scope, schedule, and execution across assigned initiatives
- Develop and maintain detailed project plans, timelines, and dependencies using tools such as Smartsheet
- Track progress, identify risks, and ensure alignment to study milestones and deliverables
- Ensure consistent execution of established PMO processes and clinical project standards
Operational Management
- Oversee day-to-day operational aspects of assigned projects
- Serve as liaison between clinical teams, functional partners, and leadership
- Drive alignment across stakeholders and ensure timely issue resolution
- Support resource coordination and workload visibility across projects
Reporting & Visibility
- Maintain project dashboards, status reporting, and portfolio tracking
- Provide clear, consistent updates on project health (timeline, milestones, risks)
- Deliver updates to stakeholders and leadership to support decision-making
- Ensure data accuracy and transparency across reporting tools
Risk Management & Problem Solving
- Proactively identify project risks, issues, and dependencies
- Lead mitigation planning and drive resolution across cross-functional teams
- Escalate issues as appropriate and ensure timely follow-through
Process Adherence & Continuous Improvement
- Apply established PMO methodologies, tools, and clinical workflows
- Identify opportunities for incremental process improvements
- Support adoption and consistent use of standard tools and practices
Cross-Functional Leadership
- Lead and coordinate work across cross-functional teams in a matrixed environment
- Influence stakeholders without direct authority to drive project outcomes
- Provide guidance or mentorship to less experienced team members as needed
Must Have (Minimum Requirements)
- Bachelor’s degree
- 7+ years of experience in project management, clinical research, operations, or related field
- Experience managing multiple complex, cross-functional projects in a matrixed environment
- Experience supporting or working within clinical research (e.g., post-market, IDE, or regulated environment)
Nice to Have
- Strong ownership of project delivery across scope, schedule, risks, and execution for multiple concurrent initiatives
- Experience managing complex, cross-functional projects in a regulated or medical device environment, including familiarity with the clinical study lifecycle
- Proficiency with project management tools (e.g., Smartsheet or similar), including detailed project planning, dependency management, and tracking
- Demonstrated strength in risk identification, mitigation, and issue resolution, with the ability to escalate effectively
- Experience with portfolio-level reporting, dashboards, and executive-ready status updates within a PMO or structured delivery environment
- PMP certification (or equivalent experience) and ability to influence, communicate with stakeholders, and mentor junior team members
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.
Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued.
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): $116,000.00 - $174,000.00
This 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, 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.
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.
See all 315+ Clinical Project Manager jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Project Manager roles.
Get Access To All JobsTips for Finding Green Card Sponsorship as a Clinical Project Manager
Align your credentials to EB-2 requirements
A master's degree in clinical research, public health, or a life science field positions you for EB-2. If you hold a bachelor's plus five or more years of progressive CRO or sponsor-side experience, document that progression carefully before targeting EB-2 roles.
Target employers with active PERM filing history
Pharmaceutical companies, large CROs, and health systems file PERM petitions regularly for Clinical Project Managers. Use Migrate Mate to filter by employers with documented EB-2 and EB-3 sponsorship history for this specific role, not just general H-1B filers.
Understand the PERM prevailing wage before negotiating
DOL sets the prevailing wage for your role by location and experience level. Run your job title and metro area through the OFLC Wage Search before accepting an offer so you know the wage floor your employer must certify before filing.
Clarify sponsorship timing during the offer stage
PERM requires your employer to complete recruitment and DOL audit preparation before filing. Ask during final-round interviews whether the company uses in-house immigration counsel or outside firms, and what their typical PERM initiation timeline looks like post-hire.
Verify your role qualifies as a specialty occupation
Check the O*NET profile for Clinical Project Manager to confirm the standard educational and skill requirements DOL and USCIS use to evaluate PERM petitions. Roles with inconsistent degree requirements across employers can face additional scrutiny at the labor certification stage.
Prepare a detailed employment history for the I-140 stage
After PERM is certified, USCIS reviews your I-140 petition for evidence that you meet the stated job requirements. Gather reference letters, performance reviews, and project documentation from previous CRO or sponsor roles before your employer's attorney begins the I-140 package.
Clinical Project Manager jobs are hiring across the US. Find yours.
Find Clinical Project Manager JobsClinical Project Manager Green Card Sponsorship: Frequently Asked Questions
Do Clinical Project Manager roles typically qualify for EB-2 or EB-3 green card sponsorship?
Both categories apply, depending on your degree and experience. EB-2 fits candidates with a master's degree or a bachelor's degree plus substantial progressive experience in clinical operations. EB-3 covers professionals with a bachelor's degree in a relevant life science or health field. Most large CROs and pharmaceutical sponsors file under whichever category matches your background, and some will file both concurrently to protect your priority date.
How does the green card process differ from H-1B sponsorship for this role?
H-1B is a temporary work visa requiring renewal every three years, subject to the annual lottery cap. EB-2 and EB-3 green card sponsorship through PERM leads to permanent residency with no cap at the petition level. The tradeoff is time: PERM labor certification alone can take 12 to 18 months before USCIS even receives the I-140. For nationals of countries with long visa backlogs, the total wait can extend further, but the outcome is permanent status rather than a renewable temporary authorization.
What does the PERM labor certification process require from my employer?
Your employer must conduct a DOL-supervised recruitment campaign to demonstrate no qualified U.S. workers are available for your specific position. That includes mandatory job postings, documentation of applicant outreach, and a prevailing wage determination filed with DOL. The recruitment window, documentation period, and filing timeline typically span six to twelve months before DOL certifies the application and the employer can proceed to the I-140 petition with USCIS.
How do I find Clinical Project Manager jobs where the employer is willing to sponsor a green card?
Migrate Mate lets you search specifically for Clinical Project Manager roles with employers that have a documented history of EB-2 and EB-3 sponsorship, so you're not relying on job descriptions that vaguely mention visa support. Filtering by sponsorship type and role at the start of your search saves significant time and avoids employers who sponsor H-1B but have never initiated a PERM filing.
Can I change employers after my PERM is certified but before I receive my green card?
Yes, under AC21 portability rules, you can change to a same or similar job after your I-140 is approved and your I-485 has been pending for 180 days or more. For Clinical Project Managers, a move to a comparable role at a different sponsor or CRO within clinical operations generally qualifies. Your immigration attorney should review the new role against your approved petition's job description before you make the switch.
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