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Principal Clinical Study Manager
Job
Stryker
Remote
$157,350 Salary, Full-Time
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Job Description
Why join Stryker? Looking for a place that values your unique talents? Discover Stryker's award-winning culture. We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards
US Stryker employee benefits. Stryker is seeking a Principal Clinical Study Manager to join our Neurovascular Division. This is a remote position based anywhere within the United States. As the Principal Clinical Study Manager , you will lead the planning and execution of complex clinical studies that advance innovation in stroke care. You will collaborate with cross-functional teams, ensure compliance with regulatory standards, and drive operational excellence to deliver high-quality results. What You Need Lead cross-functional clinical project teams, setting study strategy, timelines, budgets, and performance expectations across multiple global trials. Design and develop clinical study protocols and investigational plans in collaboration with physician advisors and internal stakeholders. Ensure compliant execution of clinical studies aligned with IRB/EC requirements, global regulatory standards, and company policies. Own end-to-end study management, including budget development, cost control, and delivery of high-quality, ethical, and publishable results. Oversee site selection, qualification, monitoring, and close-out, while directing CRAs and resolving operational and site-level issues. Drive study start-up and execution activities, including contracts, site training, CRF design, data management coordination, and CRO oversight. Monitor study performance through metrics and reporting, implementing corrective actions and maintaining clear communication with sites and stakeholders. Support regulatory submissions (e.g., IDEs, amendments) and lead study reporting, from progress updates through final reports and publication. Required Bachelor's degree in science or health care related field 8+ years of relevant work experience in clinical research with minimum 4 years of clinical study management experience Experience in the Medical Device or Pharmaceutical industry Proven ability to manage complex study programs, budgets, schedules, and cross-functional teams Strong leadership, communication, and stakeholder management skills Preferred CCRP, ACRP, PMP, PgMP, or equivalent professional certification Experience leading cross-functional teams
- not to mention various social and recreational activities, all of which are location specific.
US Stryker employee benefits. Stryker is seeking a Principal Clinical Study Manager to join our Neurovascular Division. This is a remote position based anywhere within the United States. As the Principal Clinical Study Manager , you will lead the planning and execution of complex clinical studies that advance innovation in stroke care. You will collaborate with cross-functional teams, ensure compliance with regulatory standards, and drive operational excellence to deliver high-quality results. What You Need Lead cross-functional clinical project teams, setting study strategy, timelines, budgets, and performance expectations across multiple global trials. Design and develop clinical study protocols and investigational plans in collaboration with physician advisors and internal stakeholders. Ensure compliant execution of clinical studies aligned with IRB/EC requirements, global regulatory standards, and company policies. Own end-to-end study management, including budget development, cost control, and delivery of high-quality, ethical, and publishable results. Oversee site selection, qualification, monitoring, and close-out, while directing CRAs and resolving operational and site-level issues. Drive study start-up and execution activities, including contracts, site training, CRF design, data management coordination, and CRO oversight. Monitor study performance through metrics and reporting, implementing corrective actions and maintaining clear communication with sites and stakeholders. Support regulatory submissions (e.g., IDEs, amendments) and lead study reporting, from progress updates through final reports and publication. Required Bachelor's degree in science or health care related field 8+ years of relevant work experience in clinical research with minimum 4 years of clinical study management experience Experience in the Medical Device or Pharmaceutical industry Proven ability to manage complex study programs, budgets, schedules, and cross-functional teams Strong leadership, communication, and stakeholder management skills Preferred CCRP, ACRP, PMP, PgMP, or equivalent professional certification Experience leading cross-functional teams
Posting Date:
06/02/2026Posted Date:
06/02/2026 This role will be posted for a minimum of 3 days.United States of America Pay Ranges:
USN :
$118,000- $196,700 USD Annual US5 : $123,900
- $206,500 USD Annual US10 : $129,800
- $216,400 USD Annual US15 : $135,700
- $226,200 USD Annual US20 : $141,600
- $236,000 USD Annual US30 : $153,400
- $255,700 USD Annual View the U.