Senior Clinical Project Manager (Remote) at Stryker - Poland

Jersey City, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

08 Feb, 26

Salary

173900.0

Posted On

10 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Project Management, Regulatory Compliance, Study Design, Data Integrity, Interpersonal Skills, Attention to Detail, Publication Planning, Stakeholder Communication, Clinical Evidence Generation, Investigator Initiated Studies, Protocol Development, Market Access, Product Development, Audit Support, Key Opinion Leaders

Industry

Medical Equipment Manufacturing

Description

Work Flexibility: Remote or Hybrid or Onsite The Senior Clinical Project Manager (Remote) assists in global clinical evidence planning, clinical study design, and communication with assigned business units. The position contributes to the Clinical Research team activities for designated projects and ensures patient safety, quality and integrity of data, compliance with relevant SOPs and regulatory requirements and completes studies on-time and on-budget. What you will do Works closely with key internal (Marketing, R&D, Market Access, Product Development) and external stakeholders (surgeon researchers) to develop global clinical evidence generation plans to support the various needs of the business (e.g., regulatory filings, supporting claims). Maintains relationships with Key Opinion Leaders in support of Clinical Affairs activities. Manage assigned Investigator Initiated Study proposals, reviews, and conduct. Supports the development of publication plans and their execution in combination with relevant internal and external resources. Supports and helps manage creation of publication summaries and dissemination of this information. Supports Clinical Research team, sometimes serving as the Clinical representative, interactions with regulatory authorities, notified bodies and during audits. Supports, sometimes serves as the point person, communicating project status updates, resource needs, and other information for assigned business units and product lines. Supports study design processes, including protocol development, while working closely with the Clinical Operations and Clinical Data Sciences teams. What you need Bachelor’s degree required; in a health sciences; preference for degrees in biological sciences, engineering, or related medical/scientific field preferred. 6+ years’ experience directly supporting clinical device research or similar experience in a medical device scientific area. Understanding of industry clinical research regulations and best practices (e.g., ISO 14155, ICH GCP). Preferred Excellent interpersonal skills and the ability to work well independently as well as with co-workers, peers, supervisors, and external customers. High attention to detail and accuracy. $105,500.00 - $173,900.00 USD salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors. Posted: October 21, 2025 Travel Percentage: 20% Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces! For more information, visit: www.stryker.com Work Flexibility Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location. Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based. Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category. Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.

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Responsibilities

The Senior Clinical Project Manager assists in global clinical evidence planning and study design while ensuring compliance with regulatory requirements. They manage relationships with stakeholders and support the Clinical Research team in various project activities.