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
- Bachelors 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.
- $105500.00 - $173900.00 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 contractors legal duty to furnish information.
Required Experience:
Senior IC
Work Flexibility: Remote or Hybrid or OnsiteThe 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 en...
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
- Bachelors 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.
- $105500.00 - $173900.00 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 contractors legal duty to furnish information.
Required Experience:
Senior IC
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