Clinical Study Manager (Remote)

Stryker • Portage, MI

109d • $87,600 - $186,700 • Remote

About The Position

Stryker is hiring a Clinical Study Manager to support our Medical Division. In this role you will be responsible for executing the clinical evidence strategy for medical devices, and support the development of this strategy, to enable new and continued global market access.

Requirements

• Bachelor's degree, preferably with Health Sciences or related technical field.
• 4+ years of relevant clinical research experience, preferred in clinical study management.

Nice To Haves

• Experience in the Medical Device Industry
• Knowledge of Digital Health technologies and trends
• Advanced degree (MSc, PhD) in health sciences, biomedical engineering, health outcomes research.
• Clinical research or project management certification (e.g., CCRP, ACRP, PMP).

Responsibilities

• Partner with cross-functional teams (e.g., Marketing, R D/NPD) to develop short- and long-term clinical evidence strategies, providing scientific expertise to guide business decisions.
• Develop and execute clinical regulatory strategies to support global market access, including authoring clinical sections of regulatory submissions and evaluations.
• Lead all aspects of clinical research: study design, execution, reporting, budgeting, contracting, monitoring, and ensuring compliance with Good Clinical Practice (GCP).
• Define and implement publication strategies, including manuscripts, conference presentations, white papers, and promotional materials, support customer publication efforts.
• Serve as Stryker's liaison with CROs, data vendors, medical writers, and other external partners to ensure scalable and high-quality clinical support.
• Manage clinical study documentation and submissions (e.g., EU MDR, IDE, IRB), supporting claims development that require clinical validation.
• Support the development and maintenance of procedures and systems (e.g., eTMF, CTMS) to ensure effective management of clinical studies and evaluations in compliance with global regulations.
• Generate clinical data aligned with business strategy through pre- and post-market trials, efficacy studies, registries, surveys, and literature reviews.

Benefits

• $87,600.00 - $186,700.00 salary plus bonus eligible + benefits.
• Individual pay is based on skills, experience, and other relevant factors.

What This Job Offers

• Career Level: Mid Level
• Industry: Miscellaneous Manufacturing
• Education Level: Bachelor's degree