Stryker · 15 hours ago
Clinical Study Manager
United States
Full-time
Remote
Mid Level
$96K/yr - $160K/yr
4+ years expStryker is a company that offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics, and Spine to improve patient and healthcare outcomes. The Clinical Study Manager is responsible for the operational management of clinical studies, ensuring compliance and high data quality while collaborating with cross-functional teams.
BiotechnologyHealth CareLife ScienceMedicalMedical Device
Responsibilities
Manage the day‑to‑day operational execution of clinical studies (IDE, post‑approval, post‑market, feasibility, marketing, and investigator‑initiated)
Contribute to study design and planning, including protocols, amendments, CRFs, monitoring plans, and operational procedures
Ensure clinical study activities comply with regulatory requirements, internal processes, and data management standards
Oversee study startup through close‑out, maintaining accurate and complete Trial Master File documentation
Coordinate and support site monitoring activities, ensuring data quality, consistency, and timely issue resolution
Lead data collection, validation, and system testing activities (e.g., eCRF/UAT) to support high‑quality study outputs
Track enrollment, timelines, milestones, risks, and deliverables; maintain study dashboards and reports
Partner with cross‑functional teams to identify and mitigate study risks and adapt to changes in scope or priorities
Manage Investigator‑Initiated and Stryker‑sponsored studies, including contracts, deliverables, and registry/database engagement
Collaborate with Legal and Finance to ensure compliant contract execution and investigator reimbursement
Drive evidence generation by supporting analysis, publication, and presentation of study results
Independently manage multiple studies while prioritizing workload and delivering results aligned with Stryker’s research strategy
Qualification
Required
Bachelor's level degree or equivalent in science or health care field with at least 4 years of relevant clinical research experience, preferred in clinical study management
Demonstrated success in assisting in solving complex strategies across multiple functions within the department in support of conducting multiple global clinical trials across multiple franchises
Demonstrated understanding of laws, regulations, standards, and guidance governing the conduct of clinical studies, as well as preparation of clinical documentation in support of regulatory submissions
Preferred
Experience in Device or Pharmaceutical industry
Clinical research or project management certification (e.g., CCRP, ACRP, PMP)
Strong communication and presentation skills (articulate and persuasive)
Strong organizational and project management skills with a high sense of attention to detail
Benefits
Medical and prescription drug insurance
Dental insurance
Vision insurance
Critical illness insurance
Accident insurance
Hospital indemnity insurance
Personalized healthcare support
Wellbeing program
Tobacco cessation program
Health Savings Account (HSA)
Flexible Spending Accounts (FSAs)
401(k) plan
Employee Stock Purchase Plan (ESPP)
Basic life and AD&D insurance
Short-term disability insurance
Company
Stryker
Stryker is a medical technology company that offers products and services in orthopaedics.
10001+ employees
H1B Sponsorship
Stryker has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (105)
2024 (76)
2023 (63)
2022 (78)
2021 (57)
2020 (77)
Funding
Current Stage
Public CompanyTotal Funding
unknown1990-01-02IPO
Leadership Team
Kevin Lobo
Chair & CEO
Glenn S. Boehnlein
Chief Financial Officer and Vice President
Recent News
GlobeNewswire News Room
2025-02-11
Company data provided by crunchbase