Clinical Project Manager jobs in United States
cer-icon
Apply on Employer Site
company-logo

Globus Medical · 3 hours ago

Clinical Project Manager

Globus Medical is dedicated to improving the quality of life for patients with musculoskeletal disorders through innovative solutions. The Clinical Project Manager will be responsible for overseeing clinical investigation protocols, managing study sites, and ensuring compliance with regulatory requirements while maintaining project scope, timelines, and budgets.

Health CareManufacturingMedicalMedical DeviceWellness
check
H1B Sponsor Likelynote

Responsibilities

Serves as the primary point of contact, with oversight from leadership, for assigned studies, working with Product Development, Sales, Marketing, Regulatory Affairs, and Legal to communicate relevant updates accordingly through the life and closure of the study
Fosters relationships with physicians, sales representatives, and clinical teams to gain input into study design, evaluate study feasibility, and identify sites for study execution or data collection for the assigned study
Supports the design and review of all study documents for the assigned study, including the clinical study protocol, case report forms and subject questionnaires, informed consent form, electronic data capture (EDC) system, and other study tools
Supports the sponsor study start-up process by, including but not limited to, contributing to the conduct of the study kick-off meeting, negotiation and execution of agreements/budgets, and ensuring all qualification documents are executed and obtained
With oversight from leadership, supports the management of project budgets, communicates deviations from budget projections, and proposes solutions for budget deviations. Ensures timely processing of site payments for assigned study
Ensures site compliance with applicable regulatory requirements
Provides support to clinical investigators and site coordinators to resolve site-related issues
Ensures timely completion of patient enrollment and data collection in accordance with protocol requirements
Conducts remote and on-site monitoring including site qualification visits, site initiation visits, interim monitoring visits, and closeout visits, in compliance with standard operating procedures and expectations set by the governing regulatory authority
Supports the preparation, analysis, and review of clinical study data using basic comparative statistical techniques to support data interpretation and reporting
Supports generation of reports, conference abstracts, and journal publications in collaboration with leadership and investigators
Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies
Ensures compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to the role
Represents the company in a professional manner and upholds the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties

Qualification

Clinical trial conductFDAEU MDR knowledgeData managementMicrosoft OfficeStatistical softwareOral communicationWritten communicationTeamworkCustomer focus

Required

Bachelor's Degree with 2+ years' clinical experience in the Sciences / Engineering / Health Care / Management OR surrogate experience in Medical Device Clinical Affairs, Product Development, Marketing, and Management in a fast-paced environment
Experience with Microsoft Office applications, SPSS or other statistical software
Working knowledge of FDA and EU MDR requirements (ISO14155) for clinical trial conduct
Demonstrated ability and experience with clinical investigators to motivate, lead, and provide support to group towards rapid, compliant enrollment
Excellent oral and written communication skills
Ability to travel up to 10-30% of the time

Preferred

Previous publication history or contributions to peer-reviewed articles

Company

Globus Medical

company-logo
Globus Medical is a musculoskeletal implant manufacturer, driving technological advancements across a suite of spinal products.

H1B Sponsorship

Globus Medical 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 (24)
2024 (17)
2023 (13)
2022 (8)
2021 (9)
2020 (11)

Funding

Current Stage
Public Company
Total Funding
$128.52M
Key Investors
Clarus Ventures
2012-08-03IPO
2007-08-23Series E· $110M
2007-02-05Series D· $9.45M

Leadership Team

leader-logo
Norbert Johnson
CTO of Imaging, Navigation & Robotics
linkedin
leader-logo
Harri Hallila
Managing Director, International Advanced Technologies
linkedin
Company data provided by crunchbase