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Stryker

Stryker

via Indeed

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Clinical Program Manager (Remote)

Anywhere
Full-time
Posted 1/10/2026
Verified Source
Key Skills:
Clinical trial management
Regulatory compliance (GCP, GLP)
Project management

Compensation

Salary Range

$139K - 232K a year

Responsibilities

Lead all aspects of clinical trial management from planning to closure, collaborating with cross-functional teams and CROs.

Requirements

8+ years of clinical research experience, with at least 4 years in clinical study management, and familiarity with GCP, GLP, and global regulatory pathways.

Full Description

What you will do As a Clinical Program Manager, you will lead all aspects of clinical trial management across the study life cycle—from planning to execution to closure. You will collaborate with cross-functional teams and CRO partners to deliver high-quality evidence supporting regulatory approvals, reimbursement, and market expansion. • Design, plan, and implement clinical trials to demonstrate safety, efficacy, and quality outcomes for Inari products globally. • Define study objectives, strategy, scope, and timelines to meet business needs. • Partner with internal and external stakeholders to support regulatory approvals and market access. • Develop Clinical Investigational Plans and supporting documents (IB, PIC, Safety Plan, Data Management Plan). • Provide clinical training for investigators, site staff, CRO partners, and internal teams. • Oversee safety reviews and validate clinical data for analysis and publications. • Manage CRO selection, oversight, and site visits to ensure compliance with CIP and objectives. • Prepare interim and final reports, lead investigator meetings, and coordinate publication initiatives. • Develop and manage budgets for assigned clinical studies. • Follow and improve Clinical SOPs, systems, and processes for quality study management. What you need • Bachelor’s degree in science or health care related field. • 8 years of relevant clinical research experience with minimum 4 years of clinical study management experience. • Experience with Good Laboratory Practice (GLP) and Good Clinical Practice (GCP). • Strong project management skills and ability to influence cross-functional teams. • Excellent communication, organizational, and analytical skills. Preferred • Master’s degree with a demonstrated research background. • Clinical research or project management certification (eg, CCRP, ACRP, PMP). • Experience in medical device clinical trials. • Familiarity with global regulatory and reimbursement pathways. • Experience leading cross functional teams • $139,200.00 - 231,800.00 USD Annual salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors. • ​Posted: January 09, 2026 Posted Date: 01/09/2026 This role will be posted for a minimum of 3 days.

This job posting was last updated on 1/15/2026

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