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**Stryker Inari** is seeking a **Clinical Safety Specialist (Remote)** to ensure accurate, timely, and consistent safety assessments of adverse events across sponsored clinical studies and registries. This role is responsible for maintaining compliance with global safety reporting requirements throughout the clinical study lifecycle. The Clinical Safety Specialist will collaborate closely with internal teams—including Safety, Clinical Program Management, Data Management, Biostatistics, Scientific Communications, and Complaint Handling—as well as external CROs and study partners to uphold the highest standards of patient safety and enable access to advanced care.

What you will do:

+ Interact with clinical sites, field monitors to obtain and verify source data for safety event adjudication.

+ Review and code adverse events (AEs), serious adverse events (SAEs), and endpoint-related events using MedDRA, ensuring accuracy and consistency across studies.

+ Write safety narratives and support Safety Review meetings in alignment with the Safety Management Plan and regulatory requirements.

+ Collaborate with Safety Leadership, Adjudicators (Medical Monitors and Clinical Events Committee), and cross-functional teams to develop and execute clinical safety plans.

+ Ensure timely and compliant reporting of AEs/SAEs/UADEs/MAEs while maintaining adherence to SOPs, GCP, and regulatory standards.

+ Drive high-quality safety data collection to support scientific communications, clinical research, and statistical analysis strategies.

+ Proactively identify and resolve potential safety data issues, ensuring clear communication with sites and study teams.

+ Apply strong technical knowledge of products, clinical processes, and disease states to enhance safety oversight and functional excellence.

What you need:

Required

+ Bachelor’s degree

+ Minimum 2 years of experience in clinical research

+ Proficient with electronic databases used for clinical trials, such as, Zelta, etc.

+ Experience with Good Clinical Practices (GCP)

Preferred

+ Bachelor’s degree in life science

+ Possesses exceptional attention to detail and strong analytical skills to accurately review CRFs, source documents, and evaluate safety data for quality and compliance.

+ Brings medical knowledge and preferably experience in clinical trials or medical devices to support informed decision-making and data integrity.

83,300.00 to 180,400.00 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.

Position posted on 1/12/2025

Posted Date: 01/12/2026

This role will be posted for a minimum of 3 days.

Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.

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.