Sr. Clinical Safety Specialist (Remote)

Work Flexibility: RemoteStyker Inari is seeking a Sr. Clinical Safety Specialist to ensure accurate, timely, and consistent safety assessments of adverse events across sponsored clinical studies and registries. This is a remote position based anywhere within the United States.As Sr. Clinical Safety Specialist, you will support the integrity and quality of clinical safety data across a portfolio of clinical studies and registries. This role focuses on consistent evaluation, documentation, and reporting of adverse events in alignment with global requirements while collaborating across study teams and external partners. You will contribute to the execution of safety processes throughout the clinical study lifecycle.What you will doReview adverse events, serious adverse events, and endpoint-related events across clinical studies to ensure accurate assessment and documentation.Prepare clinical safety narratives using source documents and study data, completing deliverables within defined timelines and quality standards.Collaborate with clinical sites and monitors to request, collect, and verify source documentation required for adjudication.Apply MedDRA coding to adverse events to ensure standardized classification and consistency across studies.Coordinate with study teams, medical monitors, and adjudication committees to support protocol-aligned safety reviews.Contribute to safety management plans for assigned protocols and support safety review meetings with documented findings.Monitor safety data quality by identifying discrepancies and implementing corrective actions to maintain completeness and accuracy.Maintain compliance with Good Clinical Practice and regulatory requirements through adherence to standard operating procedures and audit readiness.What you needRequiredBachelor’s degree2+ years of clinical research experienceExperience applying Good Clinical Practice standards in clinical trialsProficient with electronic databases used for clinical trials such as, Zelta, etc.PreferredBachelor's degree in life science or related field2-4 years of experience in medical device clinical trialsExperience with adverse event review, safety reporting, or pharmacovigilance processesKnowledge of MedDRA coding standardsPossesses exceptional attention to detail and strong analytical skills to accurately review CRFs, source documents, and evaluate safety data for quality and complianceBrings medical knowledge and preferably experience in clinical trials or medical devices to support informed decision-making and data integrity   United States of America Pay Ranges:USN: $83,300 - $138,800 USD AnnualUS5: $87,500 - $145,700 USD AnnualUS10: $91,600 - $152,700 USD AnnualUS15: $95,800 - $159,600 USD AnnualUS20: $100,000 - $166,600 USD AnnualUS30: $108,300 - $180,400 USD AnnualView the U.S. work location and transparency guide to find the pay range for your location.   Travel Percentage: 10%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.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.