~43m ago
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Director, Post Market Surveillance and Clinical Affairs

United StatesUnited States·GainesvilleFull Timeexecutive
OtherClinical
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Quick Summary

Overview

Leads the integrated Post Market Quality Assurance and Clinical Affairs functions, ensuring a compliant,

Technical Tools
OtherClinical
Leads the integrated Post Market Quality Assurance and Clinical Affairs functions, ensuring a compliant, effective QMS; timely identification and management of post-market signals; and development of clinical evidence supporting product safety, performance, and lifecycle decisions. Key areas include: 
  • Post-market surveillance, complaints, vigilance, MDRs, recalls, field actions, and EUDAMED reporting 
  • Clinical strategy, evidence planning, evaluations, literature reviews, and state-of-the-art assessments 
  • Post-market clinical follow-up (PMCF) planning and reporting 
  • Clinical investigations, external research, and clinical support for submissions, claims, and risk management

Location & Eligibility

Where is the job
Gainesville, United States
On-site at the office
Who can apply
US

Listing Details

First seen
September 29, 2026
Last seen
September 29, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
55%
Scored at
September 29, 2026

Signal breakdown

freshnesssource trustcontent trustemployer trust
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Director, Post Market Surveillance and Clinical Affairs