• Snapboard
  • Activity
  • Reports
  • Campaign
Welcome ,

Chat with the recruiter

...Minimize

Hey I'm Online! Leave me a message.
Let me know if you have any questions.

Spec 1, Clinical Data

In Georgia / United States

Save this job

Spec 1, Clinical Data   

Click on the below icons to share this job to Linkedin, Twitter!
JOB TITLE:
Spec 1, Clinical Data
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
Covington Georgia / United States

JOB DESCRIPTION :
Description:


The Clinical Risk Specialist I will perform MDR/adverse event reporting, evaluate clinical use of product, analyze data to reduce occurrence/risk, and analyze adverse events/complaint trends.

This position will ensure that all product complaints are documented, investigated, and reported in compliance to applicable Quality Systems regulations, ISO requirements, FDA regulations, and Corporate, Division, and International policies and procedures.

Education and/or Experience:
Bachelor’s degree required. Nursing degree combined with three years of nursing/clinical experience. Preferred experience with FDA regulated industry in complaint handling and MDR/adverse event reporting. Experience with Microsoft Office. Preferred experience in complaint handling software and Excel (Pivot Tables and Charts).

See attached for full job description details.

Position Details

Jun 14, 2021
Health Care
S16204860892385604
Georgia / United States
Covington
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Spec 1, Clinical Data    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Description:


The Clinical Risk Specialist I will perform MDR/adverse event reporting, evaluate clinical use of product, analyze data to reduce occurrence/risk, and analyze adverse events/complaint trends.

This position will ensure that all product complaints are documented, investigated, and reported in compliance to applicable Quality Systems regulations, ISO requirements, FDA regulations, and Corporate, Division, and International policies and procedures.

Education and/or Experience:
Bachelor’s degree required. Nursing degree combined with three years of nursing/clinical experience. Preferred experience with FDA regulated industry in complaint handling and MDR/adverse event reporting. Experience with Microsoft Office. Preferred experience in complaint handling software and Excel (Pivot Tables and Charts).

See attached for full job description details.