Medical Reviewer Jobs

Job Title: Medical Reviewer

Location: Columbus, Ohio (100% ONSITE)

Duration: 12-Month Contract (with the possibility to extend)

Benefits: Medical, Dental, and Vision

Summary

As an individual contributor, with guidance from the manager/team, functions to support medical safety team by collecting, assessing, and processing adverse events for clinical or post-marketed products in compliance with applicable regulations, and guidelines, researching, assessing, and summarizing nutrition and medical information as well as safety issues concerning foods or products and, by supporting clinical study teams with safety-related aspects and issues.

Duties / Expectations of Role

• Assisting in the generation of medical justification content reviews/templates for MSS.
• Coding cases using appropriate dictionary, searching and inputting data in electronic databases.
• Presenting MSS-related analyses, reports, and/or assessments orally and/or in writing within the department.
• Assisting in the completion of MSS-related analyses, reports, and/or projects as assigned, e.g., ingredient and finished product assessments and/or medical safety assessments.
• Researching, organizing, and assimilating clinical, safety, and/or toxicology information to support medical safety assessments, clinical study related safety reports, safety fact sheets and chemical approvals.
• Collecting, assessing and processing adverse event information in a compliant and timely manner in order to meet applicable regulatory requirements.
• Generating, tracking and resolving adverse event follow-up/distribution correspondence; managing adverse event reports from initial cases and follow-up.

Mandatory Requirements

• Computer proficient (Windows, Word, Excel) and proficient in specific adverse event databases (as applicable).
• Clinical knowledge to apply to adverse event data collection and/or medical/product assessments.
• 0-3 years related experience (Some industry experience desirable.)
• Able to present case data, medical and scientific data orally and in writing.
• Education: Associates or Bachelor’s degree preferred in Healthcare or Science. Will consider someone without a degree but they must have Clinical research/healthcare working experience.
• Clinical Monitor or Research Coordinator