Clinical Trial Medical/ Safety Reviewer

Job Description:

• Pay: $26-$27/hr 
• Collecting, assessing and processing adverse event information in a compliant and timely manner in order to meet applicable regulatory requirements. 
• Coding cases using appropriate dictionary, searching and inputting data in electronic databases.
• Generating, tracking and resolving adverse event follow-up/distribution correspondence; managing adverse event reports from initial cases and follow-up.
• 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.
• Presenting MSS related analyses, reports, and/or assessments orally and/or in writing within the department.
• 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.
• Assisting in the generation of medical justification content reviews/templates for MSS.
• Assisting in the evaluation and establishment of nutrient specifications (minimum and maximum) during the process of formula development.  Uses IOM and DRIs and other nutrient guideline data to assess product development formulations and specifications.

Last updated on May 23, 2023