Registered Dietician in Columbus, OH

  • Title: Registered Dietician
  • Code: RCI-34342
  • RequirementID: 115871
  • Location: Columbus, OH 43219
  • Posted Date: 02/29/2024
  • Duration: 12 Months
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  Job Description

Schedule: Onsite 4 day and 1 work from home day.

  • Will be supporting a new team mostly based in the UK. Working hours will still be Eastern business hours.
  • Team is looking for candidates that have clinical background more than Med device or Pharma.
  • Looking for candidates with Bachelor’s preferred in Nursing or Dietitian.
Looking for a candidate with more of a nutrition background; a dietitian or someone with some nutrition science undergraduate work.

Duties:

  • As an individual contributor, with guidance from manager/team, functions to support medical safety team by collecting, assessing, processing adverse events for clinical or post-marketed products in compliance with applicable regulations, 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.
Responsibilities:
  • 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 completion of MSS related analyses, reports, and/or projects as assigned, e.g., ingredient and finished product assessments and/or medical safety assessments.
  • Coding cases using appropriate dictionary, searching and inputting data in electronic databases.
  • 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.
  • Presenting MSS related analyses, reports, and/or assessments orally and/or in writing within the department.
  • Assisting in the generation of medical justification content reviews/templates for MSS.
Skills:
  • 0-3 years related experience.
  • Some industry experience desirable.
  • Clinical knowledge to apply to adverse event data collection and/or medical/product assessments.
  • Computer proficient (Windows, Word, Excel) and proficient in specific adverse event databases (as applicable).
  • Able to present case data, medical and scientific data orally and in writing.
  • Clinical Monitor or Research Coordinator
Education:
  • Associates or Bachelor’s degree preferred in Healthcare or Science.
  • Will consider someone directly out of college.


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