Collecting, assessing and processing adverse event information in a compliant and timely manner in order to meet applicable clilatory 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.
Skills
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
Seniority level
Entry level
Employment type
Full-time
Job function
Administrative
Industries
Staffing and Recruiting
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