Overview

Safety and Pharmacovigilance Specialist – USMD Job at Technical Resources International, Inc. – 2.8 Bethesda, MD

Job Details

Full-timeEstimated: $49,000 – $73,000 a year4 hours ago

Qualifications

  • Clinical trials
  • Clinical research

Full Job Description

Responsibilities
Performs various tasks in support of clinical research including adverse event analysis and processing; serious adverse event reconciliation; preparation of IND safety reports for submission to the FDA; safety document or data analysis; clinical trial site support; reporting, collecting, and sharing of results and issues around adverse event reports both for currently marketed drugs as well as those in the experimental stages of development; assists in the preparation of new drug application safety updates, investigational new drug safety reports, investigator communication, product labeling/package inserts, and other reports as necessary; may review experimental protocols and informed consent documents; and prepares, reviews, and edits presentations regarding safety issues.

Recommended Skills

  • Ich Guidelines
  • Clinical Research
  • Good Clinical Practices (Gcp)
  • Med Dra
  • Oncology
  • Presentations

Job Snapshot
Employee Type
Full-Time
Location
Bethesda, MD
Job Type
Biotech
Experience
Not Specified
Date Posted
09/27/2021
Job ID
217/114/552

Job Type: Full-time

Work Location: Multiple Locations

About the Company

Company: Technical Resources International, Inc. – 2.8

Company Location:  Bethesda, MD

Estimated Salary:

About Technical Resources International, Inc. - 2.8