Job Details

  • Title: Medical Monitor
  • Code: RCI-36711-1
  • Location: Summit New Jersey (NJ) 07901
  • Posted Date: 04/05/2021
  • Duration: 6 Months

  Job Description

Expertise Required:

  • MD or DO with experience in diabetes or at a minimum in internal medicine
  • A minimum of 10 years of industry experience
  • In depth knowledge of and experience as a medical monitor for clinical trials
  • Good verbal and written communication skills essential
  • Experience managing projects in a matrix environment, coordinating activities and adhering to tight timelines
  • Excellent written and verbal communication skills are required
  • Strong interpersonal skills including the ability to influence others
  • Strong leadership skills
  • Attend weekly update meeting with Client`s core team (PM, DM, stats)
  • Attend weekly meetings with CRO and/or other vendors
  • Help CRO respond to site and HA questions about the protocol
  • Monthly review of Jreview and CRO data listings and QNET lab data. Attend monthly safety meetings with CRO
  • Review daily lab alerts and SAEs. Communicate with CRO regarding follow-up.
  • Monthly review of protocol deviations
  • Attend and present at Investigator meetings
  • CRF review
  • Present study updates at CPT
  • Monthly participation in MST
  • DBL (final listing review, review of blinded TLF, review protocol deviations, participate in all DBL meetings)
  • CSR writing (review final TLFs, work with medical writer to review & revise CSR document, draft discussion and conclusions, participate in comment resolution meetings)
  • Topline results presentation
  • Other tasks may be required as determined during the project by Client