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6 Apr 2021

Temporary Clinical Medical Monitor (21-08927)

iris.chen@axelon.com – Posted by iris.chen@axelon.com Summit, New Jersey, United States

Job Description

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 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

How to Apply

Please send your updated resume to iris.chen@axelon.com

Job Types: Temporary.

Job expires in 80 days.

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