Vacancy expired!
MEDICAL MONITOR FOR CLINICAL TRIALS SUMMIT, NJ Project Description:
- 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 the Client.
- MD or DO with experience in diabetes or at a minimum in internal medicin.
- 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.
Vacancy expired!