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Study Hub/Contacts
Who to reach

Study contacts

Your first call for day-to-day study questions is your Worldwide Clinical Trials site manager. The NervGen team below is available for sponsor-level questions, escalations and anything about these communications.

NervGen

MV Marissa Volpe SVP, Clinical Development & Operations mvolpe@nervgen.com Sponsor escalations, and protocol or medical questions that need sponsor input.
AS Angela Skipper Sr. Clinical Trial Manager askipper@nervgen.com Site activation, monitoring oversight and study conduct.
JB Julianna Burke Clinical Trial Associate jburke@nervgen.com Documents on this hub, newsletter content and distribution lists.

Worldwide Clinical Trials

Site management and medical monitoring

Worldwide Clinical Trials runs site management, monitoring, safety reporting and IRB submissions for RESTORE on NervGen's behalf.

  • Site manager: named on your site contact sheet; first call for visits, queries and supplies.
  • Medical monitor: eligibility and safety questions, 24-hour line on your contact sheet.
  • Safety reporting: reporting windows and submission details are in Site Resources.
  • IRB submissions: local IRB packages are prepared and sent by the Worldwide regulatory team.
Contact details for Worldwide staff are kept on your site-specific contact sheet in the investigator site file rather than on this page, so that changes in CRO staffing never leave a stale number here.

Study mailbox

For anything that does not fit above, including questions about this hub, write to the study mailbox. It is monitored each business day by NervGen Clinical Operations.

Study mailbox: restorestudy@nervgen.com