TELA Bio

• Overseeing the administrative responsibilities and project management of TELA Bio’s clinical operations activities • Supporting the execution of company sponsored studies, investigator-initiated activities, and day-to-day clinical operation tasks • Support the set-up and have operational responsibility for the maintenance of the local electronic Trial Master File (eTMF) including document tracking in accordance with ICH-GCP and local requirements • Collaborate with Clinical Project Managers (CPM) during the document collection process • Maintain study documents ensuring template and version compliance • Ensure important documents under their responsibility are of quality and uploaded in a timely manner • Liaison/collaborate with Clinical Project Manager, Investigational Sites, Legal and Compliance to expedite and finalize contracts and amendments • Create, prepare, and deliver reports to various departments • Organize meetings and meeting schedules • Perform clerical duties, such as filing, faxing, answering phone calls, and responding to emails