Supports interface with the oncology and U.S. clinical team members, clinical operations, scientific operations, regulatory affairs, drug supply, data management, finance, quality, compliance, and other relevant functional areas
Updating appropriate databases(contact information), CTMS system, tracking, sending out info to sites, e-mailing sites, payments, right hand person to Trial Lead, takes minutes, sets up meetings, reg doc collections (familiar with 1572s, IRB documents, trial master files content)
Maintain project files including: ethics committee approvals; curricula vitae of investigators and study personnel; clinical investigators brochure; protocols; case report forms instructions;
Support Trial Leads in liaising with study investigators, site research staff, and field based colleagues to support clinical studies.
Organize investigator’s start-up meeting and study site initiation meetings.
Support study enrollment efforts, planning for inv meetings.
Bachelor's degree in a science related field
Minimum 1-2 years of clinical research experience or equivalent
Source: Job Diva – Job Listing