Job Description
Assist with the investigator recruitment activities utilizing phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites. May assist in identifying study sites by performing site feasibility and recruitment tasks. Schedules and attend internal and external meetings as required. Prepares Investigator Site Files including distribution to study sites (electronically or physically), coordination with shipping vendor, if required. Performs ongoing essential document collection and review, maintenance, and close-out activities, organizing and maintaining site level data in the trial master file (TMF) under general supervision ensuring that sponsor and investigator obligations are being met and are compliant with ICH/GCP guidelines and applicable local regulations.
Acts as site contact/liaison for study and site management issues including addressing questions, assists with managing study supplies, and may support offsite central monitoring activities. Escalates issues and risks as needed. Ensures timely and complete data entry by site in EDC or any other system that requires data entry.
About Precision for Medicine
Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process.