DUTIES: Assist in the coordination and administration of clinical studies from start-up to execution and close-out; Set-up and maintenance of eTMF and ISF, including document tracking in accordance with ICH-GCP and local requirements; create and/or imports clinical-regulatory documents into the Global Electronic Management System (e.g., ANGEL), ensuring compliance for regulatory documents. set up, populates, and accurately maintains information using tools (e.g., CTMS such as IMPACT, SharePoint, etc.) and support systems; Manage and contribute to coordination and tracking of study materials and equipment; Coordinate administrative tasks during the study process, audits, and regulatory inspections, according to company policies and SOPs; Interface with the Data Management Center and/or Data Management Enablement representatives to facilitate the delivery of study-related documents and materials. Must be willing to travel and/or relocate to work in various worksites throughout the US. No telecommuting.Send resume to Truminds Technologies Inc, 5899 Preston Rd, Suite 501, Frisco, Texas 75034.
SKILLS: eTMF, ISF, CTMS, IMPACT, SharePoint & ANGEL.
REQUIREMENTS: Master’s degree inPharmaceutical Sciences, Statisticswith 2 yearsof experiencein a job titlewith similar duties and skills.
SALARY: $108, 867.00/Year
HOURS: 40 hours/week, Mon- Fri, 9:00am – 5:00pm
JOB LOCATION: Truminds Technologies Inc.5899 Preston Rd, Suite 501, Frisco, Texas 75034.
CONTACT: Jagdish Ambre / Operations and HR Manager.
PHONE: 469-850-1383
