Clinical Trial Coordinator I/II - FSP

Job Title: Clinical Trial Coordinator I/II - FSP Job Location: Remote, North Carolina, USA Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Trial Coordinator I/II - FSP – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. Role-related skills Excellent technical/IT skills. Able to understand the impact of technology on studies and to use and develop computer skills while making appropriate use of Client systems/software Knowledge of relevant operational procedures, systems and quality guidelines regarding clinical studies Able to work independently as well as in a team. Professional attitude with good customer focus (internal and external) Role Responsibilities Maintain up to date participating center’s information (including all contact details, contracts and reports). Responsible for preparing the Investigator and Sponsor files with essential documents for the initiation of sites participating in clinical studies. Assist Client study staff with maintaining the sponsor files during the life of the study. Responsible for archiving at the end of study in accordance with relevant Client SOPs, policies and local regulatory requirements. Input and oversee Client clinical study tracking systems Proactively identifies issues and raises them to Client study staff to take necessary corrective action to ensure smooth and rapid progress of studies. Assist in the planning, logistics and preparation of local Investigator meetings (travel arrangements, assist with preparation and distribution of study related presentation material etc.) Responsible for working with the Client Study staff for the management of study materials, non-IMP and IMP supplies - distribution, ordering, tracking, stora