EndereçoAre you an experienced Clinical Study Site Coordinator with strong study planning and coordination experience, advanced English skills, passionate about patient care and would you like to make a difference in the development of new medicines and scientific advances? Well, this opportunity may be right for you: As a full time On-Site study coordinator (12-month contract), you will be responsible for coordinating all trial-related activities at site in order to ensure recruitment targets are met, data entry onto the eCRF is performed at high standards, patients visits are performed as per protocolo requirements, among other duties. You will be responsible for: Collection of biological samples; Collection of vital signs; Medication administration supervision; Providing guidance to patients; Assistance to patients in filling out questionnaires; Performing abbreviated physical examination; Record of activities performed on paper and electronic systems; Manage regulatory and ethical submissions; Responsible for ensuring study is compliance with local and federal laws and regulations; Recruit and screen potential study participants; Create and/or maintain all documents and records related to the study; Act as a point of reference for study participants by answering questions and keeping them informed on the study progress; Manage the inventory of equipment and supplies related to the study and orders more as needed; Attend meetings, events and seminars in order to promote the study; Requirements & Skills: Minimum of 5 years of experience (recent) as study coordinator; Lifesciences background; Advanced English (Mandatory); Excellent written and verbal communication skills Superior organizational and time management skills Capable of working independently with minimal supervision and also as part of a team Skilled with standard computer programs including the MS Office suite Ability to speak a second language is an asset, but not required Understanding of medical terminology as well as standard clinical procedures and protocols Adaptability and reliability. What you will get in return: Above average market compensation; Well balanced workload; Opportunity to work in clinical trials with cutting edge new medicines and expand your experience; High-quality training and support. Only applicants within the requirements above will be considered. If you believe this is the right opportunity for you please send your CV to
