.**Primary Functions**:You will perform a dual function as a clinical research coordinator and a lab assistant. You will assist and coordinate clinical research projects, dealing with medical staff and patients, tracking, organizing, and preparing samples in the lab for storage and shipment, and also doing all lab paperwork for different research projects.**Lab Assistant duties and responsibilities**Prepare samples/specimens for storage and shipmentFill shipment manifestsPerform daily quality control checksPrepare reports with reliable dataUse latest methodologies and best practicesAdhere to correct procedures and policiesDocument all activitiesMaintain and track resultsMaintain cleanliness, orderliness and suppliesHelp with administrative tasks**Tasks as a Clinical Research Coordinator**:- Assist in the planning, implementation, and management of clinical trials according to study protocols, FDA guidelines, and Good Clinical Practice (GCP) standards.- Recruit and screen potential study participants, ensuring they meet eligibility criteria and obtaining informed consent.- Schedule and conduct study visits, collect and document data, and maintain accurate and complete research records.- Monitor study progress, identify potential issues, and work proactively to resolve any challenges that arise during the research process.- Coordinate with research team members, healthcare professionals, and external partners to facilitate study procedures and ensure the timely completion of research milestones.- Assist with the preparation of regulatory documents and submissions for Institutional Review Board (IRB) approval and other regulatory bodies as required.- Ensure compliance with all relevant regulatory guidelines, study protocols, and safety procedures throughout the research process.- Collaborate with data management teams to ensure accurate and timely data entry and maintenance.- Prepare and maintain study-related supplies and equipment, ensuring they are readily available for research activities.- Monitor and manage adverse events and communicate them to relevant stakeholders as appropriate.- Stay updated on industry best practices, guidelines, and regulatory changes related to clinical research.**Qualifications and requirements**Bachelor's degree in health related areas. Químico, Químico Farmacéutico Biólogo (QFB), Químico Clínico Biólogo (QCB), Químico Bacteriólogo Parasitólogo (QBP), Biotecnología y Genómica (LBG), Biología, Ingeniería en Biotecnología, Ingeniería Biomédica, and other similar or related degrees.Fluent in English.Outstanding work ethic, detail-oriented, thorough, punctual and extremely well organized.You must be reliable, motivated, looking for work within a research environment and have a flexible attitude to work and schedules.Demonstrated ability to interact with different professional levels of the medical and laboratory community