Senior Clinical Research Associate

My client is a mid:sized CRO and due to a number of extra projects in which they have taken on, starting this year, they are rapidly looking to expand their clinical team across Europe with a number a different levelled CRAs.Responsibilities:Perform on:site monitoring visits as well as site identification, feasibility and selection as requiredResponsible for evaluating, initiating, monitoring and closing out clinical study sitesEnsure clinical projects are conducted, recorded, and reported in accordance with theproject protocolComply with Good Clinical Practice (GCP), Company SOPs and all applicable regulatory requirementsProvide ongoing updates and support to project managementRequirements:At least 2 years of experience with independent monitoring in PolandPrevious CRO experienceExcellent knowledge of ICH:GCP and any other relevant, local regulatory requirementsAbility to travel 25 of the timeFluent in English and PolishIf you're interested in a new challenge for the new year, then get in touch today to discuss this role in further details: