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CRA / Clinical Research Associate - Warsaw /office-based/

Posted on Mar 16, 2019 by Docs Global (Continental Europe)

Not Specified Poland
Research & Development
13 Mar 2019
Annual Salary
Job Summary DOCS has partnered with a highly prestigious organisation with one of the most robust pipeline within the industry. We have a great job opportunity for a Clinical Research Associates who are ready to further develop their career and enjoy working for a global organisation in their offices in Warsaw Roles & Responsibilities of the position The Clinical Research Associate (CRA) acts as a liaison between site staff and Pharmaceutical Company, working within Polish Affiliate supporting one or more clinical trial(s) in a development programme. CRA is responsible for clinical trial operational targets (KPIs) and ensuring the highest possible data quality in clinical trial(s). The position is based in Warsaw, reports to Clinical Trial Leader, Poland and will require travelling up to 60% of the time. Responsibilities o The primary point of contact between site staff and Client o Leadership of site management for the selection and initiation of sites as well as conduct and closing activities of the appointed studies in compliance with local regulations, ICH-GCP, Client procedures and protocol requirements to ensure data quality and study subject protection o Managing the site to meet patient recruitment rate and target o Delivery of results that have direct impact on the successful completion of the clinical programme o Communication about progress and critical issues that may impair trial progress to Local trial Manager (LTM) and/or Regional Trial Manager (RTM) Job Requirements oExperience as CRA in the pharmaceutical industry or CRO, preferably with a minimum of 6 months of on-site monitoring experience oAbility to build and maintain relationships with sites oExcellent communication and negotiation skills oAdequate English verbal and writing skills, e.g. enabling understanding of the protocol and study documents as well as writing monitoring reports oAbility to manage multiple priorities oTeam oriented personality with high degree of flexibility Remuneration & other details We offer: •Full time permanent employment •Car allowance or company car •Work in the unique organization in Warsaw To Apply: Please contact Dagmara Drozdowska, Recruitment Consultant at DOCS on or email your up-to-date CV to: About DOCS: DOCS provides global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical trial industry. Key words: Clinical Research Associate, CRA, Monitor, on-site monitoring, Study Conduct, Regulatory, Pharmaceutical, CRO, Pharma, Contract Research Organisation, Biotech, Medical Device, Health, Biotechnology, Chemistry, Permanent, Warsaw, Poland

Reference: 671584508