Senior Clinical Research Associate/Monitor - home-based, South UK regi - Find My Rizq
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DOCS Global

Here at DOCS Global, we have entered right into a partnership to provide an extra full-time, everlasting home-based Independent Biopharma CRAs to be aligned with a top-10 multinational pharmaceutical and biopharmaceutical firm.Is this the position you’re searching for? If so learn on for extra particulars, and ensure to use right now.Your focus would be the administration of Biopharma scientific trials within the South UK area on a monitoring foundation.You will have to be well-versed within the position of an Independent CRA within the UK, together with expertise of the start-up course of.What is Offered; * Excellent Salary bundle * Permanent profession alternative, together with in depth coaching interval. * Home-based flexibilityThe Role and your Responsibilities; • To carry out all elements of CRA duties from web site choice, web site initiation, by to web site routine monitoring visits. • Contributes to Case Report Form (CRF) design and scientific trial doc improvement as they pertain to scientific monitoring actions (i.e. working manuals, monitoring tips, and many others.); • Involved in recruitment of potential Investigators, preparation of Independent Ethics Committee/ Independent Regulatory Board (IEC/IRB) submissions, notifications to regulatory authorities, translation of research associated documentation, organisation of conferences and different duties as instructed by the PM; • Negotiates investigator budgets and assists with the execution of web site contracts with help from the authorized division; • Oversees all elements of research web site administration to make sure top quality information leading to constantly low question ranges and in good Quality Assurance studies; • Establishes, updates, tracks and maintains research particular trial administration instruments/programs, and standing studies; • Communicates successfully with web site personnel, together with the Principal Investigator (PI), and firm administration to relay protocol/research deviations and guarantee well timed implementation of corrective actions; What is Required; • Degree (BA/BS/BSc) in life sciences or certified nurse preferable • At least 12/18 months CRA expertise gained throughout the business as a Clinical Research Associate (CRA) both in Clinical Research Organisation (CRO) or pharmaceutical business or investigational web site • Experience of scientific trial arrange processes • EDC working expertise • Full-time availabilityContact / to debate in additional element.#CRAjob

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