Clinical Research Associate/Monitor - home-based - 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.A excessive variety of candidates might make purposes for this place, so make certain to ship your CV and utility by means of as quickly as potential.Your focus would be the administration of Biopharma medical trials within the North-West on a monitoring foundation.You will must be well-versed within the function of an Independent CRA, together with expertise of the start-up course of.What is Offered; * Excellent Salary package deal * Permanent profession alternative, together with intensive coaching interval. * Home-based flexibilityThe Role and your Responsibilities; • To carry out all facets of CRA duties from website choice, website initiation, by means of to website routine monitoring visits. • Contributes to Case Report Form (CRF) design and medical trial doc growth as they pertain to medical monitoring actions (i.e. working manuals, monitoring tips, and so forth.); • Involved in recruitment of potential Investigators, preparation of Independent Ethics Committee/ Independent Regulatory Board (IEC/IRB) submissions, notifications to regulatory authorities, translation of examine associated documentation, organisation of conferences and different duties as instructed by the PM; • Negotiates investigator budgets and assists with the execution of website contracts with assist from the authorized division; • Oversees all facets of examine website administration to make sure prime quality knowledge leading to constantly low question ranges and in good Quality Assurance stories; • Establishes, updates, tracks and maintains examine particular trial administration instruments/programs, and standing stories; • Communicates successfully with website personnel, together with the Principal Investigator (PI), and firm administration to relay protocol/examine 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 website • Experience of medical trial arrange processes • EDC working expertise • Full-time availabilityContact / to debate in additional element.#CRAjob

Tagged as: care, HR, IT, recruitment, research, science


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