Clinical Research Associate

QUALIFICATIONS Job Description: Clinical Research Associate ( CRA) will be responsible for conducting clinical studies, managing & monitoring of study sites in accordance with SOPs, ICH-GCP

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DEneme

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Clinical Research Coordinator / Saha Görevlisi

JOB DESCRIPTION Site Coordinator_Job Description- Investigational site file management according to applicable SOPs,- High level of communication with site staff, study subjects and study CRAs

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Clinical Research Associate – sponsor dedicated

Clinical Research Associate (CRA).Oversee site monitoring responsibilities with remote and in-person visitsWork in a flexible environment with a close-knit teamUse time management and people skills

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Clinical Operations Manager (PLM)

counsel, guidance and support where necessary. Basic understanding of employment legislation or general people management. Desirable Criteria Previous experience as a Lead CRA or CRA Line Manager

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Senior Clinical Research Associate

to ensure ensuring compliance to the study protocol, Standard Operating Procedures, applicable regulations, and the principles of ICH-GCP. The CRA will also be charged with ensuring the quality and integrity

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CRA II – Senior CRA – Clinical Operations

Clinical Research Associate (CRA).Oversee site monitoring responsibilities with remote and in-person visitsWork in a flexible environment with a close-knit teamUse time management and people skills

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Clinical Trials Assistant

may also assist with general administrative functions as required.RESPONSIBILITIESAssist Clinical Leads, Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) with accurately updating

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Senior CRA (Home Based)

Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose

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