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Online Resumes with "Clinical study Associate"
Lead clinical study associate with extensive experience in delivering clinical study support to internal and external research partners. Track record of ensuring adherence to study timeline and budget parameters and compliance with regulatory agencies, study protocol, and corporate / sponsor requirements. Demonstrated success implementing process improvements to reduce site initiation time and improve internal and study sit...
Tags for this Online Resume: Project Materials Preparation / Review, Team Supervision & Training, Workload Planning, Document Management / Auditing, Timeline / Budget Management, Clinical Supply Inventory Maintenance
Office support professional experienced in fast-paced environments demanding strong organizational skills, technical and interpersonal skills. Trustworthy, ethical, and discreet, committed to superior customer service. Confident and poised interactions with individuals at all levels.
Professional Summary A certified professional Clinical Research with 4 years of experience in Clinical Research coordination and a year experience as Clinical Study Associate. Expertise in QC of documents, remote Monitoring and supporting the management by handling the tasks of multiple clinical research studies managing eTMF's & designing Clinical Portfolio's from Sponsor end. Expert in liaising between different departmen...
Tags for this Online Resume: Document Management, Monitoring - Remote and onsite, Clinical Research coordinator, Device trials, clinical Research, Project Management, QC and QA, Pharmacovigilance, Ethics and compliance, regulatory, Clinical study Associate, Multiple therapeutic areas experience, Phase 1-4 trials, Audits and Inspection readiness, Multiple software and application experience - Veeva VAULT , Impact , Quest , Sentinel,Tesla, EDC experience- RAVE Medidata, IRT system experience Clinpace , Endpoint