Clinical Data Management Development Specialist, Remote, Europe
2 semanas atrás
.Clinical Data Management Development Specialist, Remote, Europe, LisbonClient:IQVIALocation:Lisbon, PortugalJob Category:Other-EU work permit required:YesJob Reference:ef7a8a305472Job Views:46Posted:23.01.2025Expiry Date:09.03.2025Job Description:Job DescriptionSummaryCollaborate with Subject Matter Experts and the Real World Evidence Data Management Team to develop and maintain Training Plan requirements and roles.Facilitate quarterly or annual training plan reviews.Develop training slides and material independently or with Subject Matter Experts.Plan, coordinate and communicate the training schedule for the Real World Evidence Data Management department.Perform training courses as needed and agreed with other stakeholders.Provide oversight of training delivered by other stakeholders.Monitor effectiveness and timeliness of training.Set up and maintain folder on Data Management SharePoint site.Update/archive training items in alignment with Training Plan updates.Plan and support development of Compliance Reports.Provide review and/or oversight of staff onboarding training compliance.Provide review and/or oversight of monthly/quarterly training compliance data.Collaborate with Managers to ensure adherence to training compliance targets.Participate, support or lead global initiatives to continuously improve training processes or compliance across Real World Evidence Data Management.Provide input on Data Management process improvements.Provide input on the development and implementation of a new technology or tool.Participate in focus teams, and global or local best practice teams as relevant.REQUIRED KNOWLEDGE, SKILLS AND ABILITIESSound working knowledge of clinical data management procedures, ICH-GCP, applicable regulatory requirements, medical terminology and quality management processes.Knowledge of Drug Development processes.Knowledge of CRO or Pharmaceutical Industry operations.Sound knowledge of current training practices.Good organizational, interpersonal and communication skills.Good judgement and decision-making skills.Strong influencing and negotiation skills.Strong computer skills including Microsoft Office and Data Management applications including EDC (Medidata Rave).Demonstrated ability to work in a matrix environment.Excellent problem-solving skills.Ability to travel within the region/country.Ability to lead and motivate a training team.Ability to establish and maintain effective working relationships with co-workers, managers and clients/customers.IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
Learn more at.Please note that if you are NOT a passport holder of the country for the vacancy you might need a work permit.
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Lisboa, Lisboa, Portugal TN Portugal Tempo inteiroClinical Data Management Development Specialist, Remote, Europe, LisbonClient:IQVIALocation:Lisbon, PortugalJob Category:Other-EU work permit required:YesJob Reference:ef7a8a305472Job Views:46Posted:23.01.2025Expiry Date:09.03.2025Job Description:Job DescriptionSummary1. Collaborate with Subject Matter Experts and the Real World Evidence Data Management Team...
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