Veeva Jobs in England

5 Veeva Jobs in England

Research Nurse, Clinical trials, Leeds

Leeds, West Yorkshire, United Kingdom
Confidential
ILS certification to be gained in role. A plus, but not a must, if you bring previous experience with Electronic Data Capture tools and Veeva Previous Research Nurse experience is ideal, but not a must. We are open to consider recent graduates or any recent nursing experience. The important more »
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Quality System Management

London Area, United Kingdom
BioTalent
to join the team on a hybrid, contract basis. The Role: Support the maintenance of the Quality Management System, act as Business Administrator for Veeva eQMS, oversee quality associated records and ensure these activities conform to regulatory requirements. Manage the controlled document scheme, act as GxP archivist, and deliver … QA training activities. duties within Quality function. It is desirable, but not essential for the candidate to have a comprehension of basic Veeva configuration to assist them with troubleshooting issues that my arise and to complete basic configuration changes such as workflow adjustments and additions and removals to configured … lists Profile Required Essential: Act as Business Administrator for Veeva QualityDocs, Veeva eQMS and Veeva training. Act as the core subject matter expert for the company document management system, be the primary point of contact for document management queries and represent the system during regulatory and client more »
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Associate Director

London Area, United Kingdom
RBW Consulting
written and verbal communication abilities. Insightful understanding of end-user needs. Experience in brand strategy development and implementation. Familiarity with CRM platforms such as Veeva and Salesforce Marketing Cloud. Competence in patient and healthcare professional journey planning. What's on Offer: This agency values work-life balance and offers more »
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Quality Assurance Associate

Liverpool, England, United Kingdom
SRG
Experience of working in a cGMP environment – QC/QA Experience of Quality Assurance systems, procedures and industry practices is desirable (e.g. SAP, trackwise, Veeva more »
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Manager, Submission Management, Clinical Trials

Central London, London, United Kingdom
Bristol-Myers Squibb Co
compliance with study timelines, BMS SOPs, worldwide regulatory guidelines and regulations. Comply with the use and maintenance of the available planning & tracking tools (e.g. Veeva - HA submission and approval Tracking system) to generate reports and track the CTA content and associated dates. Escalate to study teams and GSM-CT more »
Employment Type: Permanent
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