Clinical Database Jobs in Maidenhead

SRG - Maidenhead, United Kingdom

SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office...

from: uk.lifeworq.com - 2 days ago

Consult - Maidenhead SL6, Berkshire, South East

Ensure timely achievement of study deliverables in accordance with global regulatory strategies and evolving global clinical trial legislation, including compliance with the EU Clinical Trial Regulation...

from: joblookup.com (+1 source) - 22 days ago

SRG - Maidenhead, Berkshire, United Kingdom

SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office... £22 - £35.00/hour

from: CV-library.co.uk - 24 days ago

SRG - Maidenhead, Berkshire, United Kingdom

Excellent understanding of the legislation governing the conduct of global clinical trials and evolving regulatory environment, Good Manufacturing Practices and Good Clinical Practices, ICH and other pertinent... £65 - £75/hour

from: CV-library.co.uk - 24 days ago

Consult - Maidenhead, United Kingdom

Ensure timely achievement of study deliverables in accordance with global regulatory strategies and evolving global clinical trial legislation, including compliance with the EU Clinical Trial Regulation...

from: uk.lifeworq.com - 14 days ago

Regeneron - Uxbridge, England, United Kingdom

Supervising team for the initiation and approval of the building, and validation of clinical databases, subsequent changes in clinical databases and data validation activities. Coordinates with clinical...

from: jobleads.co.uk (+1 source) - Yesterday

reading, england, United Kingdom

Manage Clinical Research Organization (CRO) interactions, including sponsor oversight of relevant functional activities (e.g., study management, monitoring, site management, project master files, and data...

from: jobleads.co.uk - 7 days ago

UNIVERSITY OF SURREY - Guildford, Surrey, England

The Senior Study Coordinator will be responsible for the set-up and day-to-day conduct of studies undertaken in the CRF, ensuring the accurate collection and reporting of study data, and the safety and... £36,024 to £44,263 per annum

from: timeshighereducation.com - 4 days ago

reading, england, United Kingdom

The HE&Epi team works in a range of disease areas. In addition to observation studies using a variety of study designs, including prospective and retrospective data collection, analysis of clinical and...

from: jobleads.co.uk - 2 days ago

Regeneron - Uxbridge, Middlesex, United Kingdom

Oversees setting up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS) and Trial Master File (TMF) Contributes to investigator meeting preparation and... Competitive

from: pharmiweb.jobs - 13 days ago