Worldwide Clinical Trials jobs

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OFFICE ADMINISTRATOR - NOTTINGHAM - OFFICE BASED

Collaborate with internal teams and stakeholders to identify and define value-add analytics in The organisation of administrative services, including telephone, mail, courier and reception. Ensure incoming calls and correspondence...

CompanyWorldwide Clinical Trials
AddressNottingham, Nottinghamshire
CategoryAdministrative
SalaryCompetitive
Job typeFull Time
Date Posted 3 days ago See detail

Office Administrator - Nottingham - Office Based

Worldwide Clinical Trials

Nottingham, Nottinghamshire

Competitive

Collaborate with internal teams and stakeholders to identify and define value-add analytics in The organisation of administrative services, including telephone, mail, courier and reception. Ensure incoming calls and correspondence...

Associate Director, Clinical Data Management - Europe - Office or Home Based

Worldwide Clinical Trials

Nottingham, Nottinghamshire

Competitive

Lead and manage staff performing Data Management and Data management database development. Develop staff members, including the performance of staff appraisals and continued management. Contribute to the strategic management of th...

Senior Medical Writer - Europe - Home-based

Worldwide Clinical Trials

London, Greater London

Competitive

Dynamic global team with comprehensive peer, leadership and administrative support. Multi-levelled team, with ongoing training and opportunities for career development. Writing a wide range of documents across many therapeutic are...

Senior Clinical Research Associate (CRA) - UK - Home-based

Worldwide Clinical Trials

London, Greater London

Competitive

Conduct all types of visits - site qualifications, initiation, interim monitoring, site management and study close-out visits. Review study subject safety information and informed consent and conduct source document verification f...

Regulatory Compliance Quality Operations Manager - EMEA - Homebased

Worldwide Clinical Trials

London, Greater London

Competitive

Maintains knowledge in relation to GxP activities. Conduct regulatory intelligence/surveillance for GxP requirements globally. Identify quality impact and actions and advise on requirements for Worldwide systems, processes and tra...