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Study Data Manager
Eingestellt von Chiltern
Projektbeschreibung
•11 month maternity contract role for Study Data Manager
•Office based role with global pharma based in Hertfordshire
•Role would suit a Freelancer
•Study Data Manager must have hands on experience of working in early phase data management
Job Background
The Resourcing Solutions (RS) department of Chiltern acts in a similar way to that of a staffing solutions provider. The department is currently seeking a contract Study Data Manager to work for a global Pharmaceutical company in Hertfordshire. Working across a number of studies, candidates must have a minimum of two years hands on experience in early phase data management. This experience must be within their current position. Working across a number of therapeutic areas, with global study teams across the UK.
Job Primary Functions
The Study Data Manager (SDM) represents all Clinical Data and Information Sciences (CDIS) functions (including timely database set-up, collection, processing and correction of clinical trials data) and is responsible and accountable for the leadership, planning and delivery of CDIS activities of one or more study(ies) to be completed with high-quality and on time. The SDM is a core member of the Study Management Team (SMT).
Models adopted include Insourced studies which are fully managed internally but with some activities performed remotely, and Outsourced studies which are managed by a CRO and the Study Data Manager maintains sponsor oversight.
Job Qualifications
•College/University degree in life sciences or related subject,
•Proven knowledge and experience of using computer applications.
•Excellent written and verbal English communication skills demonstrated by ability to present clear instruction/direction to individuals and teams.
•Experience of working as part of or leading a team with a proven ability to make an active contribution to the team's performance.
•Self-motivated, and takes initiative, for example, manages issue resolution to conclusion without the need for continual supervision.
•Proven organization skills demonstrated by the ability to understand instructions and deliver against commitment on time.
•Knowledge of relational databases and experience using clinical data management systems and tools.
•Experience of project managing the data management activities of a clinical study.
•Desired but not essential - experience in early phase clinical development.
•Caniddates must have the leagl authorisation to work in the UK
MORE INFORMATION AVAILABLE ON REQUEST
For a confidential discussion about this opportunity, please phone Peter Lewis on (0) . To apply, please send your CV to
For more information about Chiltern, please visit our web site at
Keywords:
EDC, Electronic Data Capture, inform, Data Manager, DM, Lead Data Manager, Study Data Manager, pharma, pharmaceutical, CDM, Data Manager, DM, discrepancy management, Lead CDM, Lead Clinical Data Manager, Clinical data project Leader, Hertfordshire, London, UK, England
Projektdetails
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Einsatzort:
Hertfordshire, Vereinigtes Königreich
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Sonstiges