Dear AllStat,
CK Clinical is recruiting for a Clinical Data Manager with CDISC
Experience to join an International CRO at their site based in Brussels on a contract basis.
As
Clinical Data Manager, you will have the following responsibilities:
·
Content and structure analysis of the legacy data and the clinical trial protocol
·
Annotation of Case Report Forms using CDISC Terminology
·
Preparation of clinical data CDISC conversion definitions
·
Development of project documentations (Data Reviewers Guide and Data Handling Report)
·
Validation of the data and metadata according to the applicable CDISC standards and guidelines
·
Quality Control of all project deliverables
·
Responsibility for the timely delivery of a CDISC-compliant submission package
·
Contribution to the definition of CDISC validation checks
As Clinical Data Manager, you will have the following qualifications,
skills and experience:
·
Master's degree in scientific or healthcare discipline or equivalent through experience
·
Experience in a clinical trial environment
·
Strong understanding of data management and database administration: clinical protocol assessment, Case Report Form design, understanding of clinical data management
systems, study start up (database administration, edit check creation/validation) and data base lock.
·
CDISC knowledge is a plus
·
Good knowledge of ICH/GCP
·
Basic SAS knowledge
·
Good English written and oral communication skills
·
Quick learner
·
Excellent team player
·
Able to plan work in order to meet deadlines
For more information or to apply for this Clinical Data Manager position, please contact Mylene Paumier on
+44 (0)207 470 5672 or email:
[log in to unmask]" target="_blank">[log in to unmask].
Best regards,
Mylene
Mylene Paumier
Consultant
CK Clinical Limited
Crown House
72, Hammersmith Road
London
W14 8TH
DD: +44 (0)207 470 5672
Tel: +44 (0)207 470 5670
CK Clinical, CK IT, CK Regulatory and CK Science are trade names of CK Associates Limited
Registered in England No 2611749
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