Dear ALLSTAT,

 

Jessica Todd is recruiting for a CLINICAL PROGRAMMER to work with a specialist technical team for a Global Pharmaceutical company based at their extensive site in the South East on a permanent basis.

 

As Clinical Programmer you will be involved in supporting global data handling activities by providing study databases and reporting tools for clinical data review, and the transformation of study data for analysis across a range of therapeutic areas.

 

The main responsibilities of the Clinical Programmer include:

 

•Creation and maintenance of clinical trial databases and related objects for the collection of patient data for clinical trials.

•Program derivations and conditions to control access to forms and fields.

•Review of data quality check specifications and programming data quality checks during the course of clinical studies.

•Development of programs for extracting and transforming patient data into the appropriate data model to support reporting and analysis activities.

•Customizes standard report templates to produce study-specific reports for data cleaning and Medical Data Review.

•Supports study closeout activities.

•Adherence to global standards and project related standards.

•Co-operate with local and international study teams to achieve efficient solutions.

•Contributes to the timelines for programming deliverables at the study level.

•Responsible for deliverables for one or more studies.

•Manages the handover and provides support to service providers on study-level tasks.

•Reviews and monitors study-level tasks performed by the service provider as needed.

•Provides technical mentoring.

•Effectively coordinates workload and communicates status of work.

 

 

As a Clinical Programmer,  the following qualifications, skills and experience are required:

 

- Educated to a degree level or equivalent in a scientific or relevant technical degree and experience with handling biomedical data and relational databases.

 

-Show significant working experience with one or more programming languages like SQL, PL/SQL, C# or SAS and/ or significant experience in one or more areas in Clinical Data Management clinical study database setup, edit check programming, data extraction, CDISC SDTM transformation or reporting.

 

-Have strong planning and organizational skills and the ability to manage multiple priorities, tasks or goals, developing and committing to realistic estimates and plans to complete required tasks or goals, developing and committing to realistic estimates and plans to complete required tasks.

 

You shall be working in a Global environment with interaction at all levels, so excellent communication skills are essential.

 

For more information, please contact me on 01438 842976 or via email [log in to unmask] with an updated CV for a quick response.

 

 

 

Kind regards,

 

Jessica Todd BA

Consultant - Biometrics

CK Clinical Limited

9 High Street

Stevenage

SG1 3BG

DD: 01438 842976

T: 01438 743047

F: 01438 723800

W: www.ckclinical.co.uk / www.ckmedics.com

 

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