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Study Clinical Programmer

This job is no longer available

Employer
Key People Pharmaceutical
Posted
Friday, June 22, 2012
Closes
Friday, July 20, 2012
Ref
1203-45
Contact
Tim Barratt
Location
South East England, England
Job Role
Contract Type
Permanent
Hours
Salary
GBP35000 - GBP40000 per annum

Further information


Main responsibilities:
*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

Experience Required:
You're someone who wants to influence your own development. You're looking for a company where you have the opportunity to pursue your interests across functions and geographies, and where a job title is not considered the final definition of who you are, but the starting point.
You will be educated to a degree level or equivalent in a scientific or relevant technical degree and experience with handling biomedical data and relational databases.
As clinical Programmer you will show significant working experience with a programming language 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, transformation or reporting
You will 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.

To be considered for this position, please apply using the link below and when completing your application, please ensure you attach an up to date CV and details of your current remuneration package.

Key People Pharmaceutical


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