Clinical Programmer I Task Headquarters
3 months ago
**Overall Purpose of the Position**:
While projects may vary, your typical responsibilities might include collaborating and communicating with a variety of colleagues and customers to develop and setup Clinical Database Management System (CDMS) and Laboratory Information Management Systems (LIMS) for Clinical Studies; to provide technical support in the review and development of annotated eCRFs and programming database edit specifications and to support the Data Management team with the development and production of data manual review listings. Other responsibilities include the programming of Data Reconciliations and SDTM Sponsor/Statistician Listings.
Join our growing Data Management team and discover your extraordinary potential You will enjoy a varied role working for different sponsors across several therapeutic areas within phases I-IV. The position offers a strong support network, flexible working solutions, and the opportunity to progress your career.
If you are detail focused, with a real understanding of the importance of quality in everything related to your role at TASK and looking to strengthen your expertise within a varied and dynamic environment, then this is a fantastic opportunity.
**Key Performance Areas (KPAs) & Responsibilities include, but not limited to**:
- Annotation of eCRFs
- Setup and Programming of Clinical Database Management Systems (CDMS).
- Annotation of Lab Trial Plans.
- Setup and Programming of Laboratory Information Management Systems (LIMS).
- Programming of Database Edit Specifications
- Review of Data Transfer Agreements (DTA) or Specifications (DTS).
- Programming of Data Reconciliations and Manual Review Listings
- Programming of SDTM Sponsor/Statistician Listings
- Producing Define XML / PDFs, Analysis Results Metadata (ARM), and Reviewers Guides to support SDTMs.
**Ideal Requirements**
- Minimum of Diploma or Bachelors or Masters’ in Computer Science, Mathematics, Engineering or equivalent
- Experience in SQL Programming in Database Programming
- Excellent knowledge of CDISC standards (SDTM)
- Knowledge and Experience with Clinical Trial Data
- Knowledge of ICH-GCP with a strong interest in clinical research
- Professional use of the English language; both written and verbal
- High ethics and good programming practice skills
- Advanced computer skills
**Key Personal Inherent Characteristics**
- Delivering high performance and an excellent communicator who listens effectively and accurately and clearly conveys information through verbal and written means
- Driving quality by displaying ability to clarify and reduce complex issues to simple solutions
- Ability to anticipate problems and resolve problems before they occur
- Recognize recurring issues and analyse their causes in order to reach a solution
- Excellent planning & organising skills with the ability to work systematically and sequentially
- Personal effectiveness and the ability to work in a pressurised environment
- Maintain good relationships with colleagues and customers
- The ability to adapt working hours, key outcomes, and competencies in response to the business needs which may change from time to time in response to strategies and operational requirements
**Details**:
**Area**:Parow, Cape Town
**Contract Type**: Permanent
**Applications Close**: 23 October 2024
TASK reserves the right to withdraw this advertisement and not fill the above-mentioned vacancy at any stage during the recruitment process.
Meeting our employment equity goals will be acknowledged during the recruitment process
**Job Types**: Full-time, Permanent
Application Question(s):
- What is your notice period?
- What are your gross salary expectations?
- Do you possess the necessary Qualification?
Application Deadline: 2024/10/23
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