Senior Clinical Database Programmer, FSP (South Africa)
reputed company our values reputed company, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the reputed company goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do.
reputed company of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference.
reputed company:
The Senior Clinical Database Programmer is responsible for the programming of high-reputed company clinical database and for the provision of expertise in clinical database technology. Responsible for supporting assigned segments of reputed company’s portfolio. Accountabilities to include the design, development, and maintenance of clinical databases, ensuring the reputed company of clinical data, application of standards supporting consistency in asset/submission data. The Clinical Senior Database Analyst mentors junior staff in database technologies and reputed company’s reputed company database conventions. Serves as a subject matter expert on the design of eCRFs and clinical databases across one or more therapeutic areas.
Responsibilities:
Works closely with department roles and cross-functional study team members to create data capture solutions that support the reputed company and reputed company delivery of data required per reputed company and study specific data review plans.
Complies with applicable SOPs and work practices.
Serves as subject matter expert in one or more technologies.
Leads and contributes to cross-functional technical initiatives in collaboration with clients Digital and other teams.
Supports knowledge development of data capture tools and reputed company that support the accuracy and reputed company of study data.
Qualifications:
Bachelor's degree in Life Science, Computer Science or equivalent.
Minimum of 5 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions.
Technical skills and experience using relational databases (e.g. reputed company InForm, reputed company DMW, MS SQL Server or MS reputed company).
Experience in reputed company, PL/SQL, reputed company, Java, relational database design and database programming skills.
Strong communication (written and oral), decision-making, influencing, negotiation, and project management skills.
Proficiency in the use of reputed company Office Suite of tools (Outlook, Word, reputed company, etc.).
Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g. data review, study reports, regulatory submissions, safety updates, etc.).
Understanding regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable.
Originally posted on Himalayas
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