Clinical Programmer (FSP) - based in South Africa

Welcome to the Latest Job Vacancies Site 2025 and at this time we would like to inform you of the Latest Job Vacancies from the Parexel with the position of Clinical Programmer (FSP) - based in South Africa - Parexel which was opened this.

If this job matches your qualifications, please send your application directly through our latest Job site. Indeed, every job is not easy to apply because it must meet several qualifications and requirements that we must meet in accordance with the standard criteria of the Company who are looking for potential candidates to work. Good job information Clinical Programmer (FSP) - based in South Africa - Parexel below matches your qualifications. Good Luck: D

Parexel is currently seeking a Clinical Programmer to join us in South Africa, dedicated to a single sponsor.

This role will be responsible for the provision of data review and trial management deliverables across all compounds and trials for which these are required, and for all functional groups that require those deliverables.

Working as a Clinical Programmer at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.

Expect exciting professional challenges in inspiring studies, but with time for your outside life.

Responsibilities

• Program simple to complex data review listings, exception reports, QTL/KRIs, metrics reports and visualizations in a fast-paced environment for clinical trial data review and management purposes.
• Liaise with Clinical Data Management and/or cross functional staff to understand the needs of the end users of the listings, reports, and metrics.
• Contribute to the development of software systems and related infrastructure to generate displays of clinical study data and metrics reports that are efficient and user-friendly.
• Create and document archives of software and deliverables.
• Create any Work Instructions process and training documents needed related to clinical programming and the required deliverables.
• Provide time and resource estimates for project planning as well as accurately record time spent on multiple deliverables.

Here are a few requirements specific to this advertised role.

• Bachelors degree in computer science, Statistics, Mathematics, Life Sciences or other relevant scientific fields.
• Minimum of 5 years of experience in developing software in a clinical trial environment using SQL, including at least 3 years of clinical programming experience.
• Skilled in programming in a relational database setting with SQL and/or T-SQL or ETL.
• Experience with data reporting tools in a clinical trial setting.
• Experience in the Biotechnology, Pharmaceutical, or Life Sciences industries (Clinical Research Organization - CRO or Clinical Trial regulated environment preferred).
• Experience with the eClinical Solutions elluminate platform a plus; experience with Qlik Sense a plus.
• Preferred additional external data transfer experience in:

• Creating external data transfer specifications, ensuring external clinical trial data are compatible with the clinical database to support data integration, analysis and reporting.
• Experience in planning, set-up, and acquisition of external clinical data at the study level
• Liaising with and reviewing work delivered by external partners (e.g. laboratories, eCOA providers, technology providers, etc.)

• Knowledge of some additional programming languages (e.g.: SAS, PL/SQL, R, Python, Java, …) a plus.
• Ability to balance and prioritize multiple assignments and respond quickly to ad hoc requests.
• Familiarity with CDISC standards, including CDASH and SDTM.
• Working knowledge of Microsoft products: Outlook, Word, Excel, Teams.
• Excellent verbal and written communication skills.
• Strong English language written and verbal communication skills.

We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of todays top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

Youll be an influential member of the wider team.

Not quite the role for you?

Join Our Talent Community and well reach out with job alerts when positions that match your career interests become available. Well also share periodic updates about the latest company news and events.

Sign up today https://jobs.parexel.com/functional-service-provider

Information :

• Company : Parexel
• Position : Clinical Programmer (FSP) - based in South Africa
• Location : Pretoria, Gauteng
• Country : ZA

How to Submit an Application:

After reading and knowing the criteria and minimum requirements for qualifications that have been explained from the Clinical Programmer (FSP) - based in South Africa job info - Parexel Pretoria, Gauteng above, thus jobseekers who feel they have not met the requirements including education, age, etc. and really feel interested in the latest job vacancies Clinical Programmer (FSP) - based in South Africa job info - Parexel Pretoria, Gauteng in 2025-02-28 above, should as soon as possible complete and compile a job application file such as a job application letter, CV or curriculum vitae, FC diploma and transcripts and other supplements as described above, in order to register and take part in the admission selection for new employees in the company referred to, sent via the Next Page link below.