Clinical Programmer FSP - based in South Africa

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special a deep conviction in what we do.

Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.

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 longterm 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 fastpaced 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 userfriendly.
• 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 TSQL 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 orClinical 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 setup 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 longterm 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 bestselling but equally we enable more niche drug developments that are critical to the wellbeing of many patients.

Youll be an influential member of the wider team.

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