Skip Navigation

Jobs at Parexel

We know just how important it is to put people first. It's with that human touch that we've played a part in nearly all of the top 50 treatments on the market. And every day, we're focused on working with industry leaders to bring life-changing healthcare to patients across the globe. Whether you join our Clinical, Consulting, Biotech, Functional Service Provider (FSP), or other teams, we're doing it With Heart ™.

Clinical Database Programmer II

Job ID R0000002125 South Africa, Remote

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's 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 we're committed to making a difference.

The Clinical Database Programmer II provides technical expertise for the conduct of clinical trials and works with minimal supervision to support various programming activities related to clinical systems, and/or the applications/systems within eClinical technologies.

General areas of responsibility also includes: eCRF design, edit check programming, edit check validation and integration of third-party systems with the EDC databases. All tasks should be performed in accordance to corporate quality standards, SOPs/Work Instructions/Guidelines, ICH-GCP and/or other international regulatory requirements.

Ideal candidate will possess:

  • Written and oral fluency in English.

  • Experience in at least one programming environment (e.g. SAS, CDMS, EDC, SQL, VB, Java).

  • Knowledge of SOPs/Guidelines/Work Instructions/System Life Cycle methodologies, ICHGCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.

  • Experience working with at least one system used within the Clinical Trial process (e.g. SAS, CDMS, EDC (Inform, RAVE, DataLabs, Medrio, Veeva), CTMS, Medical Safety Reporting).

  • Experience in clinical research industry or similar field is desired.

  • Bachelor’s degree (or equivalent) in a relevant science discipline.

  • Strong ability to collaborate with global teams and work independently.

  • Strong interpersonal, oral and written communication skills using concise phrasing tailored for the audience with a diplomatic approach.

  • Demonstrate ability to learn new systems and function in an evolving technical environment.

  • A flexible attitude with respect to work assignments and new learning; ability to adjust rapidly to changing environments.

  • Customer focus to interact professionally and respectfully within Parexel and all external colleagues to build rapport and trust.

  • Basic presentation skills.

  • Time management and prioritization skills in order to meet objectives and timelines.

  • Proven problem-solving skills including capability to make appropriate decisions in ambiguous situations, ability to conduct root cause analyses.


#LI-REMOTE

Join our Talent Community

Welcome to the Parexel Talent Community! Sign up below and we’ll reach out with job alerts when positions that match your career interests become available. We’ll also share periodic updates about the latest company news and events.

Recently Viewed Jobs

You have not recently viewed any jobs

View all jobs

RECRUITMENT FRAUD ALERT

It has been brought to our attention that there has been fraudulent activity by scammers attempting to represent themselves as Parexel employees or recruiters. These individuals are attempting to reach potential job seekers through online chat interviews and sending false offer letters, representing Parexel without our consent. If you’re concerned that you’ve been contacted by an unauthorized Parexel recruiter or employee, please notify Jobs@Parexel.com. You may also report suspicious fraudulent activity to your local law enforcement agency or the FBI. Thank you.

@* *@