Intern – Clinical Data Engineer

Reposted Yesterday
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Bloemfontein, Mangaung, Free State, ZAF
In-Office
Internship
Pharmaceutical
The Role
Paid 12-month internship supporting clinical data engineering activities, including SAS dataset programming, offline listings, custom reports, trend analysis, data review, third-party data ingestion and reconciliation. The intern will handle missing values, create data structures, manage programming errors, maintain study documentation, support quality and regulatory compliance, and collaborate with global teams under close supervision.
Summary Generated by Built In

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.

Your career starts here!


We are looking for ambitious recent graduates who are ready to take their first step into the professional world. This paid 12-month internship is designed to provide meaningful experience, structured learning, mentorship, and exposure to real projects that will help you grow both personally and professionally.


This is an opportunity for an Clinical Data Engineer internship.  The Intern Clinical Data Engineer works with close supervision to support various activities related to electronic data, and/or the application of computer and communication technologies. General areas of responsibility include programming offline listings, trend analysis, data review, ingestion, and reconciliation of third party data. All tasks should be performed in accordance with corporate quality standards, SOPs/Work Instructions/Guidelines, ICH-GCP and/or other international regulatory requirements.


General areas of responsibility also include:


  • Programming of offline listings and custom reports to allow better insights to all external data.
  • Handling Missing Values, reading raw data files, creating data structures, handling programming errors, accessing, and managing data, appending, and concatenating SAS datasets.
  • Accountable for first time quality on all deliverables.  
  • Maintain all supporting documentation for studies in accordance with SOPs/Guidelines/Work Instructions to ensure traceability and regulatory compliance. This includes the documentation of any deviations and dissemination of these to the rest of the project teams.
  • Work with global teams.

Requirements:


  • Final Year (Under-Grad Degree) or Honor Degree students in Information Technology, Computer Science, Data Science.

Please note - this Internship starts January 2027 and is office based in Bloemfontein


Closing Date: 30 October 2026

Skills Required

  • Final-year undergraduate student or Honor Degree student

Parexel Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Parexel and has not been reviewed or approved by Parexel.

  • Healthcare Strength — Health coverage is described as comprehensive, including medical, dental, vision, HSA/FSA options, and company-paid disability insurance. Descriptions often portray the package as strong or “top notch,” adding meaningful value.
  • Retirement Support — Retirement offerings include a 401(k) with company matching and, in some regions, generous pension contributions. Core financial protections are emphasized as a solid part of the total rewards.
  • Leave & Time Off Breadth — Time-off programs include ample PTO or flexible/unlimited RTO alongside flexible schedules and remote/hybrid options. Work-life balance support from managers is highlighted as a practical advantage.

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The Company
HQ: Raleigh, NC
20,524 Employees

What We Do

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

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