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.
Job Responsibilities:
Create and maintain standardized data visualizations to support Medical Data Review and safety signal detection, following established templates and guidance.
Apply defined visualization standards to generate outputs aligned with Risk-Based Quality Management (RBQM) principles and Critical to Quality (CtQ) endpoints.
Work under guidance to implement visual analytics within timelines tied to First Patient In (FPI) or predefined safety milestones.
Support documentation and quality control of visualization deliverables to ensure traceability and compliance.
Participate in training sessions and incorporate feedback from more experienced Real-time Visual Analytics Specialists.
Assist in responding to basic stakeholder requests and clarifying data availability or visualization functionality.
Work under general supervision and apply independent judgment to interpret guidance, prioritize responsibilities, and make decisions in situations that require contextual understanding.
Apply judgment to address moderately complex statistical or data issues, balancing scientific rigor with appropriate flexibility, and seek guidance when facing novel or ambiguous situations.
Adhere to functional standards by participating in peer review and mentoring relationships to uphold quality and build methodological and regulatory expertise.
Here are a few requirements specific to this advertised role.
Bachelor’s degree in life sciences, computer science, data science, bioinformatics, or a related field.
2 years+ experience in clinical data, visualization, or analytics.
Familiar with Spotfire visualization tools.
A basic understanding of clinical trial data and common data structures (e.g., CRF data).
Demonstrate a strong attention to detail, logical thinking, and an eagerness to learn visualization standards and clinical workflows.
Able to communicate effectively in English, both in writing and verbally.
The following would also be advantageous:
Exposure to clinical or safety data structures and terminology (e.g., adverse events, lab results, dosing).
Familiarity with Risk-Based Quality Management (RBQM) concepts and their role in early development.
Experience with interactive tools such as Tableau, Power BI, R/Shiny or Python.
Ability to follow visual design templates and apply style consistency.
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 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.
