Senior Software Engineer
Parexel
Senior Software Engineer
Parexel
End-to-end clinical trials and regulatory consulting
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.
About Parexel
Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.
We work with focus, agility, and shared purpose: moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart®.
About the Role
We are seeking a Senior Software Engineer to join our team, supporting the clinical research and pharmaceutical industries. As a Senior Software Engineer, you will design, implement, and architect software products and product extensions that support clinical trial information sharing and the pharmaceutical clients we serve. This position plays a key role in delivering the software and data solutions that clinical research depends on, supporting data quality, efficient information sharing, and reliable application support.
You'll collaborate with stakeholders across matrix teams, follow agreed development standards and Agile practices, and contribute from design through live deployment. Responsibilities include designing and architecting software and database solutions, mentoring Software Engineers, producing technical artifacts, and supporting release management, with opportunities to deepen your expertise and shape solutions that influence clinical programs.
You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through designing clinical trial information sharing solutions, delivering technical consulting to pharmaceutical clients, and mentoring fellow engineers. With diverse teams and continuous learning opportunities, the Senior Software Engineer can explore career paths and expand skills across clinical research.
Key Responsibilities
You'll thrive in this role if you bring:
Required Qualifications
We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.
If this job doesn't sound like the next step in your career, but perhaps you know of someone who'd be perfect fit, send them the link to apply!
Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.
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