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(R).
About the Role
We are seeking a Senior Clinical Data Engineer to join our team. As a Senior Clinical Data Engineer, you will drive the strategic design and implementation of data management solutions that enable efficient clinical trial operations and regulatory compliance. This position plays a critical role in managing data ingestion, quality assurance, and reporting infrastructure that supports study execution and patient safety. You'll collaborate with cross-functional teams including project managers, biostatisticians, and regulatory specialists to deliver first-time-quality data solutions.
You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through leading technical innovation, mentoring emerging talent, and establishing best practices in clinical data management. With diverse teams and continuous learning opportunities, the Senior Clinical Data Engineer can explore career paths and expand skills across clinical research, data engineering, and regulatory science.
Key Responsibilities
Lead the design, implementation, and management of Data Receipt Agreements with vendors and coordinate with cross-functional teams to establish efficient data transfer protocols
Program and establish import procedures for data ingestion using SAS, SQL, R, or alternative technologies such as Workbench, ensuring seamless integration of external data sources
Develop and execute comprehensive reconciliation checks and validation protocols to ensure accurate and complete data transfer across all systems
Design and program offline listings and custom reports that provide actionable insights to study teams and clients, enabling data-driven decision making
Aggregate and manage data across multiple sources, handling missing values, raw data files, data structures, and complex programming challenges with precision and accountability
Review and analyze data outputs to identify patterns, anomalies, and opportunities for improvement, providing strategic insights to enhance study quality and efficiency
Maintain accountability for first-time quality on all deliverables, ensuring compliance with SOPs, regulatory guidelines, and industry standards including ICH-GCP and 21 CFR Part 11
Lead and coordinate programming teams to successful project completion within established timelines and budgets, while monitoring resourcing and managing scope changes
Manage the deployment and optimization of data management technologies including SAS, Workbench, R, and other systems used for creating offline listings and data solutions
Develop, implement, and maintain technical documentation, data standards, and quality processes that ensure traceability, regulatory compliance, and operational efficiency
Mentor and provide technical guidance to team members and project teams, fostering a culture of continuous improvement and technical excellence
Participate in business development activities including bid defense meetings, contributing technical expertise to support new business opportunities
You'll thrive in this role if you bring:
Advanced technical proficiency in at least one programming language (SAS, SQL, or R) with demonstrated ability to design and implement complex data solutions
Strong leadership and mentoring capabilities with the ability to motivate and guide virtual teams across multiple time zones and cultures
Extensive experience working in clinical research or regulated environments with deep knowledge of clinical trial processes and data management best practices
Excellent communication and interpersonal skills with the ability to translate technical concepts for diverse stakeholders and build strong working relationships
Demonstrated commitment to first-time quality, methodical problem-solving, and continuous process improvement in complex technical environments
Comfort working with multiple data management systems and technologies, with the ability to quickly master new tools and adapt to evolving technical landscapes
Strong analytical and strategic thinking skills with the ability to identify opportunities for efficiency improvements and innovation in clinical trial operations
Required Qualifications:
Bachelor's degree in a relevant science discipline or equivalent work experience
Minimum 5+ years of experience in clinical research, data management, or a related field
Proficiency in at least one programming language (SAS, SQL, or R) with demonstrated expertise in data manipulation and analysis
Hands-on experience working with at least two clinical data management systems (such as SAS, Workbench, or Elluminate)
Strong knowledge of ICH-GCP, regulatory requirements, SOPs, system life cycle methodologies, and applicable regulations including 21 CFR Part 11
Demonstrated leadership experience mentoring team members and managing technical projects
Excellent written and oral communication skills in English with the ability to present complex technical information clearly to diverse audiences
Parexel is a clinical development services company that provides comprehensive solutions across clinical trials, regulatory affairs, consulting, and market access. The company is dedicated to improving global health by supporting the development of therapies that benefit patients worldwide. Parexel operates as a Contract Research Organization (CRO) serving the pharmaceutical and biotech industries, with expertise in GxP compliance, clinical research operations, and technology auditing. Every employee contributes to therapy development with a focus on empathy, quality, and making a meaningful difference in patient outcomes.
