Senior Clinical Database Programmer

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

Join our team as a Senior Clinical Database Programmer on a 6-month contractual assignment . In this role, you will be responsible for supporting clinical database programming and ensuring high-quality data delivery for clinical studies.

As a Senior Clinical Database Programmer, you will provide technical expertise and strategic leadership in the design, implementation, and management of electronic data capture (EDC) systems and clinical databases that directly impact the integrity and success of clinical trials. This position plays a key role in ensuring regulatory compliance, data accuracy, and system optimization while advancing patient safety and research quality. You'll collaborate with cross-functional teams including sponsors, data management leaders, and clinical operations, follow industry-standard processes and regulatory requirements, and contribute to study operations from planning through closeout.

Responsibilities include leading EDC system setup and maintenance, designing and implementing consistency checks, mentoring programming teams, and supporting business development initiatives. With diverse teams and continuous learning opportunities, the Senior Clinical Database Programmer can explore career paths and expand skills across clinical research, positioning yourself as a trusted technical authority in clinical data management.

Key Responsibilities:
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Lead and supervise the design, implementation, and maintenance of electronic data capture (EDC) and clinical database management systems (CDMS) in standard or CDISC-compliant formats, ensuring regulatory compliance and first-time quality on all deliverables

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Create, implement, and maintain consistency checks and edit checks in standard or CDISC format, following internal SOPs and external regulatory requirements including 21 CFR Part 11 and ICH-GCP guidelines

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Provide technical leadership and mentorship to programming teams and project staff, including training on eCRF design, database procedures, and best practices in clinical data management

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Serve as the primary technical contact and liaison with sponsors, data management leaders, and cross-functional teams regarding database programming issues, technical solutions, and project timelines

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Manage database lock/unlock procedures and approve database changes in accordance with SOPs, ensuring adherence to service level agreements and regulatory requirements

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Maintain comprehensive technical and regulatory documentation for clinical databases, including deviation logs and traceability records to ensure compliance and audit readiness

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Support the integration and program