Senior Clinical Database Programmer

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Skills you'll use

What you'll do

• 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.

Who can apply

• 6 to 7 years of experience in clinical data programming
• Proficiency in at least one programming environment (e.g., SAS, CDMS, EDC, SQL, VB, Java)
• Strong knowledge of SOPs, guidelines, work instructions, SDLC methodologies, ICH-GCP, and applicable regulatory requirements including 21 CFR Part 11
• Demonstrated experience in the clinical research industry or similar regulated environment
• Strong communication, organization, and problem-solving skills with proven ability to work independently and collaboratively

About Parexel

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