[Hiring] Clinical Database Programmer II @Parexel

Role Description

We are seeking a Clinical Database Build Programmer II to join our team. As a Clinical Database Build Programmer II, you will support clinical research activities that advance new treatments for patients. This position plays a key role in database design, implementation, and quality assurance across clinical data management systems. You'll collaborate with cross-functional teams, follow industry-standard processes, and contribute to study operations from planning through closeout.

• Create, implement, and execute procedures to build and maintain database set-up for paper-based and web-based (EDC) clinical data management systems in standard or CDISC-compliant format as required, including annotation of case report forms where applicable.
• Create, implement, and maintain consistency checks in standard or CDISC format for database builds, following internal and external regulatory requirements.
• Deliver first-time quality on all database-related deliverables and maintain accountability for accuracy and compliance.
• Provide technical feedback to study programmers on the creation of electronic case report forms following standard operating procedures and internal process guidelines.
• Assist in providing technical solutions to internal and external client inquiries related to database design and implementation.
• Develop and expand knowledge of clinical data management systems, electronic data capture, clinical trial management systems, safety reporting, and programming languages used within the organization.
• Maintain all supporting documentation for studies in accordance with standard operating procedures and guidelines to ensure traceability and regulatory compliance.
• Maintain technical documentation applicable to clinical databases and document any deviations for dissemination to project teams.
• Participate in the creation of standards through tools, libraries, or processes to ensure efficient and effective database management practices.

Qualifications

• Strong attention to detail and commitment to quality in a regulated environment.
• Excellent written and oral communication skills in English.
• Ability to learn new systems and function effectively in an evolving technical environment.
• Ability to collaborate across teams, including international teams, as well as work independently.
• Strong organizational skills, ability to manage competing priorities, and flexibility to adapt to change.
• Customer focus, commitment to quality management, and strong problem-solving abilities.

Requirements

• Bachelor's degree in relevant science discipline or equivalent work experience.
• At least 3 years of experience in clinical data management or database programming.
• Experience in at least one programming environment (e.g., SAS, CDMS, EDC, SQL, VB, Java).
• Knowledge of standard operating procedures, guidelines, and system life cycle methodologies.
• Knowledge of ICH-GCP and applicable local and international regulations such as 21 CFR Part 11.
• Strong communication, organization, and problem-solving skills.

Preferred Qualifications

• Experience with electronic data capture (EDC) systems.
• Familiarity with CDISC standards and CDMS platforms.
• Experience in a clinical research or healthcare environment.

Benefits

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.