Clinical Study Builder in Canada Creek, Nova Scotia at Jobgether

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Clinical Study Builder in Canada.

As a Clinical Study Builder, you will play a pivotal role in designing, developing, and configuring electronic case report forms (eCRFs) and associated study components for clinical research. Working in a collaborative, fast-paced environment, you will ensure study data integrity while supporting seamless integration with statistical and data management teams. Your work will directly impact the efficiency and quality of clinical trials, providing critical support for research teams and contributing to the advancement of medical knowledge. This role offers exposure to leading clinical data management systems, cross-functional collaboration, and opportunities to influence study design and execution. You will combine technical expertise with attention to detail, ensuring regulatory compliance and high-quality outputs.

• Develop, configure, and maintain eCRFs, visit schedules, edit checks, derivations, integrations, migrations, and reports using systems such as Veeva CDMS, Medrio, and Rave.
• Lead design and review meetings for study protocols, ensuring alignment with regulatory and project requirements.
• Provide technical and user support to internal and external stakeholders, troubleshooting and resolving issues efficiently.
• Conduct end-user training and maintain documentation, including updates to Standard Operating Procedures (SOPs).
• Collaborate closely with Lead Data Managers and vendor partners throughout testing, deployment, and post-release changes.
• Manage multiple study builds or updates simultaneously, maintaining accuracy and adherence to timelines.

• Bachelor’s or Master’s degree in a relevant field.
• Minimum of 2 years of experience in Veeva CDMS study builds; experience with Medidata Rave preferred.
• Certification as a Veeva Study Builder is advantageous.
• Strong knowledge of case report form design, database programming, and study build processes.
• Understanding of drug development processes, Good Clinical Practices (GCP), and ICH guidelines.
• Highly organized, detail-oriented, and capable of managing multiple priorities in a fast-paced environment.
• Excellent verbal and written communication skills in English, with the ability to support cross-functional teams.

• Competitive salary and full-time permanent employment.
• Flexible work schedule and remote work opportunities.
• Comprehensive benefits package including medical, dental, vision, and retirement plans.
• Ongoing learning, professional development, and training programs.
• Supportive, collaborative, and stimulating work environment.
• Opportunities for career growth and advancement within the clinical research field.