Remote Veeva Clinical Data Programmer

Celerion; United States; On-site; USD 110,000 - 160,000; Full time

Job summary

Celerion is seeking a full-time Veeva Clinical Database Programmer to administer EDC databases, design eCRFs, and manage deployment of EDC trials in a remote environment.

The role requires expertise in Veeva EDC and Veeva CDB, with SQL programming and strong knowledge of CDISC standards to ensure data integrity across global clinical trials.

Collaboration with data management teams and vendors to meet regulatory timelines is essential.

Qualifications

• Bachelor's degree preferred.
• 3 years of clinical data management experience.
• Ability to program using SQL.
• Experience with Veeva EDC and Veeva CDB.
• Proficient computer skills with an understanding of clinical systems and data administration.

Responsibilities

• Serve as a subject matter expert in Veeva Clinical Data Management Suite, including Veeva EDC and CDB.
• Perform eCRF design and EDC build programming for assigned projects, including edit check programming.
• Maintain global clinical trial database standards (CDISC) and ensure secure database imports from vendor transfers.

Skills

SQL

Clinical data management

Veeva EDC

Veeva CDB

Data administration

Education

Bachelor's degree

Tools

Veeva EDC

Veeva CDB

Job description

Celerion is seeking a full-time Veeva Clinical Database Programmer to administer EDC databases, design eCRFs, and manage deployment of EDC trials in a remote environment.

The role requires expertise in Veeva EDC and Veeva CDB, with SQL programming and strong knowledge of CDISC standards to ensure data integrity across global clinical trials.

Collaboration with data management teams and vendors to meet regulatory timelines is essential.