Job Description

Please share your updated profile if you are interested in the below role.

Our client seeks an Veeva Admin for a 12 Months project in Remote . Below is the detailed requirement

Job Title: Veeva Admin

Work location : Remote

Duration: Long term Contract

Job Description:

• Bachelor's degree preferably in Computer Science, Information technology, Computer Engineering, or related IT discipline or equivalent experience with 12+ Minimum Experience

Nature and Scope of Job


We are seeking an experienced Veeva Database Manager with strong expertise in clinical data standards to join our Biomedical Data Stewardship team. This role is responsible for contributing to the design of clinical trial databases within Veeva Clinical Data Management System (CDMS), ensuring compliance with internal data collection standards and supporting high-quality data entry for clinical trials.

Qualifications

• 5+ years of experience in Clinical Data Management, with at least 2+ years managing Veeva CDMS databases.
• Strong knowledge and hands-on experience with CDISC CDASH implementation; exposure to SDTM a plus.
• Proven track record of building and maintaining clinical trial databases in compliance with regulatory and industry standards.
• Strong understanding of clinical trial processes, ICH-GCP, and regulatory requirements.
• Excellent problem-solving, communication, and cross-functional collaboration skills.
• Experience with other EDC platforms (e.g., Medidata Rave, Oracle InForm) in addition to Veeva.
• Familiarity with data visualization and analytics tools (e.g., Spotfire, SAS, R).
• Experience working in global teams within a pharmaceutical, biotechnology, or CRO environment.
• Knowledge of data exchange standards (e.g., CDISC ODM, Define.xml).

Primary Responsibilities

• The ideal candidate will have hands-on experience programming clinical trial databases, applying CDISC/CDASH standards, and collaborating with cross-functional teams including Clinical Operations, Biostatistics, and Regulatory Affairs.
• Key Responsibilities
• Consult on the design of electronic data capture (EDC) databases using Veeva CDMS.
• Review current RAVE DES data-collection specifications and propose Veeva CDMS structures.
• Ensure alignment with CDISC, CDASH, SDTM, and related industry standards for clinical data collection and reporting, as needed.
• Maintain and update standard libraries, forms, edit checks, and controlled terminology in line with evolving regulatory guidance.
• Work closely with Biostatistics, Clinical Programming, Safety, and Data Management to ensure smooth data flow and integration across systems.
• Develop and maintain documentation, including standard database specifications, edit check programming guides, and controlled terminology.

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