Veeva CDMS Specialist

Job SummaryWe are seeking a skilled Clinical Systems Tester to join our team. The ideal candidate will have core expertise in Veeva CDMS (EDC) and hands-on experience with eCOA and IRT platforms.

Job Description:We are seeking a Clinical Systems Tester to support testing and validation activities within a Decentralized Clinical Trial (DCT) environment. The ideal candidate will have core expertise in Veeva CDMS (EDC) and strong hands-on experience with eCOA and IRT platforms.Responsibilities:Author and execute test scripts in Veeva EDC, aligned with...

Job Overview:We are seeking a detail-oriented regulatory affairs specialist to support the preparation of end-to-end submissions for global markets. Required exposure includes lifecycle management, Veeva Vault RIM, and complex initial and variation submissions.Key Responsibilities:

Job DescriptionWe are seeking a detail-oriented regulatory specialist to support end-to-end submissions for global markets. The successful candidate will have experience with lifecycle management, Veeva Vault RIM, and complex initial and variation submissions.Key Responsibilities:Prepare variation documents and/or evaluate post-approval changes in compliance...

Job Title: Clinical Quality Assurance SpecialistThe Clinical Quality Assurance Specialist will play a pivotal role in ensuring the highest standards of quality are met across ongoing clinical trials. This individual will serve as the primary QA support resource for clinical study teams, providing expertise in Good Clinical Practice (GCP) and internal quality...

Key Responsibilities:We are seeking a highly skilled Regulatory Publishing Specialist to prepare and manage BLA submissions in eCTD format using Veeva Vault eCTD Publishing.The ideal candidate will compile, format, and publish regulatory documents according to global health authority requirements.Strong attention to detail and excellent organizational skills...

Job Title: QA SpecialistThis is a full-time contract role offering 30–40 hours per week of consistent work. The contractor will act as a core member of the Quality Assurance function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.Key Responsibilities:Serve as the primary Quality Assurance resource for clinical...

Regulatory Publishing SpecialistManage BLA submissions in eCTD format using Veeva Vault eCTD Publishing.Ensure compliance with regulatory guidelines and internal processes.Compile, format, and publish regulatory documents according to global health authority requirements.Perform QC of eCTD submissions, including file structure, hyperlinks, and...

We are seeking a highly experienced QA professional to provide day-to-day clinical quality assurance (QA) support across ongoing clinical trials.Guide study teams, maintain compliance with Good Clinical Practice (GCP), and ensure quality oversight.Serve as the primary QA support resource for clinical study teams, ensuring compliance with GCP and internal...

We are looking for an experienced API Integration Specialist to design, build, and maintain robust API-based integrations across enterprise platforms. The ideal candidate has deep technical expertise in REST/SOAP APIs, middleware, and experience integrating applications in regulated environments such as life sciences or healthcare.???? Key...