> Markdown version of [/jobs/ext/1556589-senior-pharmacovigilance-system-architect-argus-administrator-us](https://www.wearedevelopers.com/jobs/ext/1556589-senior-pharmacovigilance-system-architect-argus-administrator-us). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Senior Pharmacovigilance System Architect (Argus Administrator) - US - **Company:** MMS Holdings Inc - **Location:** Raleigh, NC, United States - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Clinical Data Repository, Databases, Linux, Systems Architecture, Information Technology - **Published:** July 16, 2026 - **Apply:** https://www.careerjet.com/jobad/us4eb7388495bf6d448d3870b7b3a64a60 ## About the Role * College graduate Information Technology discipline or related field, or relevant experience. * Minimum of 5 years' experience in Information Technology or similar field required. * Expert knowledge of scientific principles and concepts. * Reputation as emerging leader in field with sustained performance and accomplishment. * Proficiency with MS Office applications. * Hands-on experience with clinical trial and pharmaceutical development preferred. * Good communication skills and willingness to work with others to clearly understand needs and solve problems. * Excellent problem-solving skills. * Good organizational and communication skills. * Familiarity with current ISO 9001 and ISO 27001 standards preferred. * Familiarity with 21 CFR Part 11, FDA, and GCP requirements. * Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process. ## Description We are recruiting for an experienced Pharmacovigilance System Architect (Argus Administrator SME) to join our US team. Roles & Responsibilities * Serves as Database Administrator for Argus Safety, including database configuration, issue resolution, maintenance, governance and daily support. * Performs installations, upgrades, configuration of reporting rules, and E2B reporting via gateway technologies (including set-up and configuration of Axway Gateway Interchange). * Provides support for all systems associated with PV and drug safety. * Performs updates to Argus configuration and processes as per changing EudraVigilance regulations. * Provides support and execution of activities related to EudraVigilance testing for various clients. * Performs case migration/database transfers, file importing and supports other case processing activities. * Provides leadership in executing Argus upgrades and related activities. * Provides administrator support for other safety databases (such as ARISg). * Performs periodic coding dictionary (MedDRA & WHO drug) updates for Argus. * Provides technical assistance and support to Drug Safety Associate team with electronic submissions of serious adverse advents to European agencies. * Writes procedural documents including Standard Operating Procedures (SOP), Work Practice Documents, and Data Entry Manuals for Argus Safety. * Generates case processing metrics, reviews and makes suggestions and supports process improvement implementation. * Maintains technical expertise of regulatory requirements and ensures alignment with company working practices. * Assists with business development and capabilities efforts as needed. * Interacts directly and independently with client to coordinate all facets of projects; competent communicator, supports client capabilities as PV/drug safety systems SME. * Strong understanding and experience working with Argus configuration and study set up. * Strong understanding of global case processing and SAE reporting. * Strong understanding of global clinical trial development and data., Hi We are looking for Sr. Linux Admin for a long term contract in Raleigh, NC. Please reply back with your updated resume. 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