ppWe are seeking an experienced IT Business Partner to serve as the strategic technology liaison for our Medical Affairs, Regulatory Affairs, Clinical Development, and Drug Safety (Pharmacovigilance) functions. This individual will partner closely with business leaders to shape technology roadmaps, drive digital transformation initiatives, and optimize enterprise platforms that support the end-to-end pharmaceutical product lifecycle. /p h3About the Role /h3 pThe successful candidate will possess deep knowledge of the pharmaceutical industry and hands-on experience with Veeva platform solutions and Pharmacovigilance/Safety systems, enabling them to bridge business objectives with technology capabilities while ensuring compliance with global regulatory requirements. /p h3Responsibilities /h3 ul libStrategic Business Partnership /b /li liAct as the trusted technology advisor to Medical, Regulatory, Clinical Operations, and Pharmacovigilance stakeholders. /li liDevelop strong relationships with executive and functional leaders to understand business priorities, challenges, and opportunities. /li liTranslate business strategies into technology roadmaps and investment plans. /li liLead demand management, prioritization, and governance processes across the business portfolio. /li liDrive the strategy, adoption, optimization, and lifecycle management of key GxP-regulated applications. /li liOversee technology solutions supporting: /li liClinical Development /li liClinical Operations /li liRegulatory Affairs /li liMedical Affairs /li liPharmacovigilance and Drug Safety /li liEnsure alignment between enterprise architecture, data, integration,



and business objectives. /li liProvide leadership and strategic oversight across Veeva solutions, including: /li liVeeva Medical CRM /li liPartner with business teams to identify opportunities for process automation, standardization, and optimization. /li libPharmacovigilance Safety Systems /b /li liSupport and enhance general drug safety platforms and processes. /li liCollaborate with Safety, Regulatory, and Quality teams to ensure compliance with health authority requirements. /li liExperience with one or more of the following is highly desirable: /li liOracle Argus Safety /li liArisGlobal LifeSphere /li liSafety databases and case processing solutions /li liDrive initiatives related to safety reporting, signal detection, risk management, and regulatory submissions. /li liLead complex cross-functional transformation programs from strategy through implementation. /liliManage technology vendors, system integrators, and consulting partners. /li liEnsure projects are delivered on time, within budget, and meeting quality and compliance requirements. /li liOversee change management, communications, training, and stakeholder adoption activities. /li libCompliance Governance /b /li liEnsure solutions comply with:



/li liGxP /li liFDA regulations /li liEMA guidelines /li liICH standards /li li21 CFR Part 11 /li liData privacy requirements (GDPR and applicable regulations) /li liSupport validation and audit activities for regulated systems. /li /ul h3Qualifications /h3 ul liBachelor's degree in Information Technology, Computer Science, Life Sciences, Pharmacy, or related discipline. /li li8+ years' experience in IT Business Relationship Management, IT Business Partnering, Digital Transformation, or Enterprise Applications within the pharmaceutical or life sciences industry. /li /ul h3Required Skills /h3 ul liStrong understanding of: /li liClinical Development /li liRegulatory Affairs /li liMedical Affairs /li liProven experience delivering and supporting enterprise platforms in regulated environments. /li liDemonstrable experience with the Veeva Suite, ideally including Vault Clinical and Vault RIM. /li liExperience with Pharmacovigilance platforms such as Argus, LifeSphere, or Veeva Safety. /li liStrong knowledge of application integration, data management, and enterprise technologies. /li liExperience managing external vendors and technology partners. /li /ul h3Preferred Skills /h3 ul liExperience supporting global pharmaceutical or biotechnology organizations. /li liUnderstanding of RD digital ecosystems and clinical trial technologies. /li liExperience with cloud platforms and SaaS application delivery models. /li liKnowledge of AI, automation, and advanced analytics applications within Life Sciences. /li /ul /p #J-18808-Ljbffr

📌 Information Technology Business Partner (Barcelona)
🏢 Planet Pharma
📍 Barcelona