Clinical Solutions Associate
Il y a 1 heure
Brussels, Belgique
Planet Pharma Group
Temps plein
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h3Clinical Solutions Associate /h3 pHelp shape the systems and data that enable high-quality clinical development worldwide. In this role, you’ll work across clinical applications, data repositories and global teams to improve data quality, streamline processes and support better decision‑making. /p h3Overview /h3 pWe’re seeking an experienced Clinical Solutions Associate to provide oversight of clinical applications, system integrations and data repositories within a global pharmaceuticalenvironment. You’ll partner with Clinical Sciences and Operations, Information Technology and stakeholders across functions to support system changes, reporting, validation and continuous improvement. /p h3Key Responsibilities /h3 ul liOversee clinical applications and repositories, including CTMS, eTMF, EDC/TMS, CDR, EDMS, BI tools and dashboards. /li liSupport system upgrades and change requests throughout the system development life cycle, from requirements gathering through implementation, training and maintenance. /li liDocument business outcomes, data integrations and service-level expectations. /li liProvide operational reporting and dashboards to help clinical teams identify data issues, review study and programme metrics, and analyse activity across projects and trials. /li liCollaborate with IT and global teams on planning, prioritisation, system documentation and validation. /li liLead or contribute to workstreams, taskforces and stakeholder meetings focused on improving processes and reducing duplication. /li liEvaluate new technologies and advise on their potential business value, risks and benefits. /li liSupport audits and inspections, and provide training, mentoring and guidance as needed. /li /ul h3Must-Have /h3 ul liAt least five years’ experience in a pharmaceutical or CRO setting. /li liAt least three years’ relevant experience in clinical data or technology within Drug Development or Life Sciences. /li liExperience with clinical systems such as EDC, CTMS, TMF, MDR/CDR, COAR, BI reporting or dashboards, and system integrations. /li liThree years’ GxP and system validation experience. /li liKnowledge of clinical processes, technical frameworks, Good Clinical Practice and Good Clinical Data Management Practices. /li liStrong project management, problem‑solving, organisation and communication skills. /li liProficiency in English and the ability to collaborate effectively with global teams. /li liExperience creating processes, SOPs or related documentation. /li /ul pBring your clinical technology expertise to a role with global impact– /p