Solutions Expert – Clinical Data Acquisition
Il y a 4 heures
belgium belgium
MSI Pharma
Temps plein
Gratuit avec email ou Google
Enregistrez cette offre et organisez votre recherche
Créez un compte gratuit pour enregistrer des offres d'emploi, créer des alertes et revenir à cette liste depuis votre tableau de bord.
Gratuit avec email ou Google
En continuant, vous acceptez nos Conditions d’utilisation & Politique de confidentialité.
ppbIT Solution Expert
- Clinical Data Acquisition Systems /b | bLocation: Brussels Region, Belgium (Hybrid) /b | bEngagement: Freelance /b | bClient: Biopharma /b | Competitive hourly rate available /p pWe are supporting a major biopharma organisation in hiring an bIT Solution Expert /b to provide end‑to‑end support, maintenance, and enhancement of their bprimary clinical data acquisition platforms /b, including a suite of Medidata solutions and Trial Grid. You will act as the technical owner for system updates, validation activities, incident management, and change control while collaborating with internal teams and external platform providers. This is a high‑impact role supporting global clinical development operations. /p h3Key Responsibilities /h3 ul liProvide ongoing bsupport and maintenance /b for the organization’s Clinical Data Acquisition platform (incl. Medidata iMedidata, Rave, Coder, Cloud Admin and Coder+). /li liSupport and maintain the bTrialGrid /b system used to validate clinical study builds. /li liAssess the impact of new Medidata and TrialGrid product releases on availability, security, interfaces, and maintenance requirements. /li liDrive bIT changes /b, including updates to computerized system validation documentation, IQ/OQ testing, and implementation of new/changed user requirements. /li liPerform baccess management /b for designated user roles. /li liCollaborate with SMEs to resolve bincidents /b in alignment with ITIL best practice. /li liSupport the bperiodic review /b of Clinical Data Acquisition and TrialGrid systems. /li /ul h3Requirements /h3 h3Education /h3 ul liBachelor’s degree (minimum) in bComputer Science /b or a related field. /li /ul h3Experience Technical Skills /h3 h3Mandatory /h3 ul liDirect experience with bMedidata platforms /b (e.g., iMedidata, Cloud Admin, Rave, Coder). /li liProven experience in bcomputerized systems validation /b (CSV). /li liExperience in bcomputerized system testing /b. /li liStrong background in bIT change management /b. /li liExperience handling baccess management /b. /li /ul h3Preferred /h3 ul liExperience with bTrialGrid /b. /li liITIL‑aligned bincident management /b experience. /li liBackground in the bpharmaceutical industry /b (3+ years preferred). /li liKnowledge of bClinical Development /b processes. /li /ul h3Soft Skills /h3 ul liFluent in bEnglish /b (written and spoken). /li liStrong btechnical documentation /b writing skills. /li /ul pExcellent bteam collaboration /b abilities. /p /p
- Clinical Data Acquisition Systems /b | bLocation: Brussels Region, Belgium (Hybrid) /b | bEngagement: Freelance /b | bClient: Biopharma /b | Competitive hourly rate available /p pWe are supporting a major biopharma organisation in hiring an bIT Solution Expert /b to provide end‑to‑end support, maintenance, and enhancement of their bprimary clinical data acquisition platforms /b, including a suite of Medidata solutions and Trial Grid. You will act as the technical owner for system updates, validation activities, incident management, and change control while collaborating with internal teams and external platform providers. This is a high‑impact role supporting global clinical development operations. /p h3Key Responsibilities /h3 ul liProvide ongoing bsupport and maintenance /b for the organization’s Clinical Data Acquisition platform (incl. Medidata iMedidata, Rave, Coder, Cloud Admin and Coder+). /li liSupport and maintain the bTrialGrid /b system used to validate clinical study builds. /li liAssess the impact of new Medidata and TrialGrid product releases on availability, security, interfaces, and maintenance requirements. /li liDrive bIT changes /b, including updates to computerized system validation documentation, IQ/OQ testing, and implementation of new/changed user requirements. /li liPerform baccess management /b for designated user roles. /li liCollaborate with SMEs to resolve bincidents /b in alignment with ITIL best practice. /li liSupport the bperiodic review /b of Clinical Data Acquisition and TrialGrid systems. /li /ul h3Requirements /h3 h3Education /h3 ul liBachelor’s degree (minimum) in bComputer Science /b or a related field. /li /ul h3Experience Technical Skills /h3 h3Mandatory /h3 ul liDirect experience with bMedidata platforms /b (e.g., iMedidata, Cloud Admin, Rave, Coder). /li liProven experience in bcomputerized systems validation /b (CSV). /li liExperience in bcomputerized system testing /b. /li liStrong background in bIT change management /b. /li liExperience handling baccess management /b. /li /ul h3Preferred /h3 ul liExperience with bTrialGrid /b. /li liITIL‑aligned bincident management /b experience. /li liBackground in the bpharmaceutical industry /b (3+ years preferred). /li liKnowledge of bClinical Development /b processes. /li /ul h3Soft Skills /h3 ul liFluent in bEnglish /b (written and spoken). /li liStrong btechnical documentation /b writing skills. /li /ul pExcellent bteam collaboration /b abilities. /p /p