Manager, CTSM, Supply & Data Integration

Jobtailor; Mainz; Vor Ort; EUR 70.000 - 98.000; Vollzeit

Zusammenfassung

Jobtailor in Mainz, Germany seeks an experienced Clinical Trial Supply Management specialist to drive SAP S/4HANA implementations and ensure compliant data governance across regulated environments.

You will collaborate with cross-functional teams to align CTSM processes with business needs, own SAP/ICSM URS validation, and manage master data integration projects from planning through transformations.

Qualifikationen

• Completed university degree in a related field such as Engineering, Clinical Supply Chain Management, Quality Management, Computer Science, or Information Systems.
• Minimum 3 years of experience in Clinical Trial Supply Management within pharmaceutical/biotech or regulated industries; experience with system providers is an advantage.
• Expertise in ERP/IT implementation projects such as SAP S/4HANA; familiarity with ICSMSAP modules and third-party data integration concepts.
• Proven skills in executing SAP-supported clinical supply processes like material management, demand/supply planning, and logistics using tools like Kinaxis, ICSV, IRT or Veeva.
• Strong project management abilities paired with excellent organizational and communication skills for stakeholder engagement.
• Fluency in English (business-professional level); German proficiency is highly desirable.

Aufgaben

• Support the deployment and optimization of CTSM digital ecosystem, including SAP S/4HANA, IRT, and vendor platforms.
• Collaborate with the CTSM Global Template Process Owner by aligning SAP value streams with business needs through cross-functional collaboration.
• Identify ICSMSAP workflow requirements while harmonizing business needs with system capabilities for efficient execution.
• Act as the business process owner representative for SAP/ICSM system URS validation processes.
• Manage projects related to CTSM master data and integration; resolve issues, implement data governance practices, and optimize processes during transformations.

Kenntnisse

Clinical Trial Supply Management

SAP S/4HANA

Project Management

Data Governance

Stakeholder Engagement

Ausbildung

Related field degree (Engineering, Clinical Supply Chain Management, Quality Management, Computer Science, Information Systems)

Tools

Kinaxis

IRT

Veeva

ICSV

Jobbeschreibung

• Support the deployment and optimization of the CTSM digital ecosystem, including S/4HANA, IRT, and vendor platforms
• Collaborate with the CTSM Global Template Process Owner by aligning SAP value streams (e.g., I2R, S2S, MDM) with business needs through cross-functional collaboration
• IdentifyICSMSAP workflow requirements while harmonizing business needs with system capabilities for efficient execution
• Act as the business process owner representative for SAP/ICSM system URS validation processes
• Manage projects related to CTSM master data and integration; resolve issues, implement data governance practices, and optimize processes during transformations

Requirements

• Completed university degree in Engineering, Clinical Supply Chain Management, Quality Management, Computer Science, Information Systems, or related field
• Minimum 3 years of experience in Clinical Trial Supply Management within pharmaceutical/biotech or regulated industries; experience with system providers is an advantage
• Expertise in ERP/IT implementation projects such as SAP S/4HANA; familiarity withICSMSAP modules and third-party data integration concepts
• Proven skills in executing SAP-supported clinical supply processes like material management, demand/supply planning, and logistics using tools like Kinaxis, ICSV, IRT or Veeva
• Strong project management abilities paired with excellent organizational and communication skills for stakeholder engagement
• Fluency in English (business-professional level); German proficiency is highly desirable.

Core Competencies

Demonstrates expertise in Clinical Trial Supply Management and SAP S/4HANA implementation, with a strong focus on optimizing processes and managing data governance in regulated industries. Proven ability to collaborate cross-functionally and engage stakeholders effectively.

Highest-signal resume keywords

• Clinical Trial Supply Management
• SAP S/4HANA Implementation
• Project Management
• Data Governance Practices
• Stakeholder Engagement

ATS Optimization Keywords

Hard Skills

• ERP Implementation
• ICSM Modules
• Material Management
• Demand/Supply Planning
• Logistics

Soft Skills

• Organizational Skills
• Communication Skills

Industry Keywords

• Pharmaceutical
• Biotech
• Regulated Industries

Tools & Technologies

• Kinaxis
• IRT
• Veeva