ALTEN MAROC, a branch of the world leader in engineering and technology consulting founded in 2008 and present in Fès, Rabat, Tétouan, and Casablanca, now has over 2200 employees and aims for a center of excellence of 3300 ALTENiens by the end of 2027. It is now a strategic player in supporting the professional development of engineers.
Our mission: to meet the technological ambitions of our clients - major international contractors - in the automotive, rail, R&D and IT, telecommunications, and media sectors.
Joining ALTEN Maroc means joining an ecosystem of excellence and benefiting from:
• A personalized and evolving career path
• An ambitious skills development policy
• A stimulating, collaborative, and meaningful work environment
Discover the testimony of Hajar Bououd, HR Director and Communications at ALTEN Maroc in Challenge Maroc magazine by clicking here: https://bit.ly/3QMntIc
Company culture :
Alten Maroc is defined by a deeply collaborative culture, focused on people, trust, and strong team support, with hands-on managers who guide and develop talent.
This environment is enhanced by a strong drive for innovation, encouraging creativity, initiative, and experimentation across projects.
A structured and disciplined organization ensures efficiency, rigor, and quality in engineering delivery. Performance and ambition are part of the culture as well, supporting collective success while maintaining a positive and caring atmosphere.
Job :
The Access Management Specialist is responsible for the administration and support of clinical systems and Oracle-based platforms. The role ensures secure user access management, system validation compliance, user support, and continuous improvement of clinical applications used throughout clinical trial activities.
System Administration & Access Management
Manage user access and permissions across multiple clinical applications (EDC, eTMF, and other clinical systems).
Ensure compliance with access management processes and security requirements.
Support onboarding, modification, and removal of user accounts.
System Validation & Compliance
Maintain the validated state of clinical systems.
Develop, execute, and document validation test scripts.
Ensure compliance with Computerized System Validation (CSV) requirements.
Support audits and quality reviews related to system validation activities.
User Support & Incident Management
Provide Level 2 support to clinical users.
Investigate, troubleshoot, and resolve system-related issues.
Track and manage support requests through ticketing systems.
Monitor recurring issues and propose improvement actions.
Requirements & Continuous Improvement
Collect and document user requirements for system enhancements.
Act as a liaison between business users and technical teams.
Participate in team meetings and contribute to system improvement initiatives.
Support the implementation of new functionalities and process enhancem
Required profile :
Master's Degree in Engineering, Computer Science, Life Sciences, or a related scientific field.
2 to 5 years of experience in clinical systems administration, access management, or clinical trial support environments.
Technical Skills
Experience in clinical trial system administration and support.
Knowledge of clinical research processes and regulations, including ICH-GCP/GxP.
Understanding of Computerized System Validation (CSV) methodologies.
Experience with user access management and application administration.
Knowledge of eTMF, EDC, and other clinical trial systems.
Previous experience with Oracle solutions is highly desirable.
Familiarity with ticketing and issue-tracking tools.
Soft Skills
Strong communication and interpersonal skills.
Excellent listening and user support capabilities.
Ability to explain technical concepts to non-technical users.
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