Reporting Programmer (Clinical Data)

Poste The Reporting Programmer is responsible for ensuring that the reporting environment meets the needs of Clinical Study Teams by gathering requirements, analyzing reporting requests, coordinating with business and technical stakeholders, and delivering high-quality reports and dashboards that support clinical decision-making.

Requirements Gathering & Business Analysis

Collaborate with Study Management, Clinical Data Management, and other stakeholders to identify reporting needs. Collect, analyze, and document requests for new reports, dashboards, enhancements, and modifications. Understand the business objectives and intended use of each reporting request. Identify target users and define the decision-making processes supported by reports. Assess existing reporting solutions before initiating new developments. Define report scope, timelines, study population, data sources, refresh frequency, and delivery methods. Stakeholder Management & Coordination

Facilitate requirement-gathering workshops and meetings with business stakeholders. Act as the interface between business teams and technical experts. Ensure proper communication and alignment between stakeholders throughout the project lifecycle. Maintain end-to-end traceability of reporting requests from submission through implementation. Reporting Development & Documentation

Produce detailed report specifications and functional requirements. Support the implementation and enhancement of reports and dashboards. Maintain reporting documentation and ensure consistency across deliverables. Prepare and distribute meeting minutes and follow-up action plans. Ensure delivered reports meet business expectations and quality standards.

Profil recherché Master's Degree in Science, Engineering, Computer Science, Data Management, or a related field. 2 to 5 years of experience in clinical reporting, clinical data management, or a related environment. Technical Skills

Experience in clinical trial reporting environments. Knowledge of clinical research processes and clinical trial data management. Understanding of Computerized System Validation (CSV) principles. Experience in business requirements gathering and documentation. Ability to understand complex system architectures and data flows. Previous experience with Oracle solutions is highly desirable. Knowledge of reporting and dashboarding tools is an advantage. Soft Skills

Excellent communication and listening skills. Strong analytical and problem-solving abilities. Solution-oriented mindset. Strong organizational and stakeholder management skills. Ability to work in cross-functional and international environments. Open-mindedness and adaptability.

Entreprise ALTEN MAROC , Filiale du leader mondial de l’ingénierie et du conseil en technologie créé en 2008 et présent à Fès, Rabat, Tétouan et Casablanca, compte aujourd’hui plus de 2200 collaborateurs et vise un centre d’excellence de 3300 ALTENiens en fin 2027 . Elle s’impose aujourd’hui comme un acteur stratégique dans l’accompagnement du développement professionnel des ingénieurs.

Notre mission : répondre aux ambitions technologiques de nos clients — grands donneurs d’ordre internationaux — dans les secteurs de l’automobile, du ferroviaire, de la R&D et de l’IT, des télécommunications et des médias.

Rejoindre ALTEN Maroc, c’est intégrer un écosystème d’excellence et bénéficier :

• D’un parcours de carrière personnalisé et évolutif

• D’une politique ambitieuse de développement des compétences

• D’un environnement de travail stimulant, collaboratif et porteur de sens

Découvrez le témoignage de Hajar Bououd , DRH et Communication chez ALTEN Maroc dans le magazine Challenge Maroc en cliquant ici : https://bit.ly/3QMntIc