Senior Clinical Data Programming Lead

il y a 3 semaines


Leuven, Belgique Icon plc Temps plein

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

We have an incredible opportunity for a Senior Clinical Data Programming Lead to join the team.

Summary

The Clinical Data Programming Lead/Senior Lead (CDPL) is part of the Clinical Data Management Systems (CDMS) group. In this central role, you will be responsible for building and maintaining EDC databases using Medidata Rave. You will act as a Team Lead and SME for Rave Programmers and Testers ensuring team delivers to expected quality and timelines and providing technical oversight and training/mentoring.

Location Options

EMEA - office or home based working

**Responsibilities**:

- Leads study specific database build using Medidata Rave.
- Design CRFs and Program edit checks, Custom Functions, Derivations, etc. Set up Coder, Lab, IRT, T-SDV, and Rave Safety Gateway integrations.
- Serves as Team lead to CDMS Programmers, providing training, best practices, support and quality checks on study build and programming; ensure effective resource allocation and workload balancing across assigned team members
- Extend technical expertise and mentor team members on an ongoing basis

To succeed you will need

The successful individual will have a proven experience in study build set up; possess a strong understanding of the principles of system development lifecycle and governance and be able to perform assigned tasks with minimum supervision.
- Prior relevant experience in building study databases
- Ability to successfully manage multiple tasks and timelines
- Experience in Medidata Rave (Medidata certification is preferred)
- Team player with strong verbal and written communication skills
- Understanding of database concepts

Benefits of Working in Icon

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

__________________________________

ICON plc est un leader mondial en matière de soins de santé intelligents et de recherches cliniques. De la molécule au médicament, nous faisons progresser la recherche clinique en fournissant des services externalisés à des entreprises pharmaceutiques, biotechnologiques, de fabrication de dispositifs médicaux et à des organismes gouvernementaux et de santé publique.

Grâce à nos patients qui sont au centre de tout ce que nous faisons, nous contribuons à accélérer le développement de médicaments et dispositifs médicaux qui sauvent des vies et améliorent la qualité de vie.

Nos employés constituent notre plus grand atout, au cœur de notre culture, ils représentent la force motrice de notre réussite. Les employés d’ICON ont pour mission de réussir et sont animés d’une passion qui garantit que ce que nous faisons, nous le faisons bien.

Nous avons une formidable occasion pour un Responsable de la programmation des données cliniques (RAVE) ou de joindre l’équipe.

Lieu :(à domicile OU dans nos bureaux)
- États-Unis
- Canada
- Mexico

Sommaire des responsabilités:
Ce Responsable de la programmation des données cliniques (RPDC) ou ce RPDC principal fait partie de l’équipe qui travaille avec les systèmes de gestion des données cliniques (SGDC). Dans ce rôle central, vous serez responsable de la création et de la gestion des bases de données acquises de façon électronique en utilisant le système Medidata Rave. Vous agirez en tant que chef d’équipe et d’expert en la matière pour les programmeurs et les vé


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