Senior Clinical Data Programming Lead
il y a 3 semaines
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
-
Clinical Data Coordinator
il y a 7 jours
Leuven, Belgique HAYS Temps pleinClinical Data Coordinator | Full-time | CDI | English | Leuven | 1094059 Hays is looking for a Clinical Data Coordinator (CRO) to join our client data management team. **Your responsibilities as a Clinical Data Coordinator (CRO)** In this role, you will have the opportunity to put your analytical skills to use by validating database designs, reporting on...
-
Clinical Data Manager
il y a 3 semaines
Leuven, Belgique HAYS Temps pleinClinical Data Manager | Full Time | Healthcare | Leuven | 1091297 **Your responsibilities as a Clinical Data Manager**: - Develop and review data management procedures for clinical trials with sponsor companies and other departments; - Design reports and metrics that are useful management tools for your projects - Lead the design and validation of the CRF...
-
Data Manager
il y a 7 jours
Leuven, Belgique Medpace, Inc. Temps pleinJob Summary: Our corporate activities are growing rapidly, and we are currently seeking an office - based Clinical Data Manager to join our Belgian Data Management team in Leuven. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. This role takes on the responsibility as a leader in data...
-
Experienced Clinical Database Programmer
Il y a 4 mois
Leuven, Belgique Medpace, Inc. Temps pleinJob Summary: Our global business is growing rapidly, and we are currently seeking a full-time office-based Clinical Database Programmer to join our Data Management team in our Leuven office. This position will work in a team to develop databases in which clinical data are captured and processed for analysis and reporting. The role requires the ability to...
-
Clinical Data Coordinator Lab
il y a 7 jours
Leuven, Belgique HAYS Temps pleinClinical Data Coordinator | Full-time | CDI | English | Leuven | 1094058 Hays is looking for a Clinical Data Coordinator Lab to join our client data management team. **Your responsibilities as a Clinical Data Coordinator Lab** In this role, you will have the opportunity to play a crucial part in ensuring the accuracy and completeness of our data by...
-
Clinical Data Manager
il y a 3 jours
Leuven, Belgique Medpace, Inc. Temps pleinJob Summary: Our corporate activities are growing rapidly, and we are currently seeking a full-time, **office-based** **Clinical Data Manager** to join our Data Management team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous...
-
Clinical Database Programmer
il y a 3 semaines
Leuven, Belgique HAYS Temps pleinClinical Database Programmer | Full-time | Healthcare | Leuven | 1091299 **Your responsibilities as a Clinical Database Programmer**: - Setup, validate, and maintain study database systems in ClinTrak Lab; - Program edit checks, result reports, and label/tube type templates; - Program billing requirements within ClinTrak Lab; - Ensure programming study...
-
Clinical Database Programmer
Il y a 4 mois
Leuven, Belgique Medpace, Inc. Temps pleinJob Summary: Our global business is growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Data Management team in our Leuven office. The position will work in a team to develop databases in which clinical data are captured and processed for analysis and reporting. This position plays a critical role...
-
Experienced Clinical Database Programmer
il y a 2 semaines
Leuven, Belgique NonStop Consulting Temps pleinExperienced Clinical Database Programmer My Client who is a very successful, mid-size CRO are currently looking for an Experienced Clinical Database Programmer to join their team on a Hybrid bases in one of three locations; Leuven(Belgium), Milan(Italy) or Rotterdam(Netherlands). They are constantly growing, which allows for your personal growth as well as...
-
Experienced Clinical Database Programmer
il y a 2 semaines
Leuven, Belgique Medpace, Inc. Temps pleinJob Summary: Our global activities are growing rapidly, and we are currently seeking a full-time, office/home-based** Experienced Clinical Database Programmer** to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your...
-
Clinical Database Programmer
il y a 2 semaines
Leuven, Belgique Medpace, Inc. Temps pleinJob Summary: Our global activities are growing rapidly, and we are currently seeking a full-time, office-based **Clinical Database Programmer - Entry** to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous...
-
Clinical Data Coordinator Lab
il y a 3 semaines
Leuven, Belgique Medpace, Inc. Temps pleinJob Summary: - We are currently seeking a full-time, office-based Data Coordinator for our Medpace Reference Laboratories to join our Data Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop...
-
Clinical Trial Lead
il y a 2 semaines
Leuven, Belgique PSI CRO Temps pleinCompany Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,300 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...
-
Clinical Trial Lead
il y a 1 semaine
Leuven, Belgique PSI CRO Temps pleinCompany Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,300 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...
-
Team Leader Data
Il y a 7 mois
Leuven, Belgique Twipe Mobile Solutions Temps plein**Team Leader Data & AI**: Twipe is a mediatech scale-up based in Leuven, Belgium working with leading newspaper publishers in Europe and the US to grow their digital subscribers and sustain quality journalism. We offer cloud based digital edition publishing, analytics, and personalization solutions. Our innovative solutions accelerate the growth of...
-
Biostatistician & SAS Programmer
Il y a 4 mois
Leuven, Belgique Terumo Europe Temps pleinAt Terumo, we enhance lifesaving medical technologies for the benefit of society. Are you eager to contribute to people's health and patients' wellbeing? We'll challenge you to become a master in your field of expertise. You can invest your talents in balance with your personal aspirations - live and work in harmony. Built on our Japanese origins; we are...
-
Scientist Clinical Laboratory
il y a 7 jours
Leuven, Belgique Medpace, Inc. Temps pleinJob Summary: Responsibilities: - Monitor laboratory operations in order to verify that accurate, precise, and medically-reliable data are being generated; - Interact with corporate leadership, administration, government agencies, accrediting agencies, and potential sponsors/clients to gain information and knowledge required to make appropriate business...
-
(Senior) Clinical Project Manager
il y a 2 semaines
Leuven, Belgique PSI CRO Temps pleinCompany Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. **Job Description**: Home-based or Office-based **Your...
-
(Senior) Clinical Project Manager
il y a 2 semaines
Leuven, Belgique PSI CRO Temps pleinCompany Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description Home-based or Office-based **Your...
-
Senior Medical Science Specialist
il y a 4 semaines
Leuven, Flanders, Belgique Terumo Europe NV Temps pleinTaken en verantwoordelijkhedenDepartment InfoTerumo develops products for interventional radiologists that specialize in treating patients with oncological indications. Rising to the challenge of creating innovative treatments for patients, we bring you a complete range of interventional oncology products that focus on Access, Loco-regional treatments and...