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Clinical Data Programming Lead

Netherlands-Amsterdam
Permanent
Reference: 053709
This vacancy has now expired.
Description
Clinical Data Programming Lead - Netherlands (Amsterdam)
*LI-SS1
 
ICON is proud to announce the new partnership with one of the top Pharma’s in Europe. This new team will be based within the client’s offices based in Amsterdam with a dual mission “to help people do more, feel better and live longer.  Both organisations join together with a strong science and technology focus to deliver best in class solutions to the healthcare industry.
 
As the Clinical Data Programming Lead you will participate in the data management technical aspects of Clinical or Epidemiological studies which includes the development of specific tools to collect, monitor, clean and report study data.

 
About Clinical Data Programming Lead at ICON: 
 
In this central role, you will be responsible for supporting CDMS Programming activities as related to building study databases, system reports and configuring other system features. As a Clinical Data Programming Lead you can also function as a Team Lead for CDMS Programmers,  ensuring team delivers to expected quality and timelines and providing technical oversight and training/mentoring.
 
Responsibilities: 
  • Participates in study specific database set-up within at least one CDMS system (preferred Inform).
  • Reviews database specification documents created by study teams, such as CRF Specifications and Data Validation Specifications (DVS)
  • Creates/Programs edit checks, special actions and derivations as per a DVS.
  • Works closely with centralized CDMS Testing Group to ensure all programming issues are resolved in a timely manner and study timelines are met
  • Trouble-shoots and solves study building issues and edit check programming issues.
  • 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; ensure team achieves productivity and quality targets, perform benchmarking reviews and perform oversight of deliverables using different tools/ techniques and maintain and report relevant metrics.
  • Contributes to training materials on a process, system or technology level. Works with CTD and CDMS Management on delivery of training courses, instructor-led and on-the-job.
 
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 or other EDC system
  • Team player with strong verbal and written communication skills
  • Demonstrated ability to learn new technologies, applications and techniques
  • Understanding of database concepts.
Benefits of Working in ICON
 
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package.  This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
 
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.   
 
What’s Next?
 
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
 
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
 
 
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