Clinical Programmer (m/f) 389802/11

November 2018

November 2019

CH-Basel

nicht angegeben

06.11.2018

389802/11

Projektbeschreibung

Ihre Aufgaben:
Lead and/or contribute to the development of the clinical study database and all components in collaboration with the Study Data Manager, who provides the core specifications
Development of reports and visualizations outputs for data cleaning, clinical narratives and reconciliation activities in collaboration with the Study Data Manager and other customers
Development of data transformation programs, including specifications according to CDISC and specific data tabulation standards
Select and implement appropriate study conventions, including data collection and data tabulation standards, knowledge sharing and best practices on assigned study(s)
Effectively communicate with SDM, study team, Functional Service Providers and stakeholders on Clinical Study Database, Reporting and Transformation requirements and status of work
Manage Clinical Programming deliverables, including timelines, risks and coordination of cross-functional tasks with strong understanding of downstream processes and stakeholder needs and impacts
Provide coaching and mentoring to clinical programming colleagues
Develop and maintain relationships with internal and external stakeholders

Ihre Qualifikationen:
BA/BS degree or equivalent and moderate industry-related experience
Programming competency
Ability to to be flexible and adaptable according to changing business priorities
Strong communication skills
Ability to keep to deadlines
Good understanding of the role of data management, biostatistics and statistical programming in the drug development process
In-depth understanding of the business of his or her discipline and the wider CDM organization


Projektstart: asap
Projektdauer: 12 MM++


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