clinical data manager programmer - data management in Neuchatel

posted
contact
Barbara Sorce, Basel Professionals Health Care & Life Sciences
job type
contract
apply now

job details

posted
location
neuchatel, neuchâtel
sector
Life Sciences
job type
contract
reference number
11824
contact
barbara sorce, basel professionals health care & life sciences
phone
058 201 55 50
apply now

job description

Our client, a leading international tobacco company, with seven of world’s top 15 brands, including the world’s number one brand is looking for a

Clinical Data Programmer - Data Management 

Location: Neuchâtel, Switzerland

Contract: 1 year with possibility of extension

Start Date: asap 

Job Description :

The Clinical Data Programmer (CDP) will be in charge of performing SAS programming to improve data management activities in the context of clinical studies. The CDP may also act as Clinical Data Manager as needed and works closely with the Clinical Study Team to supervise the CROs operational execution of the data management activities by monitoring the quality and timeliness of data management deliverables and ensuring that the data collection tools, data cleaning process and resulting data (including documentation of the process) are delivered according to the highest level of industry standards.

Responsabilities:

  • Perform SAS programming to provide complex listings/reports to support Data Management
  • Design and develop SAS macros, standard programs, applications and other utilities to expedite Data Management activities
  • Contribute to review data deliverables from the CRO to ensure the compliance of the study database with Clinical Data Interchange Standards Consortium (CDISC) and SDTM submission package requirements
  • Develop/improve internal processes and standards for data acquisition, data management and SDTM mapping
  • Oversee and monitor the CROs data management activities in accordance with the study level plan, track the progress of the study and evaluate the quality of the database from study set-up to database lock

Skills and Competencies:

  • Bachelor or Master Degree in Life Science
  • 2-5 years of SAS programming experience
  • 2+ years of Data Management / CRO oversight experience
  • Understanding and experience applying SDTM standards
  • Judgment skills to work accurately and efficiently toward quality result
  • Fluent in both written and oral English (German or French are an advantage)