Description
Clinical Data Programmer - Amsterdam - 9 Month Contract
Main Responsibilities:
- Computer programming position working with clinical trials data.
- Primary responsibilities include providing clinical data management and biostatistical programming support for various phases of clinical studies.
- Activities include importing/exporting data, reformatting raw data to CDISC and/or client specified analysis standards, programming and/or validating analysis data sets, tables, listings, graphs, ad hoc reports and regulatory submission deliverables such as ISS, ISE, and eCRT and Define documents.
- Assists Data Management and Biostatistics with developing tools and techniques for improving process efficiencies.
- Communicates effectively within a multi-disciplinary project team to complete assigned tasks on time and within budget.
- Contributes directly to the company's revenue by performing programming and validation of client deliverables in Data Management and Biostatistics.
- Successful completion of assigned tasks increases the likelihood of repeat business from the client and ongoing success in acquisition of new business.
Key Requirements:
- BA/BS degree or equivalent in computer science, statistics, biostatistics, mathematics or related field and at least two years of SAS programming experience and 1 year of clinical research or related experience or the equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills and abilities.
- Knowledge of one or more programming languages
- Knowledge of relational data base structure and experience working with complex data systems
- Experience demonstrating leadership ability and ability to work on a multi-disciplinary project team
- Ability to effectively organize and manage multiple assignments with challenging timelines
- Ability to mentor Associate Programmer in nuances of clinical trials programming.
If interested please respond with an updated C.V.