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4 giorni fa
TN Italy is seeking a highly skilled Clinical Trial Programming Expert to join our team. As a Clinical Trial Programming Expert, you will be responsible for developing SAS programs for generating datasets, tables, figures and listings for clinical studies under the supervision of the Direct Manager.
Main Responsibilities:
- Collaborating with Biostatistics and Data Management staff on clinical trials/projects.
- Developing SAS programs for generating datasets, tables, figures and listings for clinical trials.
- Using CDISC guidelines to generate SDTM/ADaM datasets.
- Writing Programming Specifications of analysis datasets.
Required Skills and Qualifications:
- Scientific degree.
- At least 1 year of experience in CRO, biotech, pharma, research institutes in a similar role is preferred.
- Knowledge of HA requirements pertaining to pharmaceutical research and specifically to SAS programming.
- Knowledge in statistics and its applications to clinical trials.
- Knowledge of SAS and CDISC standards (SDTM, ADaM).
- Fluent in English.
About Us:
OPIS is an International CRO with 25 years of experience in conducting Phase I-IV, non-interventional and medical devices studies on an international level. We always offer state-of-the-art information technology solutions and innovative approaches to the increasing complexity and variety of projects.
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