Beschreibung
You are an expert in the area SAS Programming?I am currently looking for our Client a CRO in South Germany.
Please find below what our client requests:
Main Duties and Responsibilities
*Lead and support worldwide statistical programming activities for assigned project area for clinical trials
* Function as lead statistical programmer with respect to all statistical programming activities for multiple clinical trials or submissions
* Set-up and oversee a clinical project or trial. Support to enable delivery of high quality statistical programming work product
* Generate SAS-datasets and tables, figures, listings, and documentation for clinical study reports, ad hoc requests, and regulatory submissions
* Produce submission ready electronic datasets, tables, figures, listings and documentation that support and match planned work product and are sufficient to respond quickly to questions by regulatory authorities
* Interact with project or trials teams and other departments to ensure delivery of high quality statistical programming services and work product
* Ensure deadlines for projects
Experience and Knowledge
Essential Skills
* several years experience in statistical programming, minimum 5 years in the Parmaceutical Induystry
* expert knowledge of SDTM and SDTM/ ADaM programming requirements and practices
* strong communication and mentor skills
* excellent project and time management skills
* Oncology experience
Qualifications
* Master Applied Informatics
Language Skills
Fluent in English
Framework Condition:
Start Date: asap
Duration: 12 Months, onsite
You know that one of your colleagues is looking for a new project?
Also if you know somebody who would be interested in this position, then please contact me. If we successfully place an applicant that you have recommended, you will receive an EUR 250, voucher of "Jochen Schweizer".
Kind regards,
Jelena Stupar , Progressive Recruitment
Consultant Pharma: Clinical Data Management, Biostatistics and SAS Programming
Phone: