Zurück zur Suche.SEC Recruitment Ltd - Senior SAS Programmer - Berlin, Germany
| Beschäftigungstyp: | Permanent |
| Standort: | Berlin, Germany |
| Gehalt: | |
| Sprachen: | Englisch, Deutsch |
Details für die Anzeigenschaltung
- Name:SEC Recruitment Ltd
- Veröffentlichung:08-08-2010
- Code:700SECLYBSASDE
Our client is an international company located in Berlin and seeking a permanent Senior SAS Programmer to join the programming team. For more information, please contact Louise Beka.
Our client covers a wide range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. In addition, they play a key part in the launching and development of some of the most important drugs.
As a Senior Programmer you will provide technical expertise for the conduct of clinical trials, act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to clinical systems, and/or analysis and reporting, and/or the applications/systems within eClinical technologies.
In addition, you will meet the requirements of a Programmer with a high degree of proficiency and autonomy; you will deliver best value with high quality service; coordinate projects and liaise with sponsors.
Your key responsibilities will include:
• Coordinate project start-up activities, creation of global programs, tracking spreadsheets, and required documentation;
• Assist in the production and QC of analysis plans, TLF, derived dataset specifications, programming specifications, and other process supporting documents;
• Use efficient programming techniques to produce and/or QC derived datasets tables, figures and data listings;
• Understand regulatory requirements concerning industry technical standards;
• Create standard macros and applications to improve the efficiency of the department
You have the following profile and experience:
• BA/BSc/MSc in Computer Sciences or equivalent;
• Minimum 4+ years experience as a SAS programmer;
• Fluent in English (spoken and written);
• Relevant Clinical Trial industry experience;
• Experience working with the following systems SAS, CDMS, EDC, SQL, VB, Java
• Knowledge of Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations;
• Ability to successfully work together with a team as well as independently;
• Demonstrate strong leadership ability, precision skills, organizational skills, prioritization skills, flexibility to change;
If you are interested in this position, please do send your CV with a cover note to Louise Beka
Our client covers a wide range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. In addition, they play a key part in the launching and development of some of the most important drugs.
As a Senior Programmer you will provide technical expertise for the conduct of clinical trials, act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to clinical systems, and/or analysis and reporting, and/or the applications/systems within eClinical technologies.
In addition, you will meet the requirements of a Programmer with a high degree of proficiency and autonomy; you will deliver best value with high quality service; coordinate projects and liaise with sponsors.
Your key responsibilities will include:
• Coordinate project start-up activities, creation of global programs, tracking spreadsheets, and required documentation;
• Assist in the production and QC of analysis plans, TLF, derived dataset specifications, programming specifications, and other process supporting documents;
• Use efficient programming techniques to produce and/or QC derived datasets tables, figures and data listings;
• Understand regulatory requirements concerning industry technical standards;
• Create standard macros and applications to improve the efficiency of the department
You have the following profile and experience:
• BA/BSc/MSc in Computer Sciences or equivalent;
• Minimum 4+ years experience as a SAS programmer;
• Fluent in English (spoken and written);
• Relevant Clinical Trial industry experience;
• Experience working with the following systems SAS, CDMS, EDC, SQL, VB, Java
• Knowledge of Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations;
• Ability to successfully work together with a team as well as independently;
• Demonstrate strong leadership ability, precision skills, organizational skills, prioritization skills, flexibility to change;
If you are interested in this position, please do send your CV with a cover note to Louise Beka
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