Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Senior SAS Programmer - Basel - Pharmaceuticals
Eingestellt von Darwin Recruitment
Gesuchte Skills: Support, Design
Projektbeschreibung
SENIOR SAS PROGRAMMER - BASEL - PHARMACEUTICALS
LEADING PHARMACEUTICAL COMPANY IN BASEL ARE CURRENTLY SEEKING A SAS PROGRAMMER TO JOIN AN EVOLVING TEAM OF SPECIALISTS IN THEIR ONCOLOGY DEPARTMENT.
JOB FUNCTIONS:
- COORDINATE PROGRAMMING ACTIVITIES ACROSS SEVERAL TRIALS WITH A GIVEN COMPOUND INCLUDING PUBLICATION AND REGULATORY SUBMISSION ACTIVITIES.
- DEVELOP PROGRAMMING SPECIFICATIONS FOR ANALYSIS DATASETS, POOLED DATASETS AND DELIVERABLES IN CONSULTATION WITH THE STATISTICIAN.
- DEVELOP AND COMPLY WITH PROJECT/STUDY PROGRAMMING STANDARDS AND SPECIFICATIONS FOLLOWING INTERNAL GUIDELINES
- PROGRAM ACCORDING TO SPECIFICATIONS, ANALYSIS DATASETS, POOLED DATASETS, LISTINGS, AND FIGURES FOR CLINICAL TRIALS AND SUBMISSION ACTIVITIES
- SUPPORT QUALITY CONTROL AND QUALITY AUDIT OF DELIVERABLES
- PROVIDE INPUT AS REQUIRED AT ALL MEETINGS, DISCUSSIONS AND ACTIVITIES COVERING ASPECTS OF STATISTICAL REPORTING ON TRIAL LEVEL ACTIVITIES
- TRACK CLINICAL TRIAL MILESTONES FOR STATISTICAL REPORTING DELIVERABLES.
- MAINTAIN RECORDS FOR ALL ASSIGNED PROJECTS AND ARCHIVING OF TRIAL/PROJECT ANALYSIS AND ASSOCIATED DOCUMENTATION.
- MAINTAIN EFFICIENT INTERFACES WITH INTERNAL AND EXTERNAL CUSTOMERS AND COMMUNICATE EFFECTIVELY ACROSS LINE FUNCTIONS.
KEY SKILLS:
- EXPERIENCE USING SAS IN THE ANALYSIS AND THE REPORTING OF PHARMACEUTICAL DATA
- WORKING KNOWLEDGE OF DATABASE DESIGN/STRUCTURES
- EXPERTISE WITH SAS (INCLUDING SAS MACRO LANGUAGE)
PLEASE SEND CV FOR IMMEDIATE CONSIDERATION.
LEADING PHARMACEUTICAL COMPANY IN BASEL ARE CURRENTLY SEEKING A SAS PROGRAMMER TO JOIN AN EVOLVING TEAM OF SPECIALISTS IN THEIR ONCOLOGY DEPARTMENT.
JOB FUNCTIONS:
- COORDINATE PROGRAMMING ACTIVITIES ACROSS SEVERAL TRIALS WITH A GIVEN COMPOUND INCLUDING PUBLICATION AND REGULATORY SUBMISSION ACTIVITIES.
- DEVELOP PROGRAMMING SPECIFICATIONS FOR ANALYSIS DATASETS, POOLED DATASETS AND DELIVERABLES IN CONSULTATION WITH THE STATISTICIAN.
- DEVELOP AND COMPLY WITH PROJECT/STUDY PROGRAMMING STANDARDS AND SPECIFICATIONS FOLLOWING INTERNAL GUIDELINES
- PROGRAM ACCORDING TO SPECIFICATIONS, ANALYSIS DATASETS, POOLED DATASETS, LISTINGS, AND FIGURES FOR CLINICAL TRIALS AND SUBMISSION ACTIVITIES
- SUPPORT QUALITY CONTROL AND QUALITY AUDIT OF DELIVERABLES
- PROVIDE INPUT AS REQUIRED AT ALL MEETINGS, DISCUSSIONS AND ACTIVITIES COVERING ASPECTS OF STATISTICAL REPORTING ON TRIAL LEVEL ACTIVITIES
- TRACK CLINICAL TRIAL MILESTONES FOR STATISTICAL REPORTING DELIVERABLES.
- MAINTAIN RECORDS FOR ALL ASSIGNED PROJECTS AND ARCHIVING OF TRIAL/PROJECT ANALYSIS AND ASSOCIATED DOCUMENTATION.
- MAINTAIN EFFICIENT INTERFACES WITH INTERNAL AND EXTERNAL CUSTOMERS AND COMMUNICATE EFFECTIVELY ACROSS LINE FUNCTIONS.
KEY SKILLS:
- EXPERIENCE USING SAS IN THE ANALYSIS AND THE REPORTING OF PHARMACEUTICAL DATA
- WORKING KNOWLEDGE OF DATABASE DESIGN/STRUCTURES
- EXPERTISE WITH SAS (INCLUDING SAS MACRO LANGUAGE)
PLEASE SEND CV FOR IMMEDIATE CONSIDERATION.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Medien/Design, Sonstiges