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Biostatistician 8878KS
Eingestellt von ITech Consult
Gesuchte Skills: Support, Consultant
Projektbeschreibung
Biostatistician m/f 04.12.2012
Reference Nr.:
8878KS
Branch:
Medical
Location:
Basel
Start:
ASAP
Duration:
6 months
Introduktion:
For our client we are searching a Biostatistician to start as soon as possible.
RESPONSIBILITIES:
Responsible for all statistical tasks for assigned clinical trials in the Oncology therapeutic area. This includes: protocol writing, analysis planning and reporting, exploratory analyses, publication support, and statistical consultation. Coordinate study tasks with other statisticians and statistical programmers. Ensure timeliness and adequate quality of all statistical deliverables. Follow processes and adhere to project standards as well as Health Authority requirements.
KEY JOB SKILLS:
Minimum MSc in statistics. At least 5 years experience in pharmaceutical development and clinical research. Strong statistical skills and knowledge of clinical trials methodology: experience with protocol development, analysis planning and reporting of clinical trials. Knowledge of SAS. Experience in Oncology. Good team player. High degree of autonomy in performing assigned duties. Able to establish personal relationships with personnel from other line functions. Experience with intercultural teams
Languages
Fluent in English, good oral and written communication skills
Kathrin Schrickel
Recruitment Consultant
ITECH CONSULT AG
Reference Nr.:
8878KS
Branch:
Medical
Location:
Basel
Start:
ASAP
Duration:
6 months
Introduktion:
For our client we are searching a Biostatistician to start as soon as possible.
RESPONSIBILITIES:
Responsible for all statistical tasks for assigned clinical trials in the Oncology therapeutic area. This includes: protocol writing, analysis planning and reporting, exploratory analyses, publication support, and statistical consultation. Coordinate study tasks with other statisticians and statistical programmers. Ensure timeliness and adequate quality of all statistical deliverables. Follow processes and adhere to project standards as well as Health Authority requirements.
KEY JOB SKILLS:
Minimum MSc in statistics. At least 5 years experience in pharmaceutical development and clinical research. Strong statistical skills and knowledge of clinical trials methodology: experience with protocol development, analysis planning and reporting of clinical trials. Knowledge of SAS. Experience in Oncology. Good team player. High degree of autonomy in performing assigned duties. Able to establish personal relationships with personnel from other line functions. Experience with intercultural teams
Languages
Fluent in English, good oral and written communication skills
Kathrin Schrickel
Recruitment Consultant
ITECH CONSULT AG
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Organisation/Management, Sonstiges