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Statistician
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Support
Projektbeschreibung
Harvey Nash is looking for a Statistician for a 6 month project in Switzerland.
The role is for a candidate who is 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.
You are responsible for
- Coordinating study tasks with other statisticians and statistical programmers
- Ensuring timeliness and adequate quality of all statistical deliverables
- Following processes and adhere to clients and project standards as well as Health Authority requirements
Requirements
- At least 5 years experience in pharmaceutical development and clinical research
- Minimum MSc in statistics
- 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 all tasks of a CP Statistician. Proven knowledge in Statistics and its applications to clinical trials and their PK/PD parts
- Experience in Oncology
- Proven knowledge in Statistics and its applications to clinical trials and their PK/PD parts.
- Candidates with experience in clinpharm are preferred.
- Fluent in English, good oral and written communication skills
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred)
The role is for a candidate who is 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.
You are responsible for
- Coordinating study tasks with other statisticians and statistical programmers
- Ensuring timeliness and adequate quality of all statistical deliverables
- Following processes and adhere to clients and project standards as well as Health Authority requirements
Requirements
- At least 5 years experience in pharmaceutical development and clinical research
- Minimum MSc in statistics
- 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 all tasks of a CP Statistician. Proven knowledge in Statistics and its applications to clinical trials and their PK/PD parts
- Experience in Oncology
- Proven knowledge in Statistics and its applications to clinical trials and their PK/PD parts.
- Candidates with experience in clinpharm are preferred.
- Fluent in English, good oral and written communication skills
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred)
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges