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Clinical Statistician
Eingestellt von Harvey Nash IT Recruitment Belgium
Gesuchte Skills: Design, Support
Projektbeschreibung
Job description
Within the biostatistics and Data management team of our customer, biostatisticians provide statistical expertise and support in the development of prophylactic or therapeutic vaccines. Amongst the 90 statisticians part of an international team and devoted to the discovery and development of vaccines, an expanding team of about 10 statistical programmers are providing statistical expertise to the cancer immunotherapeutics clinical development. Currently two Phase III studies are ongoing in non-small cell lung cancer and melanoma and earning we are creative, always We are a growing team sharing from each other, looking for new and better ways to do our job. We focus on performance but recognize there is no achievement without integrity.
What you'll do
You will participate in the cancer immunotherapeutics development plan (trial designs sample sizes, interim analysis, etc.) in collaboration with clinical development managers and safety physicians, In particular, and scientific input into clinical development planning
Be responsible for the statistical designs of clinical trials, creating statistical sections or study synopses and protocols
Input in study set up (case report forms, database, randomization)
Explore new statistical approaches and methodologies through innovative and creative thinking
Interact with regulatory authorities
Propose and evaluate the perform ance of statistical methods in order to prepare statistical analysis plans
Perform statistical analysis, run simulations and discuss with internal and external expert
Support scientific writers and clinicians to correctly interpret the statistical results and align them with the clinical report conclusions
Write the statistical sections of clinical study reports, statistical publications and prepare materials for publications and create statistical text for clinical study communications
Profile
At least 5-7 years of experience in Statistics
Good knowledge of statistical approaches applied in cancer clinical trials with a focus on survival anal techniques
Techniques Comprehensive understanding of applied statistical principles and modelling in the design and analysis of clinical trials
Experience in statistical or clinical trial methodology research and presentations on statistical methods, clinical trial design and analysis.
Required Skills
Ability to easily communicate with different functions: clinicians, scientists, data managers, scientific writers commercials, etc. in an international, multi-cultural environment
Compliance with internal Standard Operating Procedures and regulatory guidelines
Proficency in SAS knowledge or other statistical software is an asset
Fluent in French and English
Within the biostatistics and Data management team of our customer, biostatisticians provide statistical expertise and support in the development of prophylactic or therapeutic vaccines. Amongst the 90 statisticians part of an international team and devoted to the discovery and development of vaccines, an expanding team of about 10 statistical programmers are providing statistical expertise to the cancer immunotherapeutics clinical development. Currently two Phase III studies are ongoing in non-small cell lung cancer and melanoma and earning we are creative, always We are a growing team sharing from each other, looking for new and better ways to do our job. We focus on performance but recognize there is no achievement without integrity.
What you'll do
You will participate in the cancer immunotherapeutics development plan (trial designs sample sizes, interim analysis, etc.) in collaboration with clinical development managers and safety physicians, In particular, and scientific input into clinical development planning
Be responsible for the statistical designs of clinical trials, creating statistical sections or study synopses and protocols
Input in study set up (case report forms, database, randomization)
Explore new statistical approaches and methodologies through innovative and creative thinking
Interact with regulatory authorities
Propose and evaluate the perform ance of statistical methods in order to prepare statistical analysis plans
Perform statistical analysis, run simulations and discuss with internal and external expert
Support scientific writers and clinicians to correctly interpret the statistical results and align them with the clinical report conclusions
Write the statistical sections of clinical study reports, statistical publications and prepare materials for publications and create statistical text for clinical study communications
Profile
At least 5-7 years of experience in Statistics
Good knowledge of statistical approaches applied in cancer clinical trials with a focus on survival anal techniques
Techniques Comprehensive understanding of applied statistical principles and modelling in the design and analysis of clinical trials
Experience in statistical or clinical trial methodology research and presentations on statistical methods, clinical trial design and analysis.
Required Skills
Ability to easily communicate with different functions: clinicians, scientists, data managers, scientific writers commercials, etc. in an international, multi-cultural environment
Compliance with internal Standard Operating Procedures and regulatory guidelines
Proficency in SAS knowledge or other statistical software is an asset
Fluent in French and English
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Sonstiges