Principal Statistician
Syneos Health · Biopharmaceutical Services
- Work arrangement: hybrid
- Employment type: Full Time
- Seniority: senior
- Posted:
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Job description
Position:
Principal Statistician - Early Phase - Fully home based (located in Europe)
Company:
Syneos Health
Location:
Europe or Poland
Employment type:
Full Time
Work Arrangement:
Remote
Short Summary:
Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Responsibilities:
- Serves as a statistical department resource, mentors biostatisticians on job skills, and oversees or develops training plans or materials for Biostatistics associates.
- Conducts training sessions, or otherwise trains new hires and enhances the skills of existing personnel.
- Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high-quality work.
- Provides independent review of project work produced by other biostatisticians in the department.
- Prepares or oversees the preparation of Statistical Analysis Plans (SAPs), including development of well-presented mock-up displays for tables, listings, and figures.
- Collaborates with sponsors, if required.
- May be responsible as Lead Biostatistician for the statistical aspects of the protocol, generation of randomization schedule, and input to the clinical study report.
- Creates or reviews programming specifications for analysis datasets, tables, listings, and figures.
- Reviews SAS/R annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met.
- Implements company objectives, and creates alternative solutions to address business and operational challenges.
- Monitors progress on study activities against agreed-upon milestones and ensures the study timelines for project deliverables are met.
Requirement:
- Graduate degree in biostatistics or related discipline.
- Extensive experience in clinical trials or an equivalent combination of education and experience, demonstrated by the ability to lead multiple projects and programs of studies.
- Proficiency in R programming.
- Excellent written and verbal communication skills.
- Ability to read, write, speak, and understand English.
Benefits:
- Passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- Committed to building an inclusive culture – where you can authentically be yourself.
Principal Statistician - Early Phase - Fully home based (located in Europe)
Company:
Syneos Health
Location:
Europe or Poland
Employment type:
Full Time
Work Arrangement:
Remote
Short Summary:
Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Responsibilities:
- Serves as a statistical department resource, mentors biostatisticians on job skills, and oversees or develops training plans or materials for Biostatistics associates.
- Conducts training sessions, or otherwise trains new hires and enhances the skills of existing personnel.
- Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high-quality work.
- Provides independent review of project work produced by other biostatisticians in the department.
- Prepares or oversees the preparation of Statistical Analysis Plans (SAPs), including development of well-presented mock-up displays for tables, listings, and figures.
- Collaborates with sponsors, if required.
- May be responsible as Lead Biostatistician for the statistical aspects of the protocol, generation of randomization schedule, and input to the clinical study report.
- Creates or reviews programming specifications for analysis datasets, tables, listings, and figures.
- Reviews SAS/R annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met.
- Implements company objectives, and creates alternative solutions to address business and operational challenges.
- Monitors progress on study activities against agreed-upon milestones and ensures the study timelines for project deliverables are met.
Requirement:
- Graduate degree in biostatistics or related discipline.
- Extensive experience in clinical trials or an equivalent combination of education and experience, demonstrated by the ability to lead multiple projects and programs of studies.
- Proficiency in R programming.
- Excellent written and verbal communication skills.
- Ability to read, write, speak, and understand English.
Benefits:
- Passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- Committed to building an inclusive culture – where you can authentically be yourself.
Skills
- r
Languages
EN
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