Clinical Statistician in Yorkshire
- Recruiter
- CK GROUP
- Location
- Lincolnshire
- Salary
- ,
- Posted
- 26 Jun 2019
- Closes
- 18 Jul 2019
- Sectors
- Scientific & Pharmaceutical
- Contract Type
- Permanent
- Hours
- Full Time
Stephanie Maccioni is recruiting for a Clinical Statistician to join a well respected Consumer Health Company at their site based in Yorkshire on a permanent basis.
This role supports Medical Affairs & Clinical Research to meet business objectives through optimal insight into products from available data, sound oversight of clinical study activities and the generation of evidence.
Principal Responsibilities will include:
- Author or review the statistical considerations in Protocols.
- Review and approve CRFs, Data Validation Plans, and Statistical Analysis Plans.
- Perform data reviews prior to database lock.
- Perform QC of key top-line outputs using the raw database and additional analysis as required.
- Review Clinical Study Reports.
- Ensure accurate interpretation of statistical results from clinical studies in the Clinical Study Reports and Publications as well as at top-line results presentations.
- Manage and adhere to agreed timelines for studies.
Qualifications/Experience Requirements:
- Experience working as a Statistician in pharmaceutical/consumer healthcare/cosmetic industry or at a CRO or clinical vendor.
- Good knowledge of SAS Programming, statistical methods and statistical concepts in clinical studies.
- Good understanding of the statistical processes, standards and software used in clinical studies.
Full job description available upon request.
Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.
CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 45492 in all correspondence.
This role supports Medical Affairs & Clinical Research to meet business objectives through optimal insight into products from available data, sound oversight of clinical study activities and the generation of evidence.
Principal Responsibilities will include:
- Author or review the statistical considerations in Protocols.
- Review and approve CRFs, Data Validation Plans, and Statistical Analysis Plans.
- Perform data reviews prior to database lock.
- Perform QC of key top-line outputs using the raw database and additional analysis as required.
- Review Clinical Study Reports.
- Ensure accurate interpretation of statistical results from clinical studies in the Clinical Study Reports and Publications as well as at top-line results presentations.
- Manage and adhere to agreed timelines for studies.
Qualifications/Experience Requirements:
- Experience working as a Statistician in pharmaceutical/consumer healthcare/cosmetic industry or at a CRO or clinical vendor.
- Good knowledge of SAS Programming, statistical methods and statistical concepts in clinical studies.
- Good understanding of the statistical processes, standards and software used in clinical studies.
Full job description available upon request.
Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.
CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 45492 in all correspondence.