Opportunities have arisen for 2 new statisticians in Leeds, the opportunities are due to an expansion of our current team of 9 statisticians.
Please apply through the covance website.
http://www.covance.com, go to featured jobs and search Leeds.
Statistician I – LEEDS
We are currently recruiting for a Statistician I at our Leeds City centre site. As a Statistician I, you will responsible for providing a statistical analysis service and SAS programming support in terms of table production for all clinical studies as required. Other duties and responsibilities include:
- Preparation and review of Statistical Analysis Plans and Statistical Contributions, under the direction of senior Statistical staff.
- Statistical analysis of clinical trial data using basic methodology, under the direction of senior Statistical staff.
- Production of data tables and graphs to the required specification for clinical, pharmacokinetic and statistics reports.
- Generation of randomization schedules from provided specifications.
- May review the format of CRFs under the direction of senior Statistical staff.
- Perform sample size calculations as required.
- Maintain project administration files with regard to all documents produced by Biostatistics, including associated review, QC and project tracking information and internal and external communications.
- Provide statistical support to SAS Programmers.
- SAS programming and related activities for the presentation and analysis of clinical trial data.
- Scheduling of clinical statistical work to meet required deadlines. Ensuring that projects are completed in a timely and accurate manner.
- Liaison with internal and external clients, as required, with regards to the requirements for analysis, tables and graphs.
- Review of Clinical Study Reports.
About You
You will possess an MSc in Statistics and/ or with 1 or 2 years experience.
You will ideally have knowledge of SAS and have some experience of clinical research is preferred.
We Offer
Covance's ongoing success offers team members unsurpassed growth and career development opportunities.
At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.
There is no better time to join us!
Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.
Education/Qualifications Must hold an MSc in Statistics
Experience New MSc graduate, or with 1 or 2 years experience.
Must have knowledge of SAS and ideally have some experience of clinical research.
Leeds, UK
Leeds, United Kingdom
Senior Statistician – LEEDS
We are currently recruiting for a Senior Statistician at our Leeds City Centre site. As a Senior Statistician, you are responsible for providing a statistical analysis service for Covance studies, providing advice and assistance in the design of those studies. You will provide a contract statistics service to clients, including advice on design and appropriate statistical techniques. Other responsibilities and duties may include:
- Assume the role of Study Statistician for some studies, particularly non-standard / contract type studies.
- Development and review of Statistical Analysis Plans and Statistical Contributions, to include statistical methodology, statistical programming procedures, definition of derived variables, data handling rules and mock-ups.
- Statistical analysis of clinical trial data and related decision making.
- Responsible for statistical input to clinical study, pharmacokinetic and statistics reports.
- Maintain project administration files with regard to all documents produced by Biostatistics, including associated review, QC and project tracking information and internal and external communications.
- Review of protocols, providing a statistical advice service for internal and external clients.
- Scheduling of clinical statistical work to meet required deadlines. Ensuring that projects are completed in a timely and accurate manner.
- Perform QC of all efficacy and safety datasets and data displays.
- Review of Clinical Study Reports.
- Perform independent peer review of statistical deliverables.
- Provide statistical support to SAS Programmers.
About You
You will possess an MSc in Statistics with ideally 3 years or more relevant statistical and programming experience. Relevant experience within a CRO or Pharma industry would be advantageous.
We Offer
Covance's ongoing success offers team members unsurpassed growth and career development opportunities.
At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.
There is no better time to join us!
Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.
Education/Qualifications Must have an MSc in statistics, a pHd would be an advantage.
Experience Good SAS knowledge
2-3 years experience in a CRO or pharma company in clinical research
Leeds, UK
Leeds, United Kingdom
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