Dear Statisticians,
We currently have career opportunities in Berkshire (permanent) and Scotland or Cambridge (Permanent) for Statisticians with various working experience within the Pharmaceutical Industry. Please see below :-
Career Opportunities For Statisticians/Senior Statisticians based In Berkshire
Duties and Responsibilities :
Track study progress for the relevant milestones and produce monitoring and evaluation reports for internal and client information using MS-Access Tracking System.
Where applicable supply statistical input to all protocols, CRF's, final reports and other documentation for assigned projects.
Where applicable for each assigned study, produce a statistical analysis plan.
For all assigned projects, oversee or perform the statistical analysis.
Assist in the management, supervision, professional development and training, evaluation and where applicable, recruitment of new statistical staff.
Perform and /or oversee the QC of the statistical output.
The requirements :
A BSc degree in a statistical or related mathematical science.
A minimum of 3 years clinical experience for the Senior role, with the ability to lead a project and be responsible for at least one other statistician.
Alternatively, equivalent previous experience in a clinical development or related statistical environment.
Good clinical knowledge with an understanding of medical terminology.
Understanding or previous experience with statistical software packages, preferably SAS.
Computer literacy with working knowledge of PC's, Windows and Microsoft Office applications.
Understanding of the principles of project management.
Good oral and written communication and coordination skills with the ability to conduct meetings.
Career Opportunity For Statistics Group Leader based In Berkshire
Duties and Responsibilities :
Assume responsibility for resourcing, co-ordinating and/or performing the accurate completion of the statistical sections, including reporting, for any assigned projects to the clients required quality standards and timelines.
Responsible for ensuring that there are adequate resources at all times to perform any statistical and programming tasks that are necessary through the recruitment of all statistical staff, the coordination and scheduling of statistical tasks through liaison with data managers, report writers and Head of Biometrics.
Responsible for the professional development and training and evaluation through annual appraisal of all statistical staff.
Track study progress for the relevant milestones and produce monitoring and evaluation reports for internal and client information using MS-Access Tracking System.
Where applicable supply statistical and/or programming input to all protocols, CRF's, final reports and other documentation for assigned projects.
Where applicable for each assigned study, produce a statistical analysis plan.
Perform and /or oversee the QC of the statistical output.
The requirements :
A BSc degree in a statistical or related mathematical science.
Previous experience of personnel management.
Alternatively, equivalent previous experience in a clinical development environment.
Good clinical knowledge with an understanding of medical terminology.
Understanding or previous experience with statistical software packages, preferably SAS.
Computer literacy with working knowledge of PC's, Windows and Microsoft Office applications.
Understanding of the principles of project management.
Good oral and written communication and coordination skills with the ability to conduct meetings.
Career Opportunity For Biometrics SAS Programmer based In Berkshire
Duties and Responsibilities :
Assume responsibility for resourcing, co-ordinating and/or performing the accurate completion of the programming sections of any of the groups assigned projects to the clients required quality standards and timelines.
Track study progress for the relevant milestones and produce monitoring and evaluation reports for internal and client information using MS-Access Tracking System.
Where applicable supply input to all protocols, CRF's, final reports and other documentation for assigned projects.
Where applicable for each assigned study review the validation plan and analysis plan.
Create, test and document all SAS programmes as required.
Assist in the management, supervision, professional development and training, evaluation and where applicable, recruitment of new programming staff.
Be instrumental in the provision of training to the Biometrics Dept. with respect to SAS programming.
Perform and /or oversee the QC of SAS programmes.
The requirements :
A BSc degree in a biomedical or related life science.
Alternatively, equivalent previous experience in a clinical development or related statistical environment.
Previous experience of personnel management.
Good clinical knowledge with an understanding of medical terminology.
Understanding or previous experience of Clintrial and programming in SAS - SAS Base, AF, FS - edit, PROCs etc.
Computer literacy with working knowledge of PC's, Windows and Microsoft Office applications.
Understanding of the principles of project management.
Good oral and written communication and coordination skills with the ability to conduct meetings and training sessions.
Career Opportunity For Statistician based In Cambridge or Scotland
Duties and Responsibilities :
To draft statistical analysis sections of protocols and analysis plans.
To draft statistical reports or statistics contributions to the integrated reports.
To carry out quality control of statistics work.
To liaise with members of Biostatistics team.
Review Data Management manuals.
The requirements :
Degree level, or equivalent, including a minimum of 1.5 years equivalent courses in statistics.
No experience necessary.
Sound knowledge of statistical methodology, good communication and interpersonal skills.
Career Opportunity For Statisticians/Senior Statisticians based In Cambridge
Duties and Responsibilities :
Provide statistical input on study design and for the analysis and reporting of phase I-III trials, including interpretation of data, writing the relevant sections of protocols and reports.
The requirements :
MSc in Statistics with at least 2 years (4-5 years for the senior role) relevant experience in drug development either in industry or with a CRO.
SAS programming experience.
Good communication skills.
Ability to work effectively as part of a multi-disciplinary team.
For the senior role you will be expected to make a significant contribution to the creation of a brand new biometric function, including the establishment of departmental working practices, reporting standards and SOP's. Line Management experience will be considered valuable.
To apply for these positions please send your CV by return of e mail, taking care to reply only to sender, or call on the number below for an informal chat.
Thanks and Regards
Zoe Beardmore
Contract Personnel Executive
Chiltern International Limited
Wellington House
20 Queensmere
Slough SL1 1DB
United Kingdom
Direct Line: +44 (0) 1753 216651
Fax: +44 (0) 1753 511116
Website www.chiltern.com
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