Hi All,
CK Clinical are recruiting for the following positions:
Contract Senior Statistician
UK based Pharmaceutical
£Competitive
* Application of expert statistical skills and thinking to optimally design a series of clinical studies in a specific therapeutic area or area of expertise (e.g. clinical pharmacology, discovery medicine, health economics).
* Application of expert statistical thinking to support risk assessment, decision-making processes (e.g. tollgate decisions, labelling), perform the statistical analysis of data from a series of studies and ensure appropriate interpretation of the results, provide support to the regulatory submissions including specification of overview documents and response to regulatory questions.
* Lead a study-specific or project-wide delivery team, or be the representative, as agreed with management and the project team.
* Negotiation of time frames for the completion of tasks.
* Delivery of the tasks as agreed and present results effectively.
* Management of statistical work contracted out to a CRO or research collaborator.
Interested applicants should hold a BS/BSc in Statistics or related field with experience as a statistician in the health care environment or relevant statistical applications
MS/MSc in Statistics or Medical Statistics is desirable.
Contract Statistician
Switzerland, EU
£Excellent
* Being responsible for all statistical tasks of the assigned clinical studies e.g. clinical trial design/planning, analysis plan, reporting activities, support to publications, and any statistical consultation during the running phase.
* Tracking clinical trial / allocated project activities and milestones.
* Interacting with the Company's Methodology group as appropriate.
* Ensuring timelines and adequate quality of all Biostatistics and Statistical Reporting deliverables for the assigned trials and project task.
* Following processes and adhere to the company's project specific standards as well as Health Authority requirements (SOPs, Master Analysis Plan, full development project specifications, and regulatory guidelines).
* Establishing and maintaining sound working relationships and effective communication within the clinical trial team.
Interested applicants will hold an MSc in Statistics (or equivalent degree) with proven relevant experience within the Pharmaceutical arena. You will also have knowledge of statistical software packages; strong knowledge of SAS and the drug development process together with a high degree of autonomy in performing assigned duties.
Experience in statistical modelling and knowledge of Bayesian design & techniques together with Knowledge of S+ is desirable.
Contract SAS Programmer
UK based Pharmaceutical
£Negotiable
* Providing statistical programming and validation support for analysis datasets, statistical tables, figures, listings, patient profiles, SAS transport files, Integrated Summaries of Safety (ISS), electronic submissions, related clinical trials, and other internal/external requests.
* Working with external vendors in order to develop or monitor the content and structure of SAS datasets, when necessary.
* Contributing to the overall efficiency and best practice running of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment.
* Developing and maintaining SOPs, SWPs and other related technical documents, providing input to the Database and CRF Development and providing feedback to Data Management.
* Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents and determining and researching SAS software upgrades and related system maintenance issues.
* Providing Statistical Support for the Statistician responsible for the study.
Interested applicants will have proven experience in SAS Programming within Phases I-IV clinical trials in a Pharmaceutical/CRO environment. You will also have a working knowledge of CDISC (SDTM and ADaM) together with experience using SAS-Base, MACRO, STAT, GRAPH, and ACCESS within Unix and Windows operating systems.
SAS Programmer (Permanent)
UK based Bio-Pharmaceutical
£Dependant upon Experience
* Provides clinical programming support to projects; failure can cause delays for organization.
* Interacts with Biostatisticians, Data Management, Programmers, Clinical Development staff and management as directed by the Project Lead Programmer.
* Keeps the Project Lead Programmer apprised of status, accomplishments and issues.
* Develops analysis datasets, Tables, Listings & Graphs under the direction of the Project Lead Programmer.
* Validates moderately complex deliverables when needed.
* Responds to simple ad-hoc requests.
* Providing support role on one or more protocols and learning industry.
Interested applicants will hold a BSc (or equivalent) in Mathematics, Statistics or Life Sciences and proven industrial experience as a SAS Programmer within the Pharmaceutical field. You will also be proficient in SAS/BASE, SAS/STAT and SAS/GRAPH.
As always, we would be delighted to hear from you, if you are interested please contact Priya Mukherjee on 01438 870028 or email an updated CV to [log in to unmask]
CK Clinical are still giving away £75 Amazon vouchers as part of our referral scheme, so kindly forward this email to friends or fellow colleagues.
I look forward to hearing from you,
Best wishes,
Priya
Priya Mukherjee BSc (Hons) MRec CertRP
Senior Consultant
CK Clinical Limited
9 High Street
Stevenage Old Town
Hertfordshire
SG1 3BG
Direct Dial: 01438 870028
Tel: 01438 743047
Fax: 01438 723800
You may leave the list at any time by sending the command
SIGNOFF allstat
to [log in to unmask], leaving the subject line blank.
|