Job Title: Contract Study Statistician or Programmer (Ref.10388)
Location: UK South - or HOME BASED IF YOUM HAVE BROADBAND
Benefits: Our Client provides a comprehensive remuneration and benefits
package, work-life balance initiatives and social events. Viewed together,
these benefits present significant financial, personal and professional
growth opportunities. Further information is available on application.
Job Role: You will be primarily responsible for
· Statistical/programming input to the reporting of clinical studies
· Ensure that activities and processes performed are conducted
according to company requirements
· Working closely with other team members
To include -
· Acting as a representative Statistician/Programmer on study teams,
managing your time so as to provide timely input
· SAS programming to support the Statistical reporting, including
production of listing, tables and figures, for Phase II and Phase III
clinical studies.
· Programming/performing statistical analyses of data
· Interpreting analysis results, ensuring validity of conclusions
· Performing quality control review of study results
· Acting as a statistical/programming contact within the company
· Interacting with Data Management personnel to ensure that data are
in usable format; performing appropriate diagnostics prior to database
locking
· Interacting with report writers in the production of integrated
clinical reports and other documents containing information from clinical
study databases
· Exploring data for product profiling, hypothesis generation, new
research topics and publications
· Inputting into the development of departmental processes,
including standard working practices and operating procedures
Minimum Requirements:
· A relevant Bachelors or Masters degree, with 3+ years of relevant
pharmaceutical experience.
· Good knowledge of applicable regulatory requirements and
guidelines, e.g. ICH Guidelines.
· Proficient in the use of computers using the Windows Operating
System and Microsoft Office products. .
· A high level of computer proficiency, including SAS programming
ability, is required.
· Have a good understanding of clinical data, including data quality
issues.
· This position holder must be able to work without close
supervision. Well-developed time management skills are important.
· Able to work in a fast-paced, team-oriented environment.
· Possess excellent interpersonal and communication skills (written
and verbal).
· Strong attention to detail with a view to bring studies to a
quality conclusion.
· Flexible, positive, creative thinker, good communicator.
Unique Benefits: This is an excellent window for a statistician with
pharma experience to join a dynamic innovative company in Cambridgeshire.
Keywords: Statistician, Statistics, Statistical Programming, Statistical
Analysis, SAS, Statistical Analyst, Statistical Programmer, Clinical Study
Trials, Clinical Trials
Fforde specialises in the supply of staff within the Pharmaceutical, CRO
and Biotechnology sectors.
www.fforde-management.com
Email your CV to: [log in to unmask]
Speak to: David on 01273 722366
Or write to us at Curtis House, 34 Third Avenue, Hove BN3 2PD
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