Dear Allstat,

 
Job Title:           Senior Statistical Programmer

Department:          Biostatistics and Statistical Programming


Core Responsibilities:

*     Statistical programming for both production and QC of derived
datasets, data 	listings, data summaries, figures and statistical appendices
for global 		Phase I-IV trials.

*     Creation of study specifications for analysis datasets and pooled
datasets for 	phase I-IV clinical trials.

*     Responsible for the quality and timeliness of statistical programming
deliverables.

*     As Lead Programmer, to be primarily responsible for all statistical
programming activities on allocated studies including planning and
coordination of 	activities for assigned statistical programming team
members.

Principal Accountabilities:

*     Program analysis datasets, pooled datasets, listings, summaries,
figures and 	tables for phase I-IV clinical trials and for overall
summaries of safety and 	efficacy to my client and/or client
specifications.

*     Production of study specifications for analysis datasets and pooled
datasets 	for 	phase I-IV clinical trials.

*     Provide input as appropriate into specifications for data listings,
data 	summaries/tables and figures for phase I-IV clinical trials, and for
overall 	summaries of safety and efficacy, to ensure adherence to the
standards of my 	client and/or the client.

*     Provide quality control for the above deliverables.

*     Produce SAS programs written to a standard as defined by my client
and/or client 	good programming practice requirements.

*     Clearly document all work ensuring that program and project
documentation are 	maintained to a high standard and on an ongoing
basis.

*     Provide programming input into CRF(s) and data management plan(s) to
ensure that 	these documents are consistent and adhere to the standards
of my client and/or the 	client.



*     Provide input from a statistical programming perspective to the
statistical 	analysis plan, the QC plan and project convention documents.

*     Provide input into specifications of data structures and databases to
ensure 	adherence to my client and/or client standards.

*     Adhere to pre-defined project/study standards and specifications.

*     Input into estimation of task durations for programming deliverables.

*     Maintain efficient interfaces with internal and external customers in
consultation 	with my client management.

*     Perform role of Lead Programmer on selected studies.

*     Provide transfer of SAS derived datasets, outputs and programs (as
appropriate) 	from my client to Client.

*     Ensure timely and accurate entry of relevant study information occurs
in MIS.

*     Ensure project and resource tracking sheets are accurate and updated
as required.

*     Maintain up-to-date knowledge of new developments/functionality of SAS
as new 	versions are released.

*     Actively participate at meetings, discussions and activities covering
statistical 	programming aspects for assigned trials.

*     Provide input to departmental processes and procedures and take part
in/lead 	process initiatives as required by management.

*     Act as a SAS programming consultant to clients and internal customers
for 	projects.

*     Induct, coach, supervise and train programmers as appropriate on
technical, trial 	and project level processes.

*     Conduct departmental training workshops or presentations as required.

*     Provide input to the appraisal process when required.

*     Provide input into recruitment process including interviewing.

*     Participate in, and support business development, e.g. bid defence
meetings etc.

*     Ensure timesheets are accurate and updated on a weekly basis in MIS.
Essential 	Work Experience and Qualifications

*     Minimum of BSc/BA or equivalent in computer science, mathematics,
statistics, life 	sciences or related field(s).

*     Excellent SAS programming skills (BASE, MACRO, GRAPH).

*     Knowledge and experience in database design and structures.

*     Minimum of 4 years experience in programming in a clinical trials
environment.

*     Knowledge of clinical trial practices, procedures and methodologies.

*     Good knowledge of statistical principals underlying clinical trials.


My client Core Values:

All My client employees are required to exhibit and demonstrate the my
client 'Core values'.

*         Client focus. Satisfaction and Solutions

*         Dependability. Competence and Quality

*         Trustworthy. Open and Honest.

*         Innovative. Approaches and Technology

*         Winners. Win-Win


Attributes Include.

*         Good organizational/time management skills.

*         A good understanding of resourcing and budgeting; business
awareness.

*         Excellent interpersonal and communication skills and the ability
to operate 	    effectively in a global working environment.

*         Work calmly under pressure and meet agreed deadlines.

*         Professional, positive and enthusiastic attitude.

*         A good understanding of medical terminology, clinical trial
methodology and 	    ICH/GCP.

*         An excellent investigative and meticulous approach to all
activities and 	    tasks.

*         Transparent approach, clear and precise.

*         Team player.

*         The ability to delegate tasks appropriately.


I also have a variety of other Biometric specific vacancies available in the
UK and throughout Europe. 

Inclusive of SAS Programming, Statistical, Data Management functions, please
call me for further details....

If you would like to discuss this role in greater detail or your application
/ suitability to this or further roles, please call me or e-mail me in
confidence. If you are not available or suited to this position, please feel
free to pass my details on.

For a confidential consultation call Mathew Hogan on 0044 (0) 207 255 6665
or email your CV to [log in to unmask]

Regards

 
Mathew Hogan
Senior Consultant
Pharmaceutical, Biometrics & CRO Division

1st Pharma People
A Division of 1st-IT People
Tel: +44 (0) 207 255 6665
Fax: +44 (0) 207 255 6656
mailto:[log in to unmask]
<mailto:[log in to unmask]> 
www.1st-pharmapeople.com <http://www.1st-pharmapeople.com/> 
 
PLEASE NOTE: As of 31st May 2005 our office address will change to; 1st IT
People, 3rd Floor, Woolverstone House, 61-62 Berners Street, London. W1T
3NJ. As a result of this, we do have a new telephone number of 0207 255
6665. Please note our previous phone number will still work.

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