Dear Allstat,
Please find the latest Permanent position.
A pharmaceutical company in Switzerland, which just made the decision lately
to push a further growth in the next few months within clinical trial
development.
This gives new permanent employees a good chance to grow with the firm and
bring career opportunities in the future.
This is definitely an exciting and challenging position with a friendly and
very international environment.
This position provides statistical input into Pharmacological Phase and
Phase I clinical trial development, performs the analysis of clinical trial
data, and provides statistical input into the reporting of clinical trial
results.
The Role:
* Provides statistical input into protocol/CRF development in the
therapeutic areas metabolism, reproductive health and
autoimmune/inflammatory of the client (e.g., trial design, sample size
estimation, randomization, statistical methods for protocols, query checks
for clinical trial data).
* Write detailed statistical analysis plans for clinical trials as
well as for integrated summaries of efficacy and safety.
* Analyse clinical trial data producing accurate results representing
the outcome of the trial.
* Validate statistical output.
* Accurately interpret and clearly communicate statistical results and
concepts to non-statisticians.
* Co-author final integrated reports of clinical trial data writing
thorough and clear statistical methods sections and producing the
statistical appendix for the reports.
* Provide statistical output as required for manuscripts and ensure
that the results are accurately interpreted in the publications.
* Provide input into statistical SOPs and general standardization
efforts within the department (e.g. statistical methodology standards,
standard data presentations).
* Participate in interactions with regulatory agencies as required.
* Collaborate effectively with members of clinical trial
implementation teams and with Biometrics colleagues.
Qualifications / Experience needed
* Fluency in English.
* Ph.D. in Statistics or Biostatistics with at least 2 years
pharmaceutical/ biotechnology experience OR a Masters Degree in Statistics
Biostatistics with at least 5 years pharmaceutical/biotechnology experience.
Professional Skills and Experience
* Experience in metabolism / reproductive health / autoimmune,
inflammatory preferred.
* Working SAS knowledge and proficient in SAS statistical procedures.
* Knowledge of ICH statistical regulatory requirements.
Personal Qualifications
* Interpersonal skills, initiative, creativity.
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 mathew.hogan <mailto:[log in to unmask]>
@1st-pharmapeople.com
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]
<http://www.1st-pharmapeople.com/> 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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