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ALLSTAT  February 2011

ALLSTAT February 2011

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Subject:

*** Hays Pharma - Senior Biostatistician - Leading Pharmaceutical company - France ***

From:

Laura Christie <[log in to unmask]>

Reply-To:

Laura Christie <[log in to unmask]>

Date:

Thu, 24 Feb 2011 09:18:42 +0000

Content-Type:

text/plain

Parts/Attachments:

Parts/Attachments

text/plain (82 lines)

Dear Allstat,

Senior Biostatistician
Permanent
Based in France (100% on site)
Excellent salary

A leading international pharmaceutical company has an outstanding opportunity for a permanent Senior Statistician to be based in their offices in Paris.

KEY RESPONSIBILITIES:

* Responsible for all statistical tasks on the assigned clinical trials, and perform these tasks with a high level of independence. For example, clinical trial design/planning, regulatory interactions, analysis plan, reporting activities, CTD and summary documents, exploratory analyses, and statistical consultation.
* May be assigned to lead a small project or parts (e.g., indication(s)) of a project, initially under the supervision/guidance of a more experienced statistician but with increasing autonomy and accountability.
* Track clinical trial/allocated project activities and milestones.
* Interact with the Method group as appropriate.
* Ensure timelines and adequate quality of all Biostatistics and Statistical Reporting deliverables for the assigned trials and project tasks.
* Follow processes and adhere to project specific standards as well as Health Authority requirements (SOPs, Master Analysis Plan, full development project specifications, and regulatory guidelines).
* Establish and maintain sound working relationships and effective communication within the Clinical Trial Team and B&SR team.
* Participate in or lead non-clinical project activities as needed.

Minimum requirements

* Master Degree in Statistics (or equivalent degree), or PhD in Statistics with pharmaceutical experience
* Experience in all tasks of a Trial Statistician
* Experience in Oncology Statistics and/or regulatory activities would be advantageous
* Fluent English (oral and written)
* Proven knowledge and expertise in statistics and its application to clinical trials
* Proven knowledge of drug development and Health Authority guidelines
* Knowledge of statistical software packages (e.g. SAS, S+)
* Good communication and presentation skills
* Good team player

For a confidential consultation call Laura Christie on +44 207 633 4825 or email your CV to [log in to unmask]

I look forward to hearing from you.

Kind regards,

Laura


Laura Christie
Principal Consultant, Biometrics, Europe
Recruiting experts in Pharma

HAYS Recruiting experts worldwide
25-27 Wootton Street
London
SE1 8TG

T:  +44 207 633 4825
M: +44 7900 932031
F: +44 207 922 7101
E: [log in to unmask]<mailto:[log in to unmask]>

hayspharma.com
------------------------------------------------




******************************************************************************
This message (including any attachments) is confidential and may be legally
privileged. If you are not the intended recipient, you should not disclose,
copy or use any part of it - please delete all copies immediately and notify
the Hays Pharma Helpdesk at [log in to unmask] .

Any information, statements or opinions contained in this message (including
any attachments) are given by the author. They are not given on behalf of
Hays Pharma unless subsequently confirmed by an individual other than the author who
is duly authorised to represent Hays Pharma.

Hays Pharma is a member of the Hays Plc group of companies. Hays Plc is registered in
England and Wales, number 2150950. Registered office, 250 Euston Road, London, England, NW1 2AF.
******************************************************************************

You may leave the list at any time by sending the command

SIGNOFF allstat

to [log in to unmask], leaving the subject line blank.

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