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ALLSTAT  February 2011

ALLSTAT February 2011

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Subject:

*** Hays Pharma - Permanent - Senior Statistician - Team Leader Statistics - Netherlands ***

From:

Laura Christie <[log in to unmask]>

Reply-To:

Laura Christie <[log in to unmask]>

Date:

Mon, 7 Feb 2011 10:59:31 +0000

Content-Type:

text/plain

Parts/Attachments:

Parts/Attachments

text/plain (88 lines)

Dear Allstat,

Please find below the latest permanent opportunity with Hays Pharma.

Senior Statistician - Team Leader Statistics
Permanent
Global Leading FMCG
Based in Netherlands (100% Client site)
Competitive salary

Job Description

-       Engages and collaborates with globally deployed, multi-disciplinary teams to design and implement efficient, well-focused, statistically fit-for-purpose clinical studies. Teams may include clinicians, measurement scientists, bioscientists, product formulators, claims experts, and other statisticians, both internal and external at CROs.
-       Though key responsibilities will be in area of clinicals studies, part of the work plan may comprise providing statistical expertise to the R&D program beyond clinical studies, for example, pre-clinical and product and consumer related studies and experiments.
-       Responsible and accountable for the overall statistical quality and defensibility of the statistical components and data interpretations from the study, whether or not they are implemented by others.
-       Directs and leads the technical statistical activities of other statisticians on clinical projects.  Reviews the input and implementation of others.
-       Insures that clinical studies are designed to address clear objectives, sufficiently powered with well-defined endpoints, and clear action standards.
-       Defines statistical approaches, identifies and/or develops appropriate statistical methodology, constructs and/or reviews/approves statistical analysis plans
-       Serves on protocol review committees for clinical studies as a statistical expert, and provides statistical input on claims substantiation
-       Interfaces and oversees relationships with external statisticians on outsourced statistical components, managing technical and non-technical aspects of statistical collaborations.
-       Manages the day-to-day deployment of statistical resource, both internal and external, for the benefit areas that he/she is in charge of, and recommends which studies will be outsourced.
-       Liaises with Global Data Sciences Leadership Team members and other statisticians on statistical quality issues in clinicals
-       Provides effective, knowledgeable links to regulatory aspects of clinical endeavor as it pertains to good clinical practice, e.g. ICH, FDA requirements and processes, and brings these aspects into play on relevant clinical studies
-       Conducts investigations across studies to better understand variation of substrate measurement system, and target population on efficacy variables, in order to improve the design of future studies
-       Identifies new/novel statistical methodology and reduces it to practice where it can add quality and value to the clinical endeavour
-       Mentors other statisticians and scientists

Minimum Requirements

-       Master's Degree or PhD (preferred) in Statistics or Biostatistics
-       Must have extensive industry experience i.e. in clinical research, with some Pharma experience and regulatory process understanding
-       Exceptional technical depth, operational breadth and demonstrated fluency in biostatistics approaches applied to clinical research
-       Hands-on with diverse statistical software including SAS and JMP
-       Strong interpersonal, communication, oral and written, excellent negotiating and influencing skills previously demonstrated in a complex, challenging organisational environment
-       Demonstrated ability to resolve ambiguity and propose, gain buy-in, and deliver effective solutions against aggressive timelines; highly driven to deliver on in
-       Demonstrated ability to adapt to the communication style of others in order to maximize impact
-       Ability to collaborate effectively in global teams across time-zones and cultures

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

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