This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message for pharmaceutical industry jobs
Fforde Management is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Senior Clinical Data Manager
Principal Biostatistician (Home Based)
United Kingdom
CRA (m/w) in Deutschland, Schwerpunkt Onkologie
Senior Biostatisticians - Reading or Home based
South East
Ireland (Eire)

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister site:
Our sister site
Job Details
This job has expired. Click here to view similar jobs.

Contract Project Statistician - Europe

Business Type: Clinical Research Organisation
Job Type: Data Management, Statistic - Biostatistics, Clinical Study- Trials
Job Level: Not Specified
Position: Contract
Salary: Competitive
Location: United Kingdom
Reference: 17528/003
Closing Date: 24/07/12
Our client is committed to developing a growing portfolio of superior pharmaceutical-based health care solutions with breakthrough medicines for conditions such as depression, schizophrenia, attention-deficit hyperactivity disorder, diabetes, osteoporosis and many more. They are currently seeking Project Statistician for a 12 month contract that can be based in UK, Germany, France or Spain.

The Project Statistician will develop or provide oversight in the development of study protocols and data analysis plans in collaboration with physicians, and/or medical colleagues. They will be responsible for working with research associates and scientists to oversee the establishment of a reporting database and the analyses of study data. Furthermore, the Project Statistician will lead the study team on their interpretation of results and will be co-author for internal or external publication of the results.

Writing statistical parts of protocols for clinical trials and/or observational studies;
Assisting in or is accountable for selecting statistical methods for data analysis;
Coordinating the statistical programming with CRO statisticians and communicates accordingly with the CRO;
Collaborating with data management in the planning and implementation of data quality assurance plans;
Supporting medical affairs in the statistical aspects of designing, implementation and results interpretation of patient support programs;
Collaborates with team members to write reports and communicate results;.
Assisting with or is responsible for communicating study results via regulatory submissions;
manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings;

M.S., Ph.D., or equivalent experience
Statistics, Biostatistics, or equivalent of field study

Leadership and teamwork skills
Strong interpersonal communication skills
Knowledge of the SAS programming language

Fforde is acting as a recruitment agency/business.

Project Management, Statistician, Statistics, Study, Clinical Research, Biostatistics, Data Management, Clinical Trials, Clinical Studies, Data Analysis, Programming, Quality Assurance, QA, Medical Affairs, MS, PhD, Degree, Pharmaceutical, CRO, UK, Paris, France, Hamburg, Germany, Paris, France, Europe

Posted: 26/06/2012 | NPJ Ref: 83464
line graphic

Compatible with:

JobMate   Broadbean

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing

Credit cards image