Closing Date: 17 Mar 17
Salary (£): Competitive
Benefits: Comprehensive package
Due to our continuing success and expansion, we are currently looking for an experienced Biostatistician to work with our team - flexible locations in Germany
Chiltern is the leading, global mid-sized contract research organization. We listen to client needs to deliver customized clinical development solutions with a team of more than 4,000 working across 47 countries to provide comprehensive, yet flexible and responsive, services. Our specialties include Clinical Development, Oncology, Device & Diagnostics, Data, Analytics & Evaluation and Strategic Service Provision.
Due to our continuing success and expansion, we are currently looking for an experienced Biostatistician to work with our Clinical Analytics group. Office based or homebased in GERMANY.
Clinical Analytics is a unique and well established business unit within Chilterns’ Strategic Staffing Provision that provides Biostatistics, Data Management and Statistical Programming solutions to some of the largest Pharmaceutical companies globally.
As part of these diverse partnering models we can offer all the benefits of working for a dedicated CRO whilst gaining exposure to the Pharmaceutical sector. Chiltern is also a dedicated partner and leader in CDISC standards and compliance. We offer a great place to learn and develop strong CDISC skills and the goal of our team is to develop global CDISC leaders.
This role would be suitable for either an experienced Senior Biostatistician or Principal Biostatistician, depending on experience level.
SUMMARY OF POSITION:
Plan, analyse and summarize the results of individual clinical studies or groups of studies (integrated summaries) and coordinate the development and review of regulatory submissions (e.g., NDAs). Program and/or review statistical tables, listings, figures, and analysis datasets for clinical trials in accordance with Chiltern and/or sponsor Standard Operating Procedures (SOPs) or study specific guidelines. Manage and/or mentor junior level biostatistics staff.
Master’s degree, equivalent, or higher in Biostatistics or related field
Extensive experience in statistical design and analysis methodology or basic and complex studies
Extensive experience in leading statistical activities in clinical research
Experience with regulatory submissions and support preferred
Ability to program in one or more statistical software packages (SAS® preferred) used to conduct statistical analyses
Excellent verbal and written communication
Proven ability to effectively communicate statistical concepts
Previous experience in a pharmaceutical research or CRO setting required
Some supervisory experience preferred
Exhibited a positive attitude and willingness to learn and lead in a team setting
A satisfactory combination of education and experience may be accepted as a substitute for the specific education and experience listed.
To apply, please send your CV to firstname.lastname@example.org
For more extensive information about Chiltern, please visit our web site at www.chiltern.com
Please note: Agency applications will not considered. Candidates who do ot have the required experience may nt recieve a response.
171 Bath Road Slough Berkshire
SL1 4AA, UK
|Tel:||+44 (0) 1753 512000|
|Fax:||+44 (0) 1753 511116|
|Website:||Visit Our Web Site|
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.