Dear Allstat,
Cytel is shaping the future of drug development!
We are widely regarded for our pioneering work in adaptive clinical trials and as the world's largest biometrics CRO, we collaborate with leading pharmaceutical, biotech and medical device companies helping them to improve clinical success rates via optimal study design, effective data management, accurate statistical analysis and software.
Due to recent exponential growth on a global scale we are currently hiring:
* Principal Statistical Programmers
* Permanent or Contract
* Locations: UK, Switzerland, France, Spain, Germany or Poland
Reporting to the Director, Statistical Programming, you will have an opportunity to step into an exciting role supporting or leading one or more Phase I-IV clinical trials across a variety of therapeutic areas.
How You Will Contribute
* Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming;
* Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs);
* Production and QC / validation programming;
* Generating complex ad-hoc reports utilizing raw data;
* Applying strong understanding/experience of Efficacy analysis;
* Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries;
* Performing lead duties when called upon;
* Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.;
* Being adaptable and flexible when priorities change
What You Offer
* Bachelor's degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc.
* Highly experienced in SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry.
* Study lead experience
* Strong SAS data manipulation, analysis and reporting skills.
* Solid experience implementing the latest CDISC SDTM / ADaM standards.
* Strong QC / validation skills.
* Good ad-hoc reporting skills.
* Proficiency in Efficacy analysis.
* Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
* Submissions experience utilizing define.xml and other submission documents.
* Experience supporting Oncology studies would be a bonus.
* Excellent analytical & troubleshooting skills.
* Ability to provide quality output and deliverables, in adherence with challenging timelines.
* Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
What We offer
* A collaborative, data driven, international working environment that encourages innovation and rewards results
* Exposure to new and challenging projects within our thriving Functional Service Provider (FSP) or Project Based Service (PBS) divisions
* Partnership with respected experts and leaders in the fields of biostatistics and statistical programming contributing to the delivery of life changing medicines
For more information on this opportunity or if you would like to find out about our organisation and current openings, please contact me directly on +44 (0) 1444 242 220 or reach out to me via [log in to unmask]<mailto:[log in to unmask]>.
I look forward to hearing from you.
Anetta Kotynska
Recruiter
T: +44 (0) 1444 242 220
This email and any attachments are confidential and may be legally privileged. If you received this e-mail in error, please notify the sender immediately by return e-mail and delete this message and any attachments. You may contact Cytel Inc by visiting www.cytel.com/about-us/.
You may leave the list at any time by sending the command
SIGNOFF allstat
to [log in to unmask], leaving the subject line blank.
|