Hi AllSTAT,
Here at Syneos Health we have permanent opportunities for experienced Statistical Programmers throughout Europe. The roles can be home based from the start or if you prefer we can accommodate you in one of our many offices or how about a mix of the two!
We have positions available in client dedicated FSP teams and also in our full service business unit. You have the opportunity to experience all areas during your Syneos Health career.
We are looking for people with in-depth SAS experience in clinical trials. Who can be responsible for performing all SAS programming tasks required to support the conduct, statistical analysis and reporting of projects, and acts as the lead statistical programmer on multiple complex projects, providing leadership and technical expertise.
How To Apply:
If you have the above skills and would like to find out more, please reach to me at [log in to unmask] to find out more.
Many thanks
Jon
____________________________________________________________________
Jon Gibbs
Senior Talent Acquisition Specialist
Syneos Health
Tel: +44 1276 481027
Mobile: +44 7769 234292
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Why Syneos Health? Join a game-changing company that is reinventing the way
therapies are developed and commercialized. Created through the merger of two
industry leading companies, INC Research and inVentiv Health, we bring together
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You'll be supported with comprehensive resources based on today's emerging
technologies, data, science and knowledge - instead of practices from the past.
Teaming with some of the most talented professionals in the industry, you'll gain
exposure and work in a dynamic environment to over-deliver and outperform. A
career with Syneos Health means your everyday work improves patients lives
around the world.
Here at Syneos Health we are currently recruiting for a Senior or Principal Statistical
Programmer to join one of our client dedicated partnerships or Full Service teams in
EMEA. This role will mainly focus on statistical analysis and data handling.
Job Details:
* Act as the core project team lead to coordinate and manage all statistical
programming activities.
* Serve as the lead programmer to design and specify the overall approach to a
projects programming tasks.
* Provide statistical programming liaison to clients and input for Statistical
Analysis Plans.
* Create and maintain programming tracking documentation.
* Create, test, and maintain SAS programs for clinical studies.
* Generate summary tables, data listings, graphs and derived datasets as
specified in the statistical analysis plan.
* Generate outputs and reports to support other departments.
* Perform validation on computer-generated output to verify accuracy.
* Develop utility SAS macros for use in project programs.
* Performing validation on standard SAS macros.
* Transfer of deliverables.
* Following departmental SOPs, OGs, and relevant regulatory guidelines (e.g.
ICH).
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The ideal candidate will need the following experience / skills to be considered:
Undergraduate Degree, preferably in a scientific or statistical discipline
In lieu of degree, either community college diploma with initial programming
experience or SAS certified programmers
Extensive experience with SAS programming in a relevant clinical trial environment
as demonstrated by the ability to lead multiple complex and/or global projects with
teams of statistical programmers
Ability and skill in mentoring more junior staff
Proven ability to meet deadlines
Excellent communication, presentation, interpersonal skills, both written and
spoken, with an ability to inform, influence, convince, and persuade
We have a comprehensive benefits package and offer highly competitive
remuneration.
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