Hi AllSTAT,

Here at Syneos Health we have permanent opportunities for experienced Study Lead Statisticians 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.

For these positions we require people with a minimum education background of MSc or equivalent in a stats related subject. Extensive experience in statistical analysis of clinical or consumer health trials as demonstrated by the ability to lead multiple complex and/or global projects with teams of statisticians.


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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At Syneos Health we have exciting opportunities for Lead Statisticians experienced in clinical trials. We can consider people for Senior and Principal level positions to work with major global clients. This role can be home based and we will consider all EU locations.

 

 

Job Details:



• Act as the core project team lead to coordinate and manage all statistical project activities.

• Provide statistical liaison with the client.

• Provide statistical input for protocol and CRF development.

• Prepare statistical analysis plans.

• Perform validation and statistical quality checks on computer-generated output to verify accuracy.

• Review works performed by others and provide recommendations for improvement.

• Prepare and review key portions of the integrated clinical/statistical report, including sections related to data handling and statistical methodology, patient accountability, baseline comparability, and efficacy and safety results.

• Attend regulatory agency meetings and respond to questions to support the statistical analysis results of clinical trials on behalf of the sponsor.

• Undertake statistical consultancy for sponsor companies.

• Follow departmental SOPS, OGs and relevant regulatory guidelines (e.g. ICH).









Qualifications:



• Extensive experience in statistical analysis of clinical or consumer health trials as demonstrated by the ability to lead multiple complex and/or global projects with teams of statisticians

• Strong statistical skills as evidenced by participation in publications or presentations in areas relevant to clinical trial design and analysis

• Proficiency in SAS programming

• Excellent communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade

• Ability to travel may be required



In return we will offer: 

• A competitive remuneration package with excellent benefits.

• A commitment to your development and training, with the opportunity to progress your career within a market leading and innovative organization.

• The opportunity to work within a successful and rewarding environment





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