Dear Allstat,
Please find below our latest contract vacancy:-
FREELANCE: Statistical Programmer
6 month rolling contract
Mainland Europe (100% Client site)
Excellent hourly rate
Job Description:
* Manage the programming activities for a global project following internal guidelines
* Act as lead Statistical Programmer for assigned projects and take a programming leadership role on the project team
* Maintain efficient interfaces with internal and external customers with advice from management and the Statisticians
* Develop and comply with project / study standards and specifications following internal and regulatory guidelines
* Oversee programming style, quality of contributions and compliance with timelines.
* Provide input and lead sections of submissions in coordination with Statistician.
* Ensure that documents and specifications are consistent and comply with company standards by providing input into study protocol, CRF and data structures.
* Program, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials
* Ensure quality control and quality audit of deliverables
* Maintain records for all assigned projects and archive trial / project analysis and associated documentation
* Participate in the selection of CROs, as required, and supervise project activities for CROs
* Train staff on trial and project level activities and internal processes
* Participate in or lead process improvement initiatives and non-clinical project activities
Minimum Requirements:
* BSc or MSc in Mathematics, Statistics or Biostatistics
* Must have extensive industry related experience
* Expert knowledge of / experience with SAS software.
* Good understanding of global clinical trial practices, procedures, methodologies
* Good understanding of regulatory requirements (e.g., GCP, ICH).
* Ability to supervise others
* Experience in providing recommendations for maintenance or development of global policies, procedures and clinical data presentation standards
* Intermediate knowledge of office tools
* Must have working experience with implementation, usage and possibly training in SDD (SAS DRUG DEVELOPMENT)
For a confidential consultation call Laura Christie on +44 203 465 0083 or email your CV to [log in to unmask]<mailto:[log in to unmask]>
A more detailed job spec available on request.
I look forward to hearing from you.
Kind regards,
Laura
Laura Christie
Team Leader, Biometrics & HEOR, Europe
Recruiting experts in Life Sciences
HAYS Recruiting experts worldwide
107 Cheapside
London
EC2V 6DB
T: +44 203 4650 068
M: +44 7900 932031
F: +44 203 465 0001
E: [log in to unmask]<mailto:[log in to unmask]>
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