Hello Allstat
I hope this email finds you well. I've seen these posts advertised by some other companies too so if you have already applied apologies for reposting this. However if you would like to apply please find details of this role below:
As the successful candidate, you will:
- Coordinate programming activities across several trials with a given compound including publication and regulatory submission activities.
- Develop programming specifications for analysis datasets, pooled datasets and deliverables in consultation with the statistician.
- Develop and comply with project/study programming standards and specifications following internal guidelines
- Program according to specifications, analysis datasets, pooled datasets, listings, and figures for clinical trials and submission activities
- Support quality control and quality audit of deliverables
- Provide input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities
- Track clinical trial milestones for statistical reporting deliverables.
- Maintain records for all assigned projects and archiving of trial/project analysis and associated documentation.
- Maintain efficient interfaces with internal and external customers and communicate effectively across line functions.
The rates on offer are extremely good and the deadline for applications is Wednesday March 29th
I am also recruiting for 3 SAS Programmers in the same company for 6 months on a very good rate also, so if you feel that this role interests you but is a little too senior at the moment it is also worth applying for the other roles.
Thank you and I hope to speak with you soon.
All the best
Jonathan
Jonathan Hart-Smith
Managing Director
CK Clinical Limited
9 High Street
Stevenage
SG1 3BG
DD: 0845 034 3082
T: 01438 743047
M: 07985 152216
Internal: 2019
F: 01438 723800
W: www.ckclinical.co.uk
Follow me on TWITTER. Username: CKClinical
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