WHO WE ARE

Keyrus Life Science is an international Consulting, Contract Research Organisation and Functional Services provider with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our human approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.
At Keyrus Life Science we’re proud of our commitment to deliver services of the highest quality, not only skillfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services

ROLE

The clinical statistical programmer will be responsible for providing study level statistical expertise hand to hand with the other statistical team member
The clinical statistical programmer will also be responsible for Providing statistical programming expertise to the development, validation and supporting Clinical development and Medical team.

KEY RESPONSIBILITIES:

• Programming deliveries through preparation of clinical datasets for regulatory submissions.
• Writing and executing SAS programs for data analysis and reporting.
• Performing statistical analysis such as normalization, linear regression, non-linear regression and hypothesis testing for different biological assay data with various plates formats in drug discovery process.
• Responsible for statistical programming activities. That includes, but is not limited to: analyzing, integrating and reporting of clinical trial data in order to produce quality and timely deliverables.
• Responsible for statistical programming activities in order to produce adequate and timely deliverables.
• Provide statistical programming support for clinical studies through generation of derived analysis data sets, tables, listings, and figures, including quality control of those documents.
• Participating in operations meetings and address issues that may influence statistical programming and data management.
• Coordinating programming activities for the client
• Development/validation of study specific and cross project macros
• Performing/validating statistical analysis and compiling those into statistical reports including interactive graphical outputs.
• Input in standard processes (review of Standard Operating Procedures, guidelines, definition of new processes needed)
  Initial length of contract: 20 hours/week ( but might be growing with time) 1 year and renew each year
  Start date : as soon as possible.