JOB | SAS Programmer
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* Experienced working within a clinical trials environment (Pharma, CRO), preferably Early Phase.
* Must be eligible to work in UK
Responsibilities and Duties
To lead the SAS Programming team and provide expert SAS Programming support to MAC Clinical Research and its customers.
To develop best working practices and Standard Operating Procedures to deliver the portfolio of projects within the SAS Programming Department.
Qualifications and Skills
* Educated to Degree level (or equivalent) in an area relevant to the role.
* Considerable demonstrable experience in SAS Programming and in-depth working knowledge of effective SAS Programming practices. Preferably, a minimum of 5 years in a SAS Programming role within the Pharmaceutical or CRO Industries.
* Demonstrable working knowledge of CDISC data standards including ADaM and SDTM.
* Excellent computer skills including expert use of SAS and other relevant programming software.
* Knowledge of drug development process including the relationship between the CRO industry and Pharmaceutical companies.
* Knowledge of clinical trial process; including the interaction between the SAS Programming team with the wider Biometrics team and clinical operations
Can be UK home-based with flexible working opportunities.
Opportunity to grow a team within a rapidly developing dynamic company.
Direct applications to [log in to unmask] or via website: www.clinicalresearchjobs.co
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