Direct Client: SAS Clinical Programmer

SAS Clinical Programmer (References are a MUST) DIRECT CLIENT

North Wales, PA

1 Year Contract

Client is UTS >>> Siro Clinpharm

Rate: $45 to $50/hr DOE (Flexible for very Senior profiles)

Candidates recently worked with Merck please do not apply.

 

Our client is looking for a SAS Programmer who can undertake more complex programming assignments so as to ensure the efficient functioning of the programming unit and to develop SAS programs towards the validation of clinical data. Manage dedicated team (if required) and ensure quality and timeline compliance for deliverable and also to effectively manage the relationship with the client.

 

They are a leading full service Clinical Research Organization that specializes in providing solutions in clinical drug development. They have their Presence globally in countries like Germany, Greece, India, Israel, Malaysia, Romania, Spain and USA

 

In this position, the incumbent can expect to:

Creating and validating  SAS programs of datasets , tables, figures and listings (TFL) for safety and efficacy outputs in required format as per specifications provided by the client and/ or validating/debugging SAS reports in both Windows and Unix platforms 

Performing any other assigned activities towards programming in SAS for analyzing data in both Windows and Unix platforms 

Ensuring that timelines for deliverable across all projects are met for self and team members and they comply with established performance standards. 

Optimizing productivity and resource utilization across team members. 

Creation of programming specifications and provide support to other colleagues in this regard

 Conduct root cause analysis of reported issues 

Triage issues and address them to appropriate team in India. 

Resolve reported issues at level of Medical Monitoring SAS data set and I/J Review objects 

Ensuring a seamless flow of information and sharing of learning's across all teams. 

Providing guidelines for SAS Programming.

 

Specific Skills Required:

At least four years of relevant experience is essential in a CRO / Clinical Industry. 

About two years of experience in managing projects and teams. M.Sc. (Statistics), MCA, BE, M.Sc. (Life Sciences), M. Sc (Information Technology) 

Knowledge of statistical methods and application of those methods in Clinical Research.

BASE SAS Certification (desired)

 

References are a must

 

Thanks & Regards

 

David. P. Desai

Ida Solutions, Inc

david@idasolutions.net / david.sigma.p@gmail.com

http://www.linkedin.com/in/davidsigma

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