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JOB STATEMENT
The primary focus of this position is to perform and lead statistical programming tasks associated with Phase 1, 2, 3 and 4 clinical trials for new drug and biological products, as well as medical devices.ESSENTIAL JOB FUNCTIONS
• Develop policies and procedures.
• Provide leadership and work on multiple clinical projects
• Train/mentor statistical programmers.
• Successful completion of programming tasks on time and on budget
• Expected to provide leadership in new technologies and procedures for improved efficiencies.
• Design, develop and test SAS software to implement Program Analysis Specifications (PAS) for multiple projects.
• Document and validate SAS software development according to Biostatistics standard operating procedures.JOB REQUIREMENTS / EDUCATION / EXPERIENCE
• Bachelor or Master’s degree in a scientific discipline, preferably Statistics or Computer/Health Science.
• Minimum of three to five years Statistical Programmer Analyst III experience relevant biopharmaceutical industry experience.
• Ability to train/mentor statistical programming support staff.
• Knowledgeable about regulatory and ICH Guidelines as it pertains to project support.
• Excellence in interpersonal, verbal and written communication skills a pre-requisite for advancement.
LOCALE:
Atlanta, GA
COMPENSATION:
to 85k plus full benifitsHOW TO APPLY
Send your resume to steve.pruner[at]clinimetrics.com
Discussion forums: Opportunity: Sr. Analytical SAS Programmer/Analayst - Full-time Perm position in Atlanta office, Atlanta GA (US)
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