Sr. Statistical (SAS) Programmer
Company Name:
Talon
Our client, located in Fort Lee, NJ is seeking a Senior Statistical (SAS) Programmer for an immediate full-time position. Details include:
This is a position for a hands on Sr. Statistical (SAS) Developer. It has Manager level role.
-Summary of Responsibilities Provide statistical programming support to clinical trials for regulatory submissions and various publications posters etc.
-Support the Biostats function in statistical analysis including generating analysis data sets, patient listings, tables and figures for clinical trials.
-Develop and maintain the infrastructure for project files of SAS datasets and SAS codes
Essential Functions
-Develop SAS programs to produce analysis datasets.
-Write/Review data definition tables, data specs or related documents.
-Design /develop SAS macros and other utulities to expedite SAS programming activities.
-Knowledge and Skills: Indicate the education level, previous experience, specific knowledge, skills and abilities required to meet minimum requirements for this position.
Minimum education requirements
-Masters
Experience required
-5 - 7 Years
Knowledge & skills (general and technical)
-Proficiency in SAS/BASE, STAT, GRAPHICS and MACRO
-Extensive experience in creating data tables, figures and listings. documents and the analysis necessary to support electronic submissions and publications.
-Working familiarity with clinical trial design and analysis activities and knowledge of regulatory guidelines.
(FDA/CFR, ICH/GCP
Other requirements (licenses, certifications, specialized training, physical or mental abilities required) -Strong communication skills both oral and written. Strong organizational and time management skills and the ability to handle multiple assignments effectively and deal with ad hoc requests.
Confidential Data All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential.
Compliance Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of the client are carried out with the best industry practices and the highest ethical standards.
Mental/Physical Requirements Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time.
Ask our Talon Technology Occupational Consultants about our Referral Bonus Program.
Estimated Salary: $20 to $28 per hour based on qualifications.
Talon
Our client, located in Fort Lee, NJ is seeking a Senior Statistical (SAS) Programmer for an immediate full-time position. Details include:
This is a position for a hands on Sr. Statistical (SAS) Developer. It has Manager level role.
-Summary of Responsibilities Provide statistical programming support to clinical trials for regulatory submissions and various publications posters etc.
-Support the Biostats function in statistical analysis including generating analysis data sets, patient listings, tables and figures for clinical trials.
-Develop and maintain the infrastructure for project files of SAS datasets and SAS codes
Essential Functions
-Develop SAS programs to produce analysis datasets.
-Write/Review data definition tables, data specs or related documents.
-Design /develop SAS macros and other utulities to expedite SAS programming activities.
-Knowledge and Skills: Indicate the education level, previous experience, specific knowledge, skills and abilities required to meet minimum requirements for this position.
Minimum education requirements
-Masters
Experience required
-5 - 7 Years
Knowledge & skills (general and technical)
-Proficiency in SAS/BASE, STAT, GRAPHICS and MACRO
-Extensive experience in creating data tables, figures and listings. documents and the analysis necessary to support electronic submissions and publications.
-Working familiarity with clinical trial design and analysis activities and knowledge of regulatory guidelines.
(FDA/CFR, ICH/GCP
Other requirements (licenses, certifications, specialized training, physical or mental abilities required) -Strong communication skills both oral and written. Strong organizational and time management skills and the ability to handle multiple assignments effectively and deal with ad hoc requests.
Confidential Data All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential.
Compliance Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of the client are carried out with the best industry practices and the highest ethical standards.
Mental/Physical Requirements Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time.
Ask our Talon Technology Occupational Consultants about our Referral Bonus Program.
Estimated Salary: $20 to $28 per hour based on qualifications.
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