Statistical Programmer II
INC Research is a top-tier therapeutically focused global clinical research organization (CRO) providing a complete range of Phase I - Phase IV clinical development services for the world’s biopharmaceutical companies. We proudly boast 43 of the world’s top 50 pharmaceutical companies as our customers. With approximately 5,000 employees across six continents and experience spanning more than 100 countries, we provide significant scale, scope and expertise to deliver innovative clinical development approaches and strategic alliances that meet the needs of our customers.
As Statistical Programmer II, you will be responsible for
Working under the supervision of a Lead Statistical programmer, participates in the programming and quality control of mapped and analysis datasets, tables, listings, and figures and other programming activities as assigned. May serve as Lead Statistical Programmer for projects of low to moderate complexity. Participates in the creation and maintenance of Statistical Programming project documentation.
Core Responsibilities
1. Uses SAS software (BASE, STAT, GRAPH, MACRO) for the production of well formatted datasets, tables, listings, and figures, and outputs requested (e.g., patient profiles) per programming specifications, Statistical Analysis Plan, and other study related documentation.
2. Performs Quality Control to ensure that outputs meet quality standards and project requirements. Works with Programmer, Biostatistician, and other project team members to resolve discrepancies or any findings.
3. Develops specifications for outputs of low to moderate complexity and well-presented mock-up displays for tables, listings, and figures of any complexty according to statistical and Sponsor requirement. Anticipates and addresses potential programming issues, reflects forethought, establishes the basis for efficient programming, accurately defines all variables to be accepted by peer review and sponsor/requestor with little rework
4. May act as the Lead Statistical Programmer, directs the programming activities of other programming personnel and monitors progress on programming deliverables.
5. Negotiates and establishes accurate time estimates for completion of study programming activities with internal team members and Statistical Programming management and completes project programming activities within timeframe allotted.
6. Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload. Keeps project team members informed of programming progress and issues requiring their attention.
7. Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs in compliance with Company and sponsor standards.
8. Regularly attends and prepares in advance for internal and external team meetings, contributes ideas and demonstrates respect for opinions of others.
9. Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.
Skills & Attributes
We are seeking candidates with the following key attributes:
BS, MS, or equivalent in Mathematics, Statistics, Computer Science, or related field. Minimal experience in SAS programming or equivalent combination of education and experience. Experience with clinical trials preferred. Effective written and verbal communication skills. Ability to read, write, speak, and understand English.
Company Profile: INC Research:
We provide competitve salaries, comprehensive benefits packages and the support and training available from working with a top ranking and award winning CRO.
As one of the fastest-growing global providers of Phase I-IV services we offer experience spanning the globe, along with retention capabilities and broad therapeutic expertise, to meet our customers' clinical development challenges.
Apply for this Job
INC Research is a top-tier therapeutically focused global clinical research organization (CRO) providing a complete range of Phase I - Phase IV clinical development services for the world’s biopharmaceutical companies. We proudly boast 43 of the world’s top 50 pharmaceutical companies as our customers. With approximately 5,000 employees across six continents and experience spanning more than 100 countries, we provide significant scale, scope and expertise to deliver innovative clinical development approaches and strategic alliances that meet the needs of our customers.
As Statistical Programmer II, you will be responsible for
Working under the supervision of a Lead Statistical programmer, participates in the programming and quality control of mapped and analysis datasets, tables, listings, and figures and other programming activities as assigned. May serve as Lead Statistical Programmer for projects of low to moderate complexity. Participates in the creation and maintenance of Statistical Programming project documentation.
Core Responsibilities
1. Uses SAS software (BASE, STAT, GRAPH, MACRO) for the production of well formatted datasets, tables, listings, and figures, and outputs requested (e.g., patient profiles) per programming specifications, Statistical Analysis Plan, and other study related documentation.
2. Performs Quality Control to ensure that outputs meet quality standards and project requirements. Works with Programmer, Biostatistician, and other project team members to resolve discrepancies or any findings.
3. Develops specifications for outputs of low to moderate complexity and well-presented mock-up displays for tables, listings, and figures of any complexty according to statistical and Sponsor requirement. Anticipates and addresses potential programming issues, reflects forethought, establishes the basis for efficient programming, accurately defines all variables to be accepted by peer review and sponsor/requestor with little rework
4. May act as the Lead Statistical Programmer, directs the programming activities of other programming personnel and monitors progress on programming deliverables.
5. Negotiates and establishes accurate time estimates for completion of study programming activities with internal team members and Statistical Programming management and completes project programming activities within timeframe allotted.
6. Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload. Keeps project team members informed of programming progress and issues requiring their attention.
7. Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs in compliance with Company and sponsor standards.
8. Regularly attends and prepares in advance for internal and external team meetings, contributes ideas and demonstrates respect for opinions of others.
9. Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.
Skills & Attributes
We are seeking candidates with the following key attributes:
BS, MS, or equivalent in Mathematics, Statistics, Computer Science, or related field. Minimal experience in SAS programming or equivalent combination of education and experience. Experience with clinical trials preferred. Effective written and verbal communication skills. Ability to read, write, speak, and understand English.
Company Profile: INC Research:
We provide competitve salaries, comprehensive benefits packages and the support and training available from working with a top ranking and award winning CRO.
As one of the fastest-growing global providers of Phase I-IV services we offer experience spanning the globe, along with retention capabilities and broad therapeutic expertise, to meet our customers' clinical development challenges.
Apply for this Job
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