Détails du poste

It’s More Than a Career, It’s a Mission.

Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.

Our Mission

People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.

What We Need:

COMPANY: Sarah Cannon Research Institute Holdings, LLC (Joint Venture with McKesson Corporation)

POSITION: Statistical Programmer II

LOCATION: 6555 State Highway 161, Irving, TX 75039

JOB DUTIES: Create, review and approve annotated CRF to SDTM datasets. Responsible for the translation of the SAP into programming specifications for analysis data model (ADaM) datasets. Review and provide input on key study-related documents produced by other functions, such as case report forms, data management plan, statistical analysis plan and TFL specifications. Responsible for the development, review, validation, and execution of SAS programs to generate standard (SDTM and ADaM) and non-standard (custom study specific) datasets as defined in specifications documents. Responsible for the development, review, validation, and execution of SAS programs to generate presentation-ready outputs (i.e., Tables, Figures, and Listings), as defined in the statistical analysis plan. Write and validate study and product-level macros and utilities. Ensure accuracy, quality, and timeliness of all work completed for the project. Program the integration of databases from multiple studies or sources. Responsible for accuracy and reliability of results. Builds and monitors quality in every aspect of job activities. Communicate effectively within a multi-disciplinary project team and external resources to complete assigned tasks on time and within budget. Ensure an awareness and familiarity with the types of risks associated with a study and the impact on the quality of deliverables. Function as Lead Programmer on one or more clinical trials. Provide project deliverable oversight, guidance and direction to the programming team. Provide guidance in programming for complex analysis tables and figures, appropriate procedure and method selection for advance statistical analyses. Ensure all programming activities on the study adhere to required standards. Provide input to and participate in team meetings. 100% telecommuting allowed from anywhere in the United States.

REQUIREMENTS: Master’s Degree, or foreign equivalent, in Industrial and Human Factors Engineering, Statistics, Computer Science, Engineering or a related field and one (1) year of experience in the job offered or related occupation.

Experience must include one (1) year in the following skills:

• Base SAS Functions and Procedures;
• SAS / SQL;
• SAS / Macro;
• SAS / STAT;
• CDISC SDTM / ADAM Standards Define.xml; and
• Working with SAS Software.

OFFERED WAGE: $85,600 -$142,800/year

CONTACT:  To apply, please send resumes to JobPostings@McKesson.com. Reference #: 002062

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.