Sr. Statistical Programmer
- Boston, MA
Company Background
At MorphoSys, we are motivated by our mission: More life for people with cancer. As a global, commercial-stage biopharmaceutical company, we are driven by the urgency to discover, develop, and deliver groundbreaking medicines, aspiring to redefine how cancer is treated.
Our success is created by our people, and we bring together exceptional talent from around the world, offering our colleagues a collaborative, flexible, and diverse work environment. We are looking for individuals who share our values and are motivated to improve the lives of people impacted by cancer.
Since opening our U.S. office in Boston in 2019, we have doubled in size to support our rapid growth, building teams of experts across a variety of different disciplines, from drug development to commercialization.
To learn more, visit us at www.MorphoSys.com, and follow us on Twitter and LinkedIn.
Our success is created by our people, and we bring together exceptional talent from around the world, offering our colleagues a collaborative, flexible, and diverse work environment. We are looking for individuals who share our values and are motivated to improve the lives of people impacted by cancer.
Since opening our U.S. office in Boston in 2019, we have doubled in size to support our rapid growth, building teams of experts across a variety of different disciplines, from drug development to commercialization.
To learn more, visit us at www.MorphoSys.com, and follow us on Twitter and LinkedIn.
Job Summary & General Responsibilities
- Oversight and QC of CRO activities in:
- SDTM and ADAM Datasets development
- Table / Listing / Figure (TLF) development and validation based on the Statistical Analysis Plan
- TLF Mock shells development
- Working with data management in providing programming support for DM activities including data review
- Performing ad-hoc programming activities utilizing raw data based on internal and external requests
- Contributing in process development, reviewing and development of SOPs related to statistical programming activities
- Participate in Clinical Trial Teams, Data Review Teams, etc., and provide inputs from statistical programming perspective
- Communicating with and/or responding to internal cross-functional teams and clients for project specifications, status, issues or inquiries
- Collaboration with Statisticians and Data Management in planning study activities and ensuring study timelines are met
- Performing lead duties when called upon
Job Qualifications, Experience & Skills
- Ideally three or more years of experience in a Pharmaceutical company or a CRO as a SAS Programmer
- Bachelor´s or Master´s degree in Informatics, Mathematics, Medical Documentation or other relevant qualification
- Excellent ability in SAS data manipulation, analysis and reporting skills
- Extensive experience in implementing CDISC SDTM, CDISC ADaM, and Define standards
- Good knowledge of Table / Listing / Figure (TLF) programming, including SAS / STAT and SAS macro language and SAS graphic features
- Good understanding of descriptive and inferential statistics
- Proficient in industry standards, medical terminology and clinical trial methodologies
- Submissions experience utilizing define.xml and other submission documents is a plus
- Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
- Good communication skills and a good command of English language
- Ability to work under pressure, flexibility and adaptability
- Boston, MA
Full vaccination against COVID 19 is a requirement for this position.
EEOC Statement
MorphoSys US Inc. is an equal opportunity employer and complies with all applicable federal, state and local fair employment practices. We are committed to creating a diverse work environment with non-discrimination for all employees and qualified applicants without regard to race, color, religion, national origin, sex, protected veteran status or disability.