Remote

Position Summary:

The Principal SAS Programmer programs metrics, reports and tools for the support of the clinical trial data cleaning process from study start up to post database lock for assigned projects using the SAS software.

Essential functions of the job include but are not limited to:

Maintains the full-scope of responsibility for assigned projects: ensures on-time delivery, communicates the status of projects to internal teams and study
Provides collaborative input and guidance to the design of SAS outputs to the client and internal teams
Programs metrics, reports, tools, patient profiles
Develops, tests, and validates SAS programs to support client-related and cross[1]functional projects.
Troubleshoots and resolves SAS program issues
Develops and maintains SAS programming validation documents
May provide biostatistics support for client-related projects which may include tables, listings, figures, SDTM, ADaM and various other CDISC deliverables
May provide data management support for client-related projects from CRF design to post database close and archival
Participate in conducting demonstrations and trainings
Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to SAS programming activities
Provide leadership for cross-functional and organization-wide initiatives, where applicable
Train project team members
Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues
Present software demonstrations/trainings, department/company training sessions, present at project meetings
Requires some travel
May perform other duties as assigned

Qualifications:

Minimum Required:

12+ years’ experience
Bachelor's degree or equivalent in local country or equivalent level of experience
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook.
Able to handle a variety of clinical research tasks.
Excellent organizational and communication skills
Professional use of the English language; both written and oral.
Experience in utilizing various clinical database management systems
Experience in a clinical, scientific or healthcare discipline
Advanced computer skills • Base SAS®, SAS/STAT and SAS/ACCESS
SAS Macro Language • Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.…)
Broad knowledge of drug, device and/or biologic development and effective data management practices
Strong leadership and interpersonal skills

Preferred:

Experience in Object Oriented Programming (C#, C++, VBS, etc.), scripting language (PERL, etc.), R, SQL
Oncology and/or Orphan Drug therapeutic experience

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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

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