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Sr SAS Programmer

extra holidays - extra parental leave

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

United Kingdom

Offer summary

Qualifications:

Bachelor's degree or equivalent experience, 3+ years in clinical or healthcare discipline, Broad knowledge of drug/device development, Proficient in Base SAS® and SAS Macro Language, Familiarity with Microsoft Office.

Key responsabilities:

Develop and maintain SAS programming for clinical data support
Provide input on metric and reporting design
Develop proprietary patient profiles and data visualizations
Ensure on-time project delivery and status communication
Test, validate SAS programs, and lead training sessions.

Precision For Medicine Biotech: Biology + Technology Large https://www.precisionformedicine.com

1001 - 5000 Employees

See more Precision For Medicine offers

Job description

Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe.

Position Summary:

Are you interested in a unique and challenging role applying your SAS programming skills? We are looking to combine your SAS programming skills and ideas with our Data Manager expertise to produce the critical tools and outputs that make a clinical trial successful! We understand the power of SAS in the day-to-day management of clinical trial data are and looking for programmers interested in non-SDTM and ADaM dataset and TLF programming to join our amazing team.

Focused on developing and maintaining SAS programming to support the review of clinical data as part of a cross-functional data review and cleaning approach
This is not standard statistical programming including generation of SDTM and ADaM datasets and TLFs to support the formal analysis of clinical trial data

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

Provides collaborative input and guidance to the design of SAS outputs to the client and internal teams to develop metrics, reconciliation reports, tools, listings and standard patient profiles

May support the development of complex proprietary patient profiles designed to facilitate efficient holistic data review & centralized monitoring, aggregate data review workbooks, metrics, projections, graphs and other data visualizations including the application of oncology disease assessment criteria, CTCAE criteria, etc.
Ensures on-time delivery, communicates the status of projects to internal teams and study

Develops, tests, and validates SAS programs to support client-related and cross-functional projects
Troubleshoots and resolves SAS program issues
Develops and maintains SAS programming validation documents
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
May provide leadership for cross-functional and organization-wide initiatives, where applicable
May 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
May require some travel
May perform other duties as assigned

Qualifications:

Minimum Required:

Bachelor's degree or equivalent in local country or equivalent level of experience

Minimum of 3+ years of experience in clinical, scientific or healthcare discipline

Other Required:

Broad knowledge of drug, device and/or biologic development and effective data management practices
Base SAS®, SAS/STAT and SAS/ACCESS software
SAS Macro Language
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
Excellent organizational and communication skills
Professional use of the English language; both written and oral
Experience in utilizing various clinical database management systems (EDC)

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

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