Seagen

Senior Clinical Data Programmer

Description

Summary

The Senior Clinical Data Programmer is capable of leading Data Management programming activities with minimal support and oversight. The Senior CDP is capable of creating, leading, and driving activities to assess and improve the Data Management programming infrastructure.

Requirements:

• Programs SAS Non-System Edit Checks and SAS Data Listings
• Ability to independently develop innovative and complex SAS programs to support activities including, but not limited to, data review and reporting
• Develops and maintains the Non-System Edit Check Global Library to ensure consistency across programs and studies and concordance with the EDC Global Library
• Trains Data Managers on how to create and review SAS program specifications, run SAS programs, review SAS logs, and generate output
• Works with Clinical Data Manager, Biomarker Data Specialist, Medical Monitor, and Protocol
• Lead (and other study team members as appropriate) to develop new or improve existing data review tools
• Coordinates with Data Managers regarding timelines and deliverables to ensure all SAS programs are working as expected
• Mentors less proficient Data Management SAS Programmers or other SAS users as appropriate
• Independently manage SAS processes and applications while evaluating for improvements; lead working groups to develop and implement new processes and applications
• May contribute to the development, review and implementation of SOPs, templates and processes and other departmental and/or cross functional initiatives
• Utilizes experience and leadership skills to provide guidance to other team members. Takes ownership of process resources available to team

Qualifications:

• Is fully conversant of SAS programming and best Clinical Data Management (DM) practices
• Knowledge of and experience with clinical databases, electronic data capture systems, quality control processes and auditing procedures
• Strong critical thinking skills
• Familiarity with GCP, ICH and FDA requirements as they apply to clinical data
• Strong well-rounded technical skills (EDC systems, MS Word, Excel, PowerPoint)
• Regular interaction with Data Management, Clinical Trial Management, and Medical Management groups
• Excellent written and oral communication skills
• Knowledge of industry standards (CDISC, SDTM, CDASH)
• 5-10 years of SAS programming experience in the pharmaceutical or biotechnology industry, depth and exposure to DM related tasks considered in lieu of a portion of the years of experience

Education

• Bachelors or higher in a health-related field
• SAS Certified Base Programmer for SAS 9 highly valued but not required

As the leading employer in our industry in the Pacific Northwest, Seagen is proud to offer a competitive total compensation package as well as a comprehensive benefits program designed to support the whole lives of our employees and their families. Benefits include medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, relocation assistance and much more. To learn more about Seagen, please visit www.seagen.com. 

Seagen is an equal opportunity employer. All qualified applications will receive consideration for employment without regard to race, age, gender identity, sexual orientation, color, religion, sex, marital status, national origin, protected veteran status, disability status, or any other status protected by federal, state, or local law. 

Apply:

Seagen

Seagen is an Equal Opportunity Employer

Submitted: 02/12/2021