Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutchs pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nations first cancer prevention research program, as well as the clinical coordinating center of the Womens Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.
At Fred Hutch, we believe that the innovation, collaboration, and rigor that result from diversity and inclusion are critical to our mission of eliminating cancer and related diseases. We seek employees who bring different and innovative ways of seeing the world and solving problems. Fred Hutch is in pursuit of becoming an antiracist organization. We are committed to ensuring that all candidates hired share our commitment to diversity, antiracism, and inclusion.
The Statistical Center for HIV/AIDS Research and Prevention (SCHARP) at Fred Hutch is a full service statistical and data management center focused on HIV prevention research. SCHARP has an annual budget of over $40 million, more than 180 employees and is currently managing over 40 active phase I III clinical trials in over 150 clinical sites around the world. SCHARP is seeking an EDC Report Programmer role to support both the EDC Programming and Clinical Data Management teams through the development of data reporting requirements and the programming of study reports using Business Objects or other software package(s). This position will also translate data management specifications for data entry screens, edit checks, custom functions, data integrations, and test plans for clinical study builds in the Clinical Data Management system. Responsibilities - Configure reports using of Medidata Rave Business Objects and other software
- Create standard, study-specific, and ad hoc reports with high attention to detail, accuracy, and timeliness
- Test and debug reports as well as maintain version control on production reports and scripts
- Document requirements related to all data and reporting needs such as dashboards, scorecards, reports, ad hoc queries, and other data needs
- Create user acceptance testing (UAT) criteria for reports. Validate reports against UAT criteria
- Configure and program clinical trial forms, visit schedules, edit checks and other study requirements in EDC systems using applied knowledge or programming and data standards
- Performs verification of quality and completeness of study deliverables prior to release
- Performs peer review for configuration and programming completed by other EDC programmers for both new study builds and post-production changes
- Support EDC programming requests from study teams as assigned, applying knowledge of EDC tools and data standards to complete requests in the timelines defined
- Supports other activities as assigned
Qualifications Minimum qualifications - Bachelors degree in computer science, or a scientific, technical, or health-related field
- At least 3 years of experience is required in report programming
- Demonstrated programming skills (SQL, or similar programming experience)
- Fundamental understanding of clinical trials
- Working knowledge of relational database management system
- Excellent written & oral communication skills including grammatical/ technical writing skills
- Effective time management and organizational skills
- Must work well independently and be self-motivated
- Candidates should be detail-oriented with strong analytical and critical thinking skills
- Experience in good clinical data management practices in health research
- Experience with EDC software
- Experience with Data Management tools or best practices
Preferred qualifications - Experience working in a biomedical laboratory and/or experience with clinical trials and data management
A statement describing your commitment and contributions toward greater diversity, equity, inclusion, and anti-racism in your career or that will be made through work at Fred Hutch is requested of all finalists. Our Commitment to Diversity We are proud to be an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. We are committed to cultivating a workplace in which diverse perspectives and experiences are welcomed and respected. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability (physical or mental), marital or veteran status, genetic information, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We are an Affirmative Action employer. We encourage individuals with diverse backgrounds to apply and desire priority referrals of protected veterans. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to our Employee Services Center at hrops@fredhutch.org or by calling 206-667-4700. |
