(5+ yrs) Oncology Senior Clinical Data Specialist - Full Time

MRO Corporation; Oregon; Ibrido; USD 47.000 - 51.000; Tempo pieno

Descrizione del lavoro

MRO Corporation seeks a Senior Clinical Data Specialist to deliver high-quality oncology data solutions to hospital partners nationwide, drawing on deep cancer registry experience and a commitment to quality and learning.

Team members must commit to at least 30 hours per week, with educational opportunities and CEUs supported by our Quality & Education team.

Competenze

• Active Oncology Data Specialist (ODS) Certification.
• 5+ years experience abstracting with an ODS certification.
• Intermediate proficiency with MS Office (Microsoft Excel and outlook).

Mansioni

• Abstract, code, and report oncology data from unstructured medical records per registry standards.
• Ensure high-accuracy data submissions.
• Support CoC Accreditation through cancer registry operations and quality tools.

Conoscenze

Cancer program accreditation

EMR systems

Data analysis

Attention to detail

Learning new systems

Time management

HIPAA compliance

US work eligibility

Formazione

ODS Certification

5+ years ODS experience

MS Office proficiency

Strumenti

EMR systems

Clinical databases

Descrizione del lavoro

Overview Join us in advancing safer, consistent, quality healthcare for all.Job Summary:The Senior Clinical Data Specialist plays a key role in delivering high-quality oncology data solutions to hospital partners nationwide. This is a unique opportunity to become a part of our team during a milestone moment in our growth, benefiting from our deep cancer registry experience and employee-centric leadership. Team members must be willing to commit to working a minimum of 30 hours per week.

Responsibilities

• Abstract, code, and report oncology data from unstructured medical records in alignment with state and national cancer registry standards.
• Ensure quality submission of all data , maintaining a high accuracy threshold.
• Support hospital partners' CoC Accreditation process through strong cancer registry operations, policy development, and utilization of NCBD quality tools and standards.
• Engage in educational opportunities and on-the-job learning through CEUs and dedicated learning time, supported by our internal Quality & Education team.
• Stay current on regulatory/publicly reported data requirements as specified by federal, state, payer, and other agencies.
• Collaborate on team best practices, data dictionaries, abstraction guidelines, and process improvement initiatives.
• Contribute to a culture of perpetual learning and meaningful collaboration, supporting newer team members, including recently certified ODS-Cs and Clinical Data Support Specialists.

Qualifications

Required Skills/Abilities

• Strong understanding of cancer program accreditation and other applicable standards.
• Experience working with multiple patient medical record systems (EMRs) and clinical databases.
• Strong analytical and critical thinking skills to approach medical data analysis.
• High attention to detail.
• Technically savvy and open to learning new systems and technology.
• Organized and adept at time management; comfortable balancing multiple projects.
• Committed to data and information security and HIPAA compliance ( Q-Centrix is SOC2 + HITRUST certified).
• Must be legally able to work in the United States now or in the future without sponsorship.

Education and Experience

• Active Oncology Data Specialist (ODS) Certification.
• 5+ years experience abstracting with an ODS certification.
• Intermediate proficiency with MS Office (Microsoft Excel and outlook).

Pay Range

USD $34.00 - USD $37.00 /Hr.