Technical Specialist I
Role details
Job location
Tech stack
Job description
The Technical Specialist I is responsible for:
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Researching, developing, interpreting and delivering Surveys, Anatomic Pathology Education and Quality Management programs (Surveys) and scientific committee projects to meet customers' needs and support CAP objectives.
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Assisting with communication and consultation services for a broad constituency, internally and externally.
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Identifying and supporting process improvements and supporting department projects.
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Working with minimal supervision, using comprehensive decision making skills and diverse procedures/policies requiring analytical and interpretive thinking to manage and develop Surveys products.
Specific Duties
Primary duties and responsibilities of the Technical Specialist I:
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Validate technical accuracy of Surveys and Quality Management programs through:
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critical oversight of creation of documents,
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critical review of analytical and statistical reports for accuracy and identification and reconciliation of any unexpected data
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consultation with committee members, material vendors and in vitro diagnostic companies to ensure information in program materials (ie, kit instructions, PSRs) are accurate
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integration of information from all contributing sources, and
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coordination of production schedules.
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Manage and ensure accuracy of databases/specifications result forms.
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Adhere to all established timelines for development and delivery of documents/materials related to assigned programs.
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Works with minimal supervision on assigned tasks and programs.
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Assist with providing orientation, direction, and ongoing management to committees in areas of:
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CAP policy, operational procedures, information routing, resources, responsibilities, and strategic planning.
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Work with committee members to solicit ideas for new programs or enhancements to current programs
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Assist with providing comprehensive consultative services to all internal groups impacted by the Surveys Programs.
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Responsibilities to these areas may include:
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- document/systems development and review,
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gather, manage, and interpret information from internal or external sources,
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respond to questions or problem solving as issues arise, and
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manage materials piloting.
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Participate in cross departmental projects and foster interdepartmental collaborations as assigned.
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Assist with providing excellent customer service and consultative services externally on an ongoing basis., + Identify operational improvements and efficiencies for Scores and other relevant technologies
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Maintain awareness of activities in the field of laboratory medicine in assigned disciplines and for regulatory and legislative processes in general.
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Support committee meeting preparation activities and contribute to meeting minutes and staff report.
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Other duties as assigned
Requirements
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Good judgment.
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Self-initiator.
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Excellent decision-making abilities.
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Excellent listening, verbal, written, and organizational skills.
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Excellent customer service
Professional:
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Able to prioritize.
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Able to bring teams to consensus.
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Able to communicate and apply technical information to a diverse audience.
Technical:
- Computer proficiency
Education / Experience
Education:
- Baccalaureate degree required.
Experience:
- A minimum of 3 years of clinical laboratory experience, quality assurance, or regulatory health care environment, in roles of increasing responsibility and scope.