CrawlJobs Logo
Abridge Logo Abridge · IT - Software Development

Nurse Scientist

United States, San Francisco 221000.00 - 260000.00 USD / Year · Job Posted January 20, 2026
Apply Position
Job Link Share

Job Description

Abridge is seeking a Nurse Scientist to drive the development of our AI-powered nursing documentation tools. The ideal candidate is a current/former Practicing Nurse with a strong background in Nursing Informatics and technical expertise, blending clinical knowledge with experience using informatics to drive the development of new technologies. In this role, you will help shape AI-driven documentation tools, ensuring our models generate accurate, high-quality nursing notes that enhance nurses’ efficiency and patient care. You’ll work closely with engineers, researchers, and other clinicians to refine AI models, validate outputs, and develop new capabilities that improve documentation workflows. This is a high-impact opportunity to be a part of developing the product that will help nurses concentrate on what matters most– connecting with patients and delivering exceptional care.

Job Responsibility

  • Develop and refine AI-driven nursing documentation tools using clinical expertise and collaborating with prompt engineers.
  • Design experiments to assess and validate the accuracy of AI-generated nursing documentation and provide structured feedback.
  • Build and refine evaluation tools to streamline nursing documentation quality assessment.
  • Collaborate with cross-functional teams (ML researchers, data scientists, clinicians) to integrate nursing insights into AI models.
  • Contribute to product development and broader business initiatives.

Requirements

  • RN, or PhD with direct experience working in nursing practice
  • Deep understanding of nursing documentation, nursing workflows, and nursing terminology
  • Ability to evaluate AI-generated clinical notes using a data-driven approach, provide structured feedback, and guide improvements
  • Hands-on experience in clinical data validation and quality assessment.
  • Strong knowledge of healthcare data standards (e.g., FHIR, HL7) and privacy regulations (e.g., HIPAA)
  • Experience collaborating with engineers and product teams to build AI-powered clinical tools
  • Strong analytical and problem-solving skills
  • Excellent written and verbal communication skills

Nice to have

  • Experience in software engineering, particularly in prompt engineering or AI model development
  • Previous experience in AI-powered clinical documentation tools or clinical decision support systems
  • Published research in AI, machine learning, or healthcare technology

What we offer

  • Generous Time Off: 14 paid holidays, flexible PTO for salaried employees, and accrued time off for hourly employees
  • Comprehensive Health Plans: Medical, Dental, and Vision coverage for all full-time employees and their families.
  • Generous HSA Contribution: If you choose a High Deductible Health Plan, Abridge makes monthly contributions to your HSA.
  • Paid Parental Leave: Generous paid parental leave for all full-time employees.
  • Family Forming Benefits: Resources and financial support to help you build your family.
  • 401(k) Matching: Contribution matching to help invest in your future.
  • Personal Device Allowance: Tax free funds for personal device usage.
  • Pre-tax Benefits: Access to Flexible Spending Accounts (FSA) and Commuter Benefits.
  • Lifestyle Wallet: Monthly contributions for fitness, professional development, coworking, and more.
  • Mental Health Support: Dedicated access to therapy and coaching to help you reach your goals.
  • Sabbatical Leave: Paid Sabbatical Leave after 5 years of employment.
  • Compensation and Equity: Competitive compensation and equity grants for full time employees.
Abridge - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Nurse Scientist

8 matching positions

New

Senior Clinical Research Associate/Clinical Research Associate II - Oncology

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
United States
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) in a CRO or pharma organization
  • Preferred therapeutic experience in Oncology
  • Global clinical trial experience preferred
  • Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
  • Must be fluent in English and in the native language(s) of the country they will work in
  • Travel (60-80%) within area is required
  • Valid driver’s license and passport required
  • Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
  • Demonstrated knowledge of global and local regulatory requirements
  • Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Job Responsibility
Job Responsibility
  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and sponsor standards to achieve project goals, timelines and quality
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
  • During study conduct, serve as the primary point of contact for assigned investigator sites
  • Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
  • Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
  • Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
  • Provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
  • Attend investigator meeting when required (virtual or F2F)
  • Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators
  • Partner with SCP and the study team to define and support recruitment initiatives at site level
What we offer
What we offer
  • Flexible work arrangements
  • Career growth and development
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
  • Fulltime
Read More
Arrow Right

Medical Lab Specialist II

Baptist Health is currently looking for a Medical Laboratory Scientist II to joi...
Location
Location
United States , Jacksonville
Salary
Salary:
Not provided
baptistjax.com Logo
Baptist Health (Florida)
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 2 years Medical Technologist Experience
  • Associate of Science Required
  • Bachelor of Science (non-Nursing) Preferred
  • Certified Medical Technologist (MT) Preferred Or
  • Certified Medical Laboratory Technician (MLT) Preferred Or
  • Licensed Medical Technologist Required Or
  • Licensed Clinical Laboratory Technician Required Or
  • Candidates licensed prior to 1997 are not required to have certification per the State of Florida Licensure rules
Job Responsibility
Job Responsibility
  • Maintaining expertise and performing technical, specimen collection/processing, LIS, general department, and clerical functions in one or more laboratory sections
  • Maintaining records of performance as defined in the laboratory's general and sectional policy and procedure manuals
  • Maintaining records of performance as defined in the SOP manuals
  • Instructing new employees and students
  • Supervising MLTs as General Supervisor and serve as Charge Technologist in the absence of other lab supervisors or MTs
  • Working with Director and Section Supervisors, however, the candidate can perform all responsibilities of this job description without on-site supervision
What we offer
What we offer
  • Relocation Assistance Available
  • Fulltime
Read More
Arrow Right

Medical Lab Scientist II, Evenings, Baptist Silverleaf

Baptist Health is currently looking for a Medical Laboratory Scientist II to joi...
Location
Location
United States , Jacksonville
Salary
Salary:
Not provided
baptistjax.com Logo
Baptist Health (Florida)
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 2 years Medical Technologist Experience
  • Associate of Science Required
  • Bachelor of Science (non-Nursing) Preferred
  • Certified Medical Technologist (MT) Preferred
  • Certified Medical Laboratory Technician (MLT) Preferred
  • Licensed Medical Technologist Required
  • Licensed Clinical Laboratory Technician Required
Job Responsibility
Job Responsibility
  • Maintaining expertise and performing technical, specimen collection/processing, LIS, general department, and clerical functions in one or more laboratory sections
  • Maintaining records of performance as defined in the laboratory's general and sectional policy and procedure manuals
  • Maintaining records of performance as defined in the SOP manuals
  • Instructing new employees and students
  • Supervising MLTs as General Supervisor and serve as Charge Technologist in the absence of other lab supervisors or MTs
  • Working with Director and Section Supervisors, however, the candidate can perform all responsibilities of this job description without on-site supervision
What we offer
What we offer
  • Relocation Assistance Available
  • Fulltime
Read More
Arrow Right

Assistant Laboratory Supervisor

The Assistant Supervisor is responsible for performing, evaluating, and reportin...
Location
Location
United States , Hollywood
Salary
Salary:
Not provided
mhs.net Logo
Memorial Healthcare System
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Accredited Program
  • Clinical Lab Supervisor License (SU LICENSE) - State of Florida (FL)
  • Five (5) years of experience as a Clinical Laboratory Technologist
  • Graduate of an accredited Medical Technologist, Medical Laboratory Scientist program, or accredited Histotechnology program
Job Responsibility
Job Responsibility
  • Reviews and troubleshoots quality control and equipment issues
  • Observes and instructs student technologists and new or current employees
  • Effectively manages resources such as productivity, supplies, instruments and equipment
  • Plans work and completes job responsibilities in an efficient and productive manner
  • Reports test results in a timely manner according to established laboratory protocols
  • May provide supervision of a laboratory section
  • May perform method validations and ongoing method assessments
  • Effectively communicates with nursing and medical staff
  • Ensures staff compliance with regulatory, departmental and organizational policies, procedures and protocols
  • Assists or provides monitoring and coaching of team members and provides input in the evaluation of team members performance
What we offer
What we offer
  • $20K Sign on Bonus
  • Fulltime
Read More
Arrow Right

Clinical Research Coordinator II - Precision Medicine

A Clinical Research Coordinator II (CRC II) position is available for the Precis...
Location
Location
United States , BOSTON
Salary
Salary:
56000.00 - 63700.00 USD / Year
dana-farber.org Logo
Dana-Farber Cancer Institute
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • bachelor's degree or 2 years of experience as a Dana-Farber Clinical Research Coordinator
  • 1-3 years of relevant experience
  • preference for those with a background in medical or scientific research or a technology-oriented business environment
  • excellent organization and communications skills
  • strong interpersonal skills
  • detail oriented
  • ability to effectively manage time and prioritize workload
  • must practice discretion and adhere to hospital confidentiality guidelines
  • computer skills including the use of Microsoft Office
Job Responsibility
Job Responsibility
  • liaise between the LSP, DF/HCC hospitals, and external investigators to facilitate highly collaborative translational biomarker driven research
  • facilitate the emerging fields of cancer spatial biology
  • work closely with principal investigators, program managers, biomarker researchers, and data scientists
  • primary data collection and management of patient clinical information as it pertains to participation in clinical trials and patient consent
  • ensure timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities
  • support and maintain participant/subject trial binders and maintain regulatory binders
  • ensure study compliance with all state, federal, and IRB requirements
  • screen patients for protocol eligibility
  • obtain informed consent for non-treatment trials
  • register study participants with the clinical trials management system, ONCORE
  • Fulltime
Read More
Arrow Right

Clinical Lab Scientist

As our Clinical Lab Scientist at Memorial Hospital, you will help solve mysterie...
Location
Location
United States , Bakersfield
Salary
Salary:
56.36 - 66.39 USD / Hour
americannursingcare.com Logo
American Nursing Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • CA CLS
  • Education level necessary to obtain required licensure and certifications
  • One year acute care hospital experience preferred
  • Above average communication and organizational skills
  • Ability to adapt to workload demands and function efficiently during difficult or emergency situations
  • Ability to maintain and operate laboratory equipment
  • Must have medical terminology, basic computer terminology and data entry skills
Job Responsibility
Job Responsibility
  • Perform a variety of technical analyses, verify results and assure quality and accuracy of tests
  • Interact with physician, nurses, ward clerks, phlebotomists, other clinical laboratory scientists and other health care professionals in the resolution of problems involving patient specimen collection and handling, appropriateness of specimens, clarification of orders and result reporting
  • Consult with Clinical Laboratory Scientists, Laboratory Supervisors, Administrative Director of Laboratory Services, Medical Director of Laboratory Services, or Pathologists for policy clarification and problem resolution
  • Operate lab computer system according to manuals in each department
  • Maintain familiarity and compliance with general laboratory safety practices, MSDS guidelines, State of California regulations and requirements, OSHA standards, CDC recommendation and universal precautions
  • Participate in the clinical laboratory scientist teaching program to assist in the training of Clinical Laboratory Scientist students, MLT students, or other established programs
  • Perform other related duties as assigned
What we offer
What we offer
  • medical
  • prescription drug
  • dental
  • vision plans
  • life insurance
  • paid time off (full-time benefit eligible team members may receive a minimum of 14 paid time off days, including holidays annually)
  • tuition reimbursement
  • retirement plan benefit(s) including, but not limited to, 401(k), 403(b), and other defined benefits offerings
  • Fulltime
Read More
Arrow Right

Clinical & Medical Affairs Lead – Women’s Health

Do you want to help build the clinical and scientific foundation for a new categ...
Location
Location
Denmark , Copenhagen
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • MSc, PhD, MD, midwife, nurse-scientist, clinical researcher, or equivalent background in a relevant health/science field
  • Experience with clinical research, medical writing, clinical evidence, or medical affairs
  • Proven track-record in scientific writing
  • Familiarity with women’s health, maternal health, obstetrics, gynecology, midwifery, or postpartum care
  • Ability to engage clinical stakeholders and translate evidence into clear internal and external communication
  • Excellent English communication skills both verbally and in writing
Job Responsibility
Job Responsibility
  • Formulate oasicare’s clinical strategy in cooperation with management
  • Execute and own oasicare’s clinical strategy
  • Build oasicare’s internal clinical knowledge bank on women’s afterbirth/postpartum care, including existing literature, clinical claims, stakeholder questions, terminology, and scientific rationale
  • Own, produce and disseminate scientific publications: manuscripts, abstracts, posters, conference presentations, white papers, and peer-reviewed publications
  • Collaborate with commercial and marketing teams to create clinically credible materials for hospitals, OB/GYNs, midwives, partners, investors, and other stakeholders
  • Support the development and implementation of strategic education and training plans for internal and external stakeholders
  • Assist with the execution and ongoing support of clinical research studies and scientific initiatives
  • Act as a scientific authority and engage in high-quality scientific exchange in OB/GYNs, gynecologists, midwives, clinical investigators, and other women’s health stakeholders
  • Collaborate with R&D, regulatory, and QA teams to translate clinical insights into product development, evidence generation, clinical claims, and scientific rationale
  • Fulltime
Read More
Arrow Right

Director Nursing Research

Provides strategic leadership in the development and implementation of the depar...
Location
Location
United States , Milwaukee
Salary
Salary:
Not provided
childrenswi.org Logo
Children's Wisconsin
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • License RN-Registered Nurse (30) - State of Wisconsin required
  • Terminal Degree (PhD, DNP, etc.) required
  • Ten or more years of experience conducting clinically relevant research and publishing relevant findings
  • Academic and professional expertise in pediatric nursing preferred
  • Ability to communicate effectively with all members of the interdisciplinary health care team to enhance collaboration and problem solving
  • High degree of resourcefulness and independent motivation
  • Demonstrated ability to relate well with colleagues and community agencies
Job Responsibility
Job Responsibility
  • Provides strategic leadership in the development and implementation of the department of Nursing Research and Evidence-Based Practice
  • Provides vision and leadership for development of an agenda encompassing interdisciplinary research, evidence-based practice (EBP), nursing outcome datasets, and Magnet re-designation
  • Provides leadership for programs of research within the department as well as conducting own program of research
  • Facilitates research utilization in clinical practice and research consultation/collaboration with nurses and interdisciplinary colleagues
  • Defines needed infrastructure which to supports and directs nursing and interdisciplinary EBP and research activities
  • Develops a system and support for engaging and mentoring nurse scientists, Advanced Practice Nurses and clinical staff
  • The translation of clinically relevant research into clinical practice are key components of this role
  • Reports to the Vice President for Nursing/Chief Nursing Officer
  • Fulltime
Read More
Arrow Right