Oncology Research Specialist Job at Advocate Health Care (Charlotte)

Clinical Practice Specialist, Inpatient Oncology

The Clinical Practice Specialist (CPS) is a member of the nursing leadership tea...

Location

United States , Boston

Salary:

129800.00 - 148400.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Master of Science in Nursing required
Clinical Nurse Specialist track is preferred
Current RN license in Massachusetts (compact licensure) language
3 years of oncology nursing experience and 3 years of oncology experience
Expertise in oncology nursing standards and evidence-based practice required
Oncology-specific certification required within 3 years of hire
Strong communication and interpersonal skills
Excellent organizational and time management abilities
Proficiency in educational technology and software
Ability to mentor and guide nursing staff effectively

Job Responsibility

Models excellence in nursing practice using scientific knowledge and advanced concepts in the assessment, diagnosis, planning, implementation and evaluation of actual or potential problems in the oncology patient population
Collaborates and consults with nurses and other to influence nursing practices and improve care outcomes within a patient population
A key stake holder and decision maker for the development, implementation and evaluation of standards of care, policies, guidelines, the introduction of new equipment, technology, and practices at the point of care and the integration of EBP into daily operational activities
Maintains expertise in ONS, ASCO, and other professional nursing standards and stays current on oncology evidence and changes in disease and treatment practices
Participates in local and national professional activities and organizations to promote the educational and professional growth of self and others within DFCI and the community
Provides content expertise as needed
Collaborates with Professional Development Specialist on curriculum development based on Learning Needs Assessment results
Contributes to the creation of an environment that stimulates continuous self-learning, positive group processes, reflective practice, and the empowerment of others
Models constructive and mutually respectful relationships with colleagues
Fosters an environment that is sensitive to the needs of diverse populations, including but not limited to culture, ethnicity, gender, and age

Fulltime

Revenue Cycle Management Specialist

Senior Accountant specializing in Revenue Cycle Management with solid background...

Location

United States , San Antonio

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Bachelor's degree in Accounting, Finance, or related field
CPA or Master's degree preferred
Minimum 5 years of accounting experience
At least 2 years in revenue cycle management within healthcare or clinical research environment
Strong background in oncology clinical trials including sponsor/grant billing, contract management, and regulatory compliance
Proven ability to work with large, complex datasets and clinical trial management systems
Advanced skills in Excel
Experience with ERP and CRM systems preferred
Excellent analytical, problem-solving, and communication skills

Job Responsibility

Oversee and manage all aspects of revenue cycle related to oncology clinical trial operations including billing, collections, accounts receivable, and reconciliation
Work closely with clinical research coordinators, principal investigators, sponsors, and finance teams to ensure timely and accurate setup and invoicing of clinical trial projects
Analyze revenue streams, grants, and contracts for compliance with regulatory standards and company policies
Monitor, report, and resolve billing discrepancies and reimbursement issues
Ensure revenue is properly recognized according to GAAP and healthcare accounting guidance
Prepare month-end and year-end closing activities for clinical trial revenue accounts
Conduct periodic audits of clinical trial revenue processes and identify process improvement opportunities
Support external and internal audits related to clinical research billing and revenue recognition
Maintain current knowledge of relevant regulations affecting oncology revenue cycle and clinical billing practices
Prepare and present financial reports, analysis, and forecasting related to clinical trial operations to leadership

What we offer

Medical, vision, dental, life and disability insurance
401(k) plan
Free online training

Clinical Oncology Consultant

We are seeking an enthusiastic Clinical Oncology Consultant to join a supportive...

Location

United Kingdom , Greater London

Salary:

109725.00 - 145478.00 GBP / Year

Remedium Partners

Expiration Date

Until further notice

Requirements

Complete GMC registration with License to Practice
Fellow of the Royal College of Radiologists (or equivalent)
Completion of higher specialist training in Clinical Oncology
Entry onto the Specialist Register (or expected within six months of interview)
Experienced in running radiotherapy and SACT services for a primary tumour site (e.g., Breast) and one additional tumour site
Ability to provide expert clinical opinion and take full, independent responsibility for patient care
Good communication skills
Willingness to teach junior medical staff and medical students
Participation in the trust’s teaching programme
Experience in clinical audit

Job Responsibility

Run outpatient clinics and manage patients receiving day-case cancer treatments
Support unplanned care for oncology patients with the acute oncology team
Take ownership of your own site-specific workload
Contribute to medical leadership, management, and innovation within oncology services
Support and train junior doctors and allied health professionals
Promote inter-disciplinary working within the department and across the hospital
Ensure standards of evidence-based clinical practice are applied
Participate in departmental and multidisciplinary clinical audit
Contribute to research and innovative practice within oncology

What we offer

Flexible Job Planning
We work with you to create a job plan that aligns with your interests, expertise, and ambitions, promoting a healthy work-life balance

Fulltime

Senior Clinical Research Associate II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

Turkey

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Must be fluent in English and in the native language(s) of the country they will work in
Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
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

Oversight of Monitoring Responsibilities and Study Conduct
Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client 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
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Clinical Practice Specialist, Inpatient Oncology

The Clinical Practice Specialist (CPS) is a member of the nursing leadership tea...

Location

United States , Boston

Salary:

129800.00 - 148400.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Master of Science in Nursing required
Clinical Nurse Specialist track is preferred
Current RN license in Massachusetts (compact licensure)
3 years of oncology nursing experience and 3 years of oncology experience
Expertise in oncology nursing standards and evidence-based practice required
Oncology-specific certification required within 3 years of hire
Strong communication and interpersonal skills
Excellent organizational and time management abilities
Proficiency in educational technology and software
Ability to mentor and guide nursing staff effectively

Job Responsibility

Models excellence in nursing practice using scientific knowledge and advanced concepts in the assessment, diagnosis, planning, implementation and evaluation of actual or potential problems in the oncology patient population
Collaborates and consults with nurses and others to influence nursing practices and improve care outcomes within a patient population
A key stake holder and decision maker for the development, implementation and evaluation of standards of care, policies, guidelines, the introduction of new equipment, technology, and practices at the point of care and the integration of EBP into daily operational activities
Maintains expertise in ONS, ASCO, and other professional nursing standards and stays current on oncology evidence and changes in disease and treatment practices
Participates in local and national professional activities and organizations to promote the educational and professional growth of self and others within DFCI and the community
Provides content expertise as needed
Collaborates with Professional Development Specialist on curriculum development based on Learning Needs Assessment results
Contributes to the creation of an environment that stimulates continuous self-learning, positive group processes, reflective practice, and the empowerment of others
Models constructive and mutually respectful relationships with colleagues
Fosters an environment that is sensitive to the needs of diverse populations, including but not limited to culture, ethnicity, gender, and age

Fulltime

Associate Research Specialist

The Associate Research Specialist, under supervision, conducts routine laborator...

Location

United States , Los Angeles

Salary:

43680.00 - 61953.00 USD / Year

Children's Hospital Los Angeles

Expiration Date

Until further notice

Requirements

Experience working in a laboratory environment required
Preferred 1+ years experience performing laboratory research
Bachelor’s degree or equivalent experience in a scientific field
Applicants must have completed their bachelor’s degree by their anticipated start date

Job Responsibility

Conducts routine laboratory research procedures
Follows protocol to perform experiments
Tabulates data and may assist with analysis
Performs routine equipment maintenance and orders supplies
May provide instruction to support personnel

What we offer

Competitive compensation package
Robust benefits program

Fulltime

Associate Research Specialist

The Associate Research Specialist, under supervision, conducts routine laborator...

Location

United States , Los Angeles

Salary:

43680.00 - 61953.00 USD / Year

Children's Hospital Los Angeles

Expiration Date

Until further notice

Requirements

Experience working in a laboratory environment required
Preferred 1+ years experience performing laboratory research
Bachelor’s degree or equivalent experience in a scientific field
Applicants must have completed their bachelor’s degree by their anticipated start date
Must be self-motivated and passionate about science
Able to carry out tasks independently with instructions
Able to troubleshoot with some assistance
Able to be a team player and be task oriented
Willingness to continue to build on knowledge and to learn perform literature review
Willingness to work with zebrafish and handle embryos with aseptic techniques

Job Responsibility

Conducts routine laboratory research procedures
Follows protocol to perform experiments
Tabulates data and may assist with analysis
Performs routine equipment maintenance and orders supplies
May provide instruction to support personnel

What we offer

Competitive compensation package
Robust benefits program

Fulltime

Professional Development Specialist, Inpatient Research Nursing

The Professional Development Specialist (PDS) is a member of the nursing leaders...

Location

United States , Boston

Salary:

113200.00 - 133800.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Bachelor of Science in Nursing (BSN) required
3 years of clinical nursing experience
1 year of oncology experience
Current RN license in Massachusetts and/or New Hampshire as job requires
Professional certification required (NPD-BC, Oncology-specific, or other relevant certification) within 3 years of hire
Strong communication and interpersonal skills
Excellent organizational and time management abilities
Proficiency in educational technology and software
Ability to mentor and guide nursing staff effectively
Expertise in evidence-based practices, competency models, and simulation standards

Job Responsibility

Demonstrates expertise in areas of oncology clinical practice
Supports nurses in the management of symptom distress related to cancer
Provides expertise in the assessment of patient and family learning needs
May provide direct patient care, consult with other nurses or clinical staff
Collaborates and consults with nurses and others to influence nursing practices
Demonstrates leadership skills through the coordination of education, training, and competency assessment
Participates in local and national professional activities
Designs competency models in collaboration with content experts
Develops and analyzes the Learning Needs Assessment
Monitors compliance related to mandatory staff education

Fulltime

Oncology Research Specialist

Advocate Health Care

Location:
United States , Charlotte

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 03, 2026

Expiration:
February 03, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Oncology Research Specialist

Clinical Practice Specialist, Inpatient Oncology

Revenue Cycle Management Specialist

Clinical Oncology Consultant

Senior Clinical Research Associate II - FSP

Clinical Practice Specialist, Inpatient Oncology

Associate Research Specialist

Associate Research Specialist

Professional Development Specialist, Inpatient Research Nursing

Oncology Research Specialist

Advocate Health Care

Location:United States , Charlotte

Category:Research and Development

Contract Type:Not provided

Salary:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:February 03, 2026

Expiration:February 03, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Oncology Research Specialist

Clinical Practice Specialist, Inpatient Oncology

Revenue Cycle Management Specialist

Clinical Oncology Consultant

Senior Clinical Research Associate II - FSP

Clinical Practice Specialist, Inpatient Oncology

Associate Research Specialist

Associate Research Specialist

Professional Development Specialist, Inpatient Research Nursing

Location:
United States , Charlotte

Category:
Research and Development

Contract Type:
Not provided

Job Posted:
February 03, 2026

Expiration:
February 03, 2026