Clinical Research Nurse Breast Oncology Job at Dana-Farber Cancer Institute (Chestnut Hill)

Clinical Nurse Specialist – Breast Health

The Clinical Nurse Specialist (CNS) is an integral member of the Blackrock Healt...

Location

Ireland

Salary:

Not provided

Blackrock Health Hermitage Clinic

Expiration Date

Until further notice

Requirements

Registered in the general division of the Register of Nurses maintained by NMBI
At least five years recent post-registration nursing experience (full-time or equivalent hours part-time) in an acute hospital setting
Oncology/ Surgical Experience
A recognised level 8 post-registration Quality and Qualifications Ireland (QQI), National Framework of Qualifications (NFQ) major academic award relevant to the specialist area – Oncology Nursing/ Breast Care or Gynaecology, or be willing to complete same within one year of taking up post
Holds an up-to-date ACLS course or be in pursuit of same.

Job Responsibility

Assess and manage patients with breast cancer, benign breast disease, and other related conditions, ensuring the best possible clinical outcomes
Develop personalized care plans, integrating physical, emotional, and psychological aspects of care
Provide direct clinical care, including pre-operative, intra-operative, and post-operative care
Monitor patients throughout their treatment journey, adjusting care plans as necessary based on individual needs
Act as a point of contact for patient concerns and queries, providing guidance and emotional support
Ensure all patients receive necessary information to make informed decisions about their care, including options such as breast reconstruction and other available treatments, empowering them to make choices that align with their needs and values
Ensure that all patient records are kept accurate, legible, and up to date
Educate patients and families about breast health, treatment options, and side-effect management related to breast cancer and other breast conditions
Lead and facilitate breast care education programs and support groups for patients and their families
Provide counselling and emotional support for patients dealing with breast cancer diagnoses, treatment challenges, and survivorship

What we offer

Competitive salary
Onsite parking
Pension
Annual bonus*
Discounted café
Sports and Social club
Employee Assistance Programme
Discounted onsite pharmacy

Fulltime

Clinical Research Coordinator - Breast Oncology

The Clinical Research Coordinator (CRC) will work within the Breast Oncology cli...

Location

United States , Boston

Salary:

48100.00 - 54400.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Excellent organization and communications skills required
Strong interpersonal skills – ability to effectively interact with all levels of staff and external contacts
Must be detail oriented and have the ability to follow-through
Ability to effectively manage time and prioritize workload
Must practice discretion and adhere to hospital confidentiality guidelines at all times
Must have computer skills including the use of Microsoft Office
Bachelor’s Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience required
0-1 years of experience working in a medical or scientific research setting or comparable technology orientated business environment preferred

Job Responsibility

Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities
Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing, and archiving of study records, and resolution of data queries
May prepare and or complete regulatory related reports and IRB submissions
Maintain and organize study participant/subject trial binder and regulatory binders, enter all required study data on an ongoing basis and as applicable
Ensure all study related samples are collected, properly prepared, and shipped according to the protocol requirements and IATA/DOT regulations
Collaborate with other departments such as Protocol Scheduling, Materials Management, the Clinical Research Laboratory, Pharmacy, Research Nursing, and other departments, as needed per the requirements of the clinical trial
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits
Coordination and management of clinical trials throughout the trial life cycle, including communication with sponsors and regulatory authorities
Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved
Interact with study participants as directed/required by the protocol and/or study team

Fulltime

Clinical Research Coordinator - Breast Oncology Cohort Studies Program

The CRC (Clinical Research Coordinators) work within the clinical research progr...

Location

United States , Boston

Salary:

48100.00 - 54400.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Excellent organization and communications skills required
Strong interpersonal skills – ability to effectively interact with all levels of staff and externals contacts
Must be detail oriented and have the ability to follow-through
Ability to effectively manage time and prioritize workload
Must practice discretion and adhere to hospital confidentiality guidelines at all times
Must have computer skills including the use of Microsoft Office
Bachelor’s Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience required
0-1 years of experience working in a medical or scientific research setting or comparable technology orientated business environment preferred

Job Responsibility

Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities
Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing, and archiving of study records, and resolution of data queries
May prepare and or complete regulatory related reports and IRB submissions
Maintain and organize study participant/subject trial binder and regulatory binders, enter all required study data on an ongoing basis and as applicable
Ensure all study related samples are collected, properly prepared, and shipped according to the protocol requirements and IATA/DOT regulations
Collaborate with other departments such as Protocol Scheduling, Materials Management, the Clinical Research Laboratory, Pharmacy, Research Nursing, and other departments, as needed per the requirements of the clinical trial
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits
Coordination and management of clinical trials throughout the trial life cycle, including communication with sponsors and regulatory authorities
Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved
Interact with study participants as directed/required by the protocol and/or study team

Fulltime

Oncology Nurse Navigator 2 - Breast Oncology

The Oncology Nurse Navigator 2 is a registered nurse (RN) who works with physici...

Location

United States , Chicago

Salary:

84760.00 - 151715.20 USD / Year

IntelyCare

Expiration Date

Until further notice

Requirements

Current State of Illinois Registered Nurse licensure required
At least one year of nursing experience
Earned nursing degree of baccalaureate level of education or higher
Oncology nursing experience preferred
Oncology nursing certification preferred
Ability to travel throughout the Medical Center and some roles may require travel to other sites of care.

Job Responsibility

Establishes a caring therapeutic relationship with patients and families utilizing effective communication while managing a defined patient caseload
Assesses patients for social determinants of health
utilizing findings to develop a plan of care and mutual goal setting
Serves as liaison for the patient, becoming an expert on the patient and their needs throughout the trajectory of their care from diagnosis to end of life or survivorship
Advocates for patient and their families to ensure timely access to treatment and equal access to health care
Collaborates with all members of the health care team in a positive, professional manner to ensure coordination of patient care
Serves as a reference regarding clinical trials and coordinates care with The clinical trial office
Provides psycho-social support and Facilitates referrals and transitions of care ensuring effective utilization of internal and community resources
Provides symptom managements utilizing guidelines/evidence based practice from oncology resources in collaboration with providers
Performs role utilizing EBP within specialty established by nationally recognized oncology nursing associations, cancer societies and networks as well as published research and quality documents

Fulltime

Breast Medical Oncologist

An excellent opportunity has arisen to appoint a Consultant Breast Medical Oncol...

Location

United Kingdom , Greater London

Salary:

109725.00 - 145478.00 GBP / Year

Remedium Partners

Expiration Date

Until further notice

Requirements

Complete GMC registration with a licence to practise
MRCP or equivalent
Minimum 1 year of NHS experience
Specialist competence in Medical Oncology with a focus on breast cancer
Ability to work effectively within a multidisciplinary team
Strong communication, leadership, and organisational skills
Commitment to clinical governance, audit, and service improvement

Job Responsibility

Provide specialist Medical Oncology care for patients with breast cancer, including outpatient clinics, systemic therapy management, and follow-up care
Maintain continuous clinical responsibility for patients under your care
Actively participate in weekly multidisciplinary team (MDT) meetings
Support the Acute Oncology service, including advice for emergency oncology admissions
Provide on-site clinical support to chemotherapy services and the clinical trials unit, including review of chemotherapy prescriptions and patient assessment
Ensure patients are fully involved in decisions about their care, maintaining excellent communication with patients and families
Participate fully in clinical governance, audit, risk management, and patient safety activities
Contribute required data to audit programmes and quality assurance processes
Support compliance with NICE guidance, national cancer standards, and benchmarking requirements
Participate in incident reporting, Duty of Candour, and risk register processes

Fulltime

Breast Oncologist

An excellent opportunity has arisen for a Consultant Medical Oncologist to join ...

Location

United Kingdom

Salary:

109725.00 - 145478.00 GBP / Year

Remedium Partners

Expiration Date

Until further notice

Requirements

Medical Degree (MBBS or equivalent)
Full GMC registration with a licence to practise
MRCP or equivalent qualification
Entry on the GMC Specialist Register in Medical Oncology (or within 6 months of CCT / CESR)
Minimum 1 year NHS experience
Experience in General Medical Oncology
Subspecialty experience in: Breast malignancies
Testicular and renal cancers
Experience delivering systemic anti-cancer therapy (SACT)
Evidence of clinical audit participation

Job Responsibility

Provide Consultant-level care in Medical Oncology, particularly: Breast malignancies (primary focus)
Testicular and renal cancers
Deliver systemic anti-cancer therapy (SACT) including: New patient assessment
Treatment planning
Review and follow-up clinics
Manage patients across outpatient clinics, MDT pathways, and inpatient care
Undertake oncology ward rounds and acute oncology input
Attend and contribute to weekly MDT meetings (Breast, Urology, and related tumour groups)
Work closely with: Oncology consultants
Specialist nurses

Fulltime

Surgical Oncologist - Breast Surgeon

The Breast Surgical Oncologist is responsible for providing comprehensive, patie...

Location

United States , Rehoboth, Delaware

Salary:

624000.00 USD / Year

beebe healthcare

Expiration Date

Until further notice

Requirements

MD or DO degree from an accredited institution
Board Certified or Board Eligible in General Surgery
Fellowship training in Breast Surgical Oncology or Surgical Oncology with extensive breast experience (SSO-approved fellowship preferred)
Eligible for medical licensure in the state
Demonstrated expertise in breast cancer surgery and current knowledge of evidence‑based treatment guidelines

Job Responsibility

Provide expert surgical management for breast cancer and other breast diseases, including lumpectomy, mastectomy, sentinel lymph node biopsy, axillary surgery, reconstruction coordination, and risk-reducing procedures
Perform pre-operative evaluation, risk assessment, counseling, and follow-up care
Collaborate in multidisciplinary patient management with radiology, pathology, medical oncology, radiation oncology, genetics, navigation, and supportive services
Participate in multidisciplinary tumor board discussions and contribute to evidence‑based treatment planning
Ensure adherence to national standards of breast cancer care, including NCCN, NAPBC, ASCO, and Commission on Cancer guidelines
Capacity to perform stereotactic and ultrasound biopsy
Support the development and continuous improvement of the Breast Program and related oncology service lines
Contribute to achieving and maintaining accreditation standards (e.g., NAPBC, CoC)
Participate in clinical quality initiatives, outcomes monitoring, and process improvement projects
Engage in clinical research, clinical trials, retrospective studies, or quality-based research initiatives when applicable

Fulltime

Senior Clinical Research Associate

Senior Clinical Research Associate - Home based - France. ICON plc is a world-le...

Location

France , Paris

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Advanced degree in a relevant field such as life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license
Phase I Oncology Expertise: Strong background in early-phase oncology trials, including safety, PK/PD, and dose-escalation studies
Indication-Specific Knowledge: Experience with breast, ovarian, prostate, and pancreatic cancer clinical trials
Traditional Monitoring Model: Solid skills and proficiency in on-site monitoring, full source data verification, IP accountability and regulatory compliance
Trip Report Writing: Proven ability to produce detailed, accurate, and timely monitoring visit reports. Extensive experience working with a CTMS platform (Siebel CTMS, Veeva Vault CTMS, Medidata CTMS, Oracle Clinical/Clinical One, or others)

Job Responsibility

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fulltime

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Clinical Research Nurse Breast Oncology

Job Description

Job Responsibility

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