Principal Investigator Job at Randstad (Melbourne)

Principal Investigator, Federal Research Projects

We are seeking a Principal Investigator (PI) to support proposal development and...

Location

United States

Salary:

Not provided

DaqScribe Solutions

Expiration Date

Until further notice

Requirements

Strong background in embedded computing systems and real-time signal processing
Experience in Artificial Intelligence (AI) and Machine Learning (ML)
Proven leadership in conducting research projects and managing small teams
Skilled in data analysis and research methodologies
Excellent problem-solving and critical thinking abilities
Strong written and verbal communication skills
Ability to work independently and in a remote environment
Master’s or Ph.D. in Computer Science, Computer Engineering, Electrical Engineering, or a related technical field
U.S. citizenship is required
Must be able to obtain and obtain a security clearance at the Secret (S) and Top Secret (TS) levels

Job Responsibility

Lead proposal development for federal research opportunities in relevant topic areas or related domains
Manage and guide a multidisciplinary research team through concept, execution, and delivery
Design, implement, and evaluate novel signal processing and machine learning methodologies
Contribute to commercialization strategies stemming from federally sponsored R&D projects
Interface with government sponsors, collaborators, and internal teams throughout the research lifecycle
Participate in the “Technology Transfer” and commercialization process for all prototypes and technologies developed through government-funded research projects

Fulltime

New

Research Nurse

The clinical Research Nurse will provide direct patient care to patients enrolle...

Location

United States , Weymouth

Salary:

38.20 - 77.39 USD / Hour

South Shore Health

Expiration Date

April 05, 2026

Requirements

Graduate of an accredited School of Nursing as validated through the Massachusetts Board of Registration in Nursing
Baccalaureate degree in nursing strongly preferred. If associate degree in nursing, must complete BSN degree within 4 years
Minimum of 1-year recent experience as an RN
Ambulatory and/or oncology experience preferred
RN - Registered Nurse in Massachusetts
BLS - Basic Life Support.
ACLS - Advanced Cardiac Life Support accepted as minimum requirement
Professional nursing certification preferred (OCN, BMTCN, CPHON, AOCNP, CRNI, RN-BC)
Demonstrated flexibility and ability to work as an effective member of an interdisciplinary team.
Demonstrated skills in critical thinking, problem solving, and ability to make independent decisions.

Job Responsibility

Assists principal investigator with protocol development
Assists principal investigator as appropriate with the Institute’s protocol review process
Assists the principal investigator in developing the protocol budget
Collaborates with the Dana-Farber Harvard Cancer Center DFHCC quality assurance of clinical trials office in developing protocol specific materials
Serves as research coordinator for National Cancer Institute, pharmaceutical-sponsored, and National Cooperative Group protocols
Assists with recruitment and registration of patients to clinical trials
Coordinates scheduling of patient’s laboratory and radiographic assessments, admissions and clinic visits
Monitors test results as appropriate
Coordinates protocol data management as necessary
Collaborates with staff within the Institute and with outside organizations in the completion of clinical research trials

Fulltime

Clinical Research Nurse GYN

The Research Nurse in collaboration with the physician, is responsible for the i...

Location

United States , Boston

Salary:

42.65 - 105.81 USD / Hour

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Associate degree, Nursing
Baccalaureate degree in Nursing strongly preferred
If Associate degree in Nursing, must complete BSN degree within 4 years
1 year of recent experience as a Registered Nurse
Ambulatory and/or oncology experience preferred
Licensed as a Registered Nurse in the Commonwealth of Massachusetts, or State of New Hampshire as appropriate required
AHA BLS required (AHA ACLS accepted as minimum requirement)
Professional nursing certification preferred (OCN, BMTCN, CPHON, AOCNP, CRNI, RN-BC)

Job Responsibility

Assists principal investigator with protocol development
Assists principal investigator as appropriate with the Institute’s protocol review process
Assists the principal investigator in developing the protocol budget
Collaborates with the Dana-Farber Harvard Cancer Center DFHCC quality assurance of clinical trials office in developing protocol specific materials
Serves as research coordinator for National Cancer Institute, pharmaceutical-sponsored, and National Cooperative Group protocols
Assists with recruitment and registration of patients to clinical trials
Coordinates scheduling of patient’s laboratory and radiographic assessments, admissions and clinic visits
Monitors test results as appropriate
Coordinates protocol data management as necessary
Collaborates with staff within the Institute and with outside organizations in the completion of clinical research trials

Fulltime

Clinical Research Nurse Breast Oncology

The Research Nurse in collaboration with the physician, is responsible for the i...

Location

United States , Boston

Salary:

42.65 - 105.81 USD / Hour

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Licensed as a registered Nurse in the Commonwealth of Massachusetts, or State of New Hampshire as appropriate
Baccalaureate degree in nursing strongly preferred. If associate degree in nursing, must complete BSN degree within 4 years
Minimum of 1-year recent experience as an RN
Ambulatory and/or oncology experience preferred
Professional nursing certification preferred (OCN, BMTCN, CPHON, AOCNP, CRNI, RN-BC)
AHA BLS required (AHA ACLS accepted as minimum requirement)
Maintains BLS certification

Job Responsibility

Assists principal investigator with protocol development
Assists principal investigator as appropriate with the Institute’s protocol review process
Assists the principal investigator in developing the protocol budget
Collaborates with the Dana-Farber Harvard Cancer Center DFHCC quality assurance of clinical trials office in developing protocol specific materials
Serves as research coordinator for National Cancer Institute, pharmaceutical-sponsored, and National Cooperative Group protocols
Assists with recruitment and registration of patients to clinical trials
Coordinates scheduling of patient’s laboratory and radiographic assessments, admissions and clinic visits
Monitors test results as appropriate
Coordinates protocol data management as necessary
Collaborates with staff within the Institute and with outside organizations in the completion of clinical research trials

Fulltime

Oncology Research Nursing Professional

The Oncology Research Nursing Professional (ORNP) –is a Registered Nurse (RN) wh...

Location

United States of America , Palo Alto

Salary:

83.98 - 111.27 USD / Hour

Stanford Health Care

Expiration Date

Until further notice

Requirements

BSN or higher-level nursing degree required
5 plus years nursing experience required OR 3+ years in an oncology research nurse role required
2 or more years of experience in oncology
California Registered Nurse (RN) license
American Heart Association Basic Life Support (BLS) certification
Ability to communicate vetted information at all levels of the organization
Ability to be highly- and multi- task focused while managing multiple tasks and projects simultaneously across various platforms
Ability to understand information flow and solve problems under pressure
Ability to manage conflict resolution
Ability to adapt and troubleshoot in a unique and quickly changing, fast-paced environment

Job Responsibility

Collaborates with the investigator and serves as lead on study patient screening, eligibility determination and enrollment assessments on assigned clinical trials
Uses independent judgement to assess, identify, and prioritize clinical information to physician, NP, PA and other clinicians for patients who are being evaluated and/or enrolled in a clinical trial
Assesses and documents signs and symptoms of illness, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the research protocol
Manage patient/family phone calls – collaborating with MD, NP and/or PA as needed to obtain orders for the management of the patient
Manages and communicates all aspects of care as defined by the research protocol with the physician and other health care professionals and research team members
Collaborates with CRC to assure that therapeutic clinical trial flag is placed on the patient during active treatment
Plans, coordinates, and completes randomization (if applicable), patient assessments (toxicity assessment, diagnostic tests, and questionnaires), treatments and follow up care according to the defined protocol treatment plan
Manages the consent process to ensure it is performed in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations
Oversees and participates in the education of the patient regarding the clinical trial
Alerts principal investigator of any concerns raised by the patient during the informed consent process

Fulltime

New

Research Audiologist

The Research Audiologist will assist in development of research protocols, manag...

Location

United States , Fayetteville

Salary:

85000.00 - 91000.00 USD / Year

THE GENEVA FOUNDATION

Expiration Date

Until further notice

Requirements

U.S. Citizen, able to pass security/background checks for access to restricted Federal facilities
Ph.D. or Au.D. required
3-5 years knowledge and experience with Department of War (DoW) Grants and agreements administration and management, preferred
3-5 years medical research project management experience strongly desired, preferably with Department of War and Special Operations populations
Experience with advanced medical technologies, preferred
Knowledge of military system, preferred
Demonstrate competence in oral and written communication
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
Ability to be flexible with changing priorities and available to interact with employees, clients and sponsors of all levels
Ability to exercise independent judgment in fast-paced, high-pressured environment with strict deadlines and to manage multiple projects

Job Responsibility

Assists in the development of the research protocol(s) as the subject matter expert
Reviews research documentation and provides detailed technical written notes
Directs and performs recurring analyses on research portfolios to identify critical gaps, exceptional results and/or lack of progress
Manages and organizes data and assure that necessary archival procedures have been conducted
Interacts with other services and government agencies, organizes and hosts research planning and coordination meetings, and informs the Principal Investigator of developments
Maintains open communication with the Principal Investigator, advise of processes, report progress and serve as a point of contact, as applicable
Provides guidance to scientists preparing research proposals and abstracts/posters/manuscripts, to include guidance on research protocol development, as needed
Performs scientific reviews on research proposals submitted for consideration, as requested
Maintains and updates files of all applicable regulatory documentation for IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.)

What we offer

medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution
Coverage is provided for employees and family members including domestic partners
Short-and long-term disability
Employee Assistance Program
Life & ADD insurance
403b retirement plan with generous employer match
flexible leave options
11 paid holidays per year

Fulltime

New

Research Psychologist/Neuropsychologist

The Research Psychologist/Neuropsychologist will assist in development of resear...

Location

United States , Fort Bragg

Salary:

90000.00 - 105000.00 USD / Year

THE GENEVA FOUNDATION

Expiration Date

Until further notice

Requirements

U.S. Citizen, able to pass security/background checks for access to restricted Federal facilities
Doctoral degree (PhD or PsyD) in Psychology, Neuropsychology, or a closely related field required
3-5 years knowledge and experience with Department of War (DoW) Grants and agreements administration and management, preferred
3-5 years medical research project management experience strongly desired, preferably with Department of War and Special Operations populations
Experience with advanced medical technologies, preferred
Demonstrate competence in oral and written communication
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
Ability to be flexible with changing priorities and available to interact with employees, clients and sponsors of all levels
Ability to exercise independent judgement in fast-paced, high-pressured environment with strict deadlines to manage multiple projects
Ability to develop strong trusting relationships in order to gain support and achieve results

Job Responsibility

Assists in the development of the research protocol(s) as the subject matter expert
Reviews research documentation and provides detailed technical written notes
Directs and performs recurring analyses on research portfolios to identify critical gaps, exceptional results and/or lack of progress
Manages and organizes data and assure that necessary archival procedures have been conducted
Interacts with other services and government agencies, organizes and hosts research planning and coordination meetings, and informs the Principal Investigator of developments
Maintains open communication with the Principal Investigator, advise of processes, report progress and serve as a point of contact, as applicable
Provides guidance to scientists preparing research proposals and abstracts/posters/manuscripts, to include guidance on research protocol development, as needed
Performs scientific reviews on research proposals submitted for consideration, as requested
Maintains and updates files of all applicable regulatory documentation for IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.)
Collect neurocognitive, psychological, and other relevant clinical data using standardized assessment tools and research protocols

What we offer

medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution
Coverage is provided for employees and family members including domestic partners
Short-and long-term disability
Employee Assistance Program
Life & ADD insurance
403b retirement plan with generous employer match
flexible leave options
11 paid holidays per year

Fulltime

Senior Clinical Research Coordinator

The Computational Health Informatics Program (CHIP) is seeking an experienced, h...

Location

United States , Boston

Salary:

58676.80 - 93901.60 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Bachelor’s degree
Master’s preferred
Bachelor’s degree and 4 years of relevant work experience OR Master’s degree and 2 years of relevant work experience
Analytical skills to gather and interpret data in which the information or problems are moderately complex to complex
Well-developed communication skills to provide critical information to patients, effectively deal with conflicting views or issues, and the ability to mediate fair solutions
Ability to effectively engage with and influence others
build working relationships and can work independently and as a team member, leads others when needed
Act as a resource and must be knowledgeable and compliant in all hospital, State, and Federal regulatory requirements, including hospital policy and procedures

Job Responsibility

In conjunction with the Principal Investigator and/or designees designs, develops, and implement clinical research projects such as enrollment strategies, study materials, and study documents
Responsible for daily operations of the study
Develops and implements processes and procedures to meet study goals and protocol requirements
Participate in training and prepare study related training materials
Plans and prioritizes the work of administrative and support personnel on all clinical study activities
Consents and enrolls patients for research studies by providing detailed information on the Clinical Study to patients and families
Communicates all policies and procedures and responds to all inquiries
Evaluate the suitability of prospective study candidates and make selections based on clinical knowledge of each study
Provide input for updates of SOPs and drafting of new quality documentation
Assist with developing and implementing best practice guidelines for conducting various clinical research protocols

What we offer

flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

Principal Investigator

Randstad

Location:
Australia , Melbourne

Category:
-

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 26, 2026

Expiration:
March 15, 2026

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