Top 76 Oncology research Jobs in New York, Ny

Clinical Research Coordinator
Columbia University —New York, NY
- $64,350 - $65,000 a year
- Full-time
- Hybrid work
- Patient monitoring
- Mid-level
- Bachelor's degree
- Retirement plan
Clinical Research Coord I
Columbia University —New York, NY
- $66,300 - $72,000 a year
- Full-time
- HIPAA
- Mid-level
- Databases
Clinical Research Coordinator, Research Biofluid Management Unit; Monday-Friday, 11AM - 7PM * Oncology clinical research experience preferred *
NYU Langone Health —New York, NY
- $70,481.60 - $76,450.00 a year
- Monday to Friday
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Wellness program
Program Manager, Neuro-Oncology & Oncology Research - Manhattan Cancer Center
NYU Langone Health —New York, NY
- $70,481.60 - $121,580.64 a year
- Hospital
- Master's degree
- Administrative experience
- Wellness program
Clinical Research Associate, IQVIA Biotech
IQVIA —New York, NY
- $71,900 - $169,300 a year
- Full-time
- Bachelor's degree
- Travel
- Experience equivalent to degree accepted
Clinical Research Assistant
NYU Langone Health —New York, NY
- $53,294.21 - $55,000.00 a year
- Computer literacy
- Writing skills
- HIPAA
- Wellness program
10d
Data Coordinator I
Columbia University —Fort Lee, NJ
- $66,300 - $68,000 a year
- Full-time
- Hybrid work
- Computer literacy
- HIPAA
- Office
Clinical Research Associate (CRA) - Oncology (Remote)
Merck —Rahway, NJ
- $96,200 - $151,400 a year
- Full-time
- Remote
- English
- Mid-level
- Microsoft Office
- Paid holidays
- Health insurance
Research Assistant | Laboratory of Molecular Neuro-Oncology
Rockefeller University —New York, NY
- $50,000 - $55,000 a year
- Full-time
- Bachelor's degree
- Neurology
- Organizational skills
Clinical Research Coordinator * Oncology clinical research experience preferred *
NYU Langone Health —New York, NY
- $70,481.60 - $74,793.60 a year
- Online Application
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Wellness program
Assistant Research Scientist - AI-Linked Cytology (P.I.: Dr. John McDevitt)
New York University —New York, NY
- $55,000 - $65,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Databases
Assistant Clinical Research Manager
Columbia University —New York, NY
- $85,000 - $91,000 a year
- Full-time
- Hybrid work
- Mid-level
- University
- Bachelor's degree
CRA 1, IQVIA Biotech
IQVIA —New York, NY
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
Scientific Lead, Translational Sciences
Eli Lilly —New York, NY
- $166,500 - $266,200 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
- Dental insurance
16h
Expert In Vitro Biologist
Cogent Scientific —New York, NY
- $110,000 - $125,000 a year
- Full-time
- Doctor of Philosophy
- Senior level
- 4 years
- Paid holidays
- Health insurance
Quick Apply
10d
CRA 2/Senior CRA
IQVIA —New York, NY
- $90,200 - $175,100 a year
- Full-time
- Mid-level
- Bachelor's degree
- Experience equivalent to degree accepted
Theranostics & Research Coordinator
East River Medical Imaging, PC —New York, NY
- $28 - $32 an hour
- Full-time
- Hybrid work
- 5 years
- Mid-level
- Analysis skills
Quick Apply
FSP - Sr. CRAs & CRA 1/2 - Ophthalmology
Fortrea —New York, NY
- $110,000 - $145,000 a year
- Full-time
- Office
- Travel
- Ability to sit for extended periods
2d
Oncology Research Nurse I
Columbia University —New York, NY
- $115,000 - $125,000 a year
- Full-time
- Microsoft Word
- Nursing
- RN License
Sr. CRA 2, FSP - Oncology - East Coast
Fortrea —New York, NY
- $115,000 - $140,000 a year
- Full-time
- Mid-level
- Office
- Travel

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Clinical Research Coordinator

Columbia University -
New York, NY

Apply Now

Job Details

Full-time
$64,350 - $65,000 a year

Benefits

Retirement plan

Qualifications

FDA submissions
Direct patient care
Informed consent
Patient monitoring
Adverse event reporting
Clinical incident reports
Clinical research audit management
Filing
Mid-level
Project communication management
Investigational new drug (IND) applications
ECG equipment
Patient safety
Medical scheduling
Research project coordination
Clinical staff training
Bachelor's degree
Blood sample handling
Clinical training
Team training
Packaging
Informed consent procedures implementation
Implementing research protocols
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
Data collection
Research participation
Patient data collection
Patient treatment
Documentation Handling

Full Job Description

Job Type: Officer of Administration
Bargaining Unit:
Regular/Temporary: Regular
End Date if Temporary:
Hours Per Week: 35
Standard Work Schedule:
Building:
Salary Range: $64,350 - $65,000

The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting.

Position Summary

The Section of Oncology at Columbia University Medical Center is recruiting for the position of a Clinical Research Coordinator (CRC). The employee will work within the Division of Hematology, Oncology and Stem Cell Transplantation. The section of Oncology has a cadre of Phase 1 and 2 trials, investigator-initiated studies, and industry sponsored studies. The CRC will be assigned to studies based on need and review of clinical trial roster. The CRC will work with investigators, study staff, Scientific Review Committee (SRC) and institutional review boards (IRB), clinical trial sponsors and federal regulatory agencies to assure compliance with study protocols, data documentation, reporting requirements, ensure that regulatory requirements for clinical trials are met. The CRC will work under the supervision of the Section Head, Divisional Administrator and CTO Program Manager.

At CUIMC, we are leaders in teaching, research, and patient care and are proud of the service and support we provide to our community. We apply the same rigor in our commitment to fostering an inclusive, thriving community and caring for our employees and their loved ones. Columbia University offers a range of benefits to help you and your dependents stay healthy, build long-term financial security, meet educational and professional goals, and more. Explore your options for Health and Welfare, Employee Assistance, Tuition Programs, and Retirement Benefits.

“Subject to business needs, we may support flexible and hybrid work arrangements. Options will be discussed during the interview process”

Responsibilities

Schedule all protocol required evaluations (physical exams, radiology, labs, etc.)
Coordinate patient appointments with physicians, nurses and all test areas.
Attend Investigator meetings, which establish required procedures.
Coordinate, obtain, process (e.g. spin/separate/freeze samples), and ship (e.g. utilization of specific packaging and ensuring proper handling and shipping of samples) protocol required samples.
Obtain vital signs and EKGs as indicated.
Maintain accurate patient research files and records of sample procurement.
Develop protocol specific flow charts, intake sheets and other tools as needed to ensure protocol compliance and proper data acquisition.
Maintain study supplies and utilizes study specific supplies as required.
Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.
Assists Principal Investigator to assure that all key personnel or persons ‘engaged’ in the research project have met training requirements in accordance with federal regulations and university and sponsoring agency policies and procedures.
Cooperates with university compliance and monitoring efforts related to sponsored program administration and reports instances of noncompliance to the appropriate compliance office.
Coordinates and facilitates monitoring auditing visits and notifies appropriate institutional officials of external audits by FDA and sponsors.
Collaborates with PI and institution to respond to any audit findings and implement-approved recommendations.
Cooperates with university and sponsoring agency compliance and monitoring efforts related to human research participant protection and reports instances of noncompliance to the appropriate compliance office.
Establish and maintain regular communication with study team, study sponsor, and applicable regulatory agencies to ensure all required information is communicated.
Serve as facilitator for study team and sponsor with regard to study status information, safety issues, upcoming protocol amendments, consent changes, and applicable protocol training.
Prepares and submits all protocol applications, amendments, continuing reviews, and informed consent documents for SRC and IRB review and approval.
Prepares and submits regulatory documentation that may include IND/IDE applications, FDA annual reports, Serious Adverse Event reports, to the appropriate regulatory agencies including the Food and Drug Administration (FDA) etc.
Coordinates assigned study monitoring and auditing visits with study coordinator, investigator, industry sponsors, and internal/external auditors.
Performs related duties & responsibilities as assigned/requested.

Minimum Qualifications

Bachelor’s degree or equivalent and experience required.

Preferred Qualifications

Two years of related experience.
Protocol oversight; monitoring and reporting of study events; data collection; adherence to study protocols; in-service education of physicians, nurses, and support staff to protocol requirements; coordinate research activities.

Equal Opportunity Employer / Disability / Veteran

Columbia University is committed to the hiring of qualified local residents.

Apply Now

Refine Your Search

oncology research jobs in new york, ny

Clinical Research Coordinator

Clinical Research Coord I

Clinical Research Coordinator, Research Biofluid Management Unit; Monday-Friday, 11AM - 7PM * Oncology clinical research experience preferred *

Program Manager, Neuro-Oncology & Oncology Research - Manhattan Cancer Center

Clinical Research Associate, IQVIA Biotech

Clinical Research Assistant

Data Coordinator I

Clinical Research Associate (CRA) - Oncology (Remote)

Research Assistant | Laboratory of Molecular Neuro-Oncology

Clinical Research Coordinator * Oncology clinical research experience preferred *

Assistant Research Scientist - AI-Linked Cytology (P.I.: Dr. John McDevitt)

Assistant Clinical Research Manager

CRA 1, IQVIA Biotech

Scientific Lead, Translational Sciences

Expert In Vitro Biologist

CRA 2/Senior CRA

Theranostics & Research Coordinator

FSP - Sr. CRAs & CRA 1/2 - Ophthalmology

Oncology Research Nurse I

Sr. CRA 2, FSP - Oncology - East Coast

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