oncology research rn

Palomar Health

<div><div><div>Posting Date: 04/06/2026</div><div>
Internal Closing Date: 04/10/2026</div><ul><li>Internal candidates must apply by midnight on the Closing Date in order to have bidding rights.</li></ul><div>
</div></div><div>
Primarily responsible for the delivery of coordinated nursing care for a patient or an assigned group of patients within an assigned unit and for the day-to-day management and supervision of the related clinical activities. Coordinates plan of care with the client, their family and the interdisciplinary team. Also responsible for supervising and responsibly directing the activities of various levels of assigned nursing and ancillary personnel, utilizing both professional and supervisory discretion and independent judgment. Understands and adheres to the California Nurse Practice Act, The American Nurses Association (ANA) Code of Ethics for Nurses, the ANA Bill of Rights for Registered Nurses and the ANA Scope and Standards of Practice for Nursing. The Registered Nurse shall be responsible for the observation and direction of patient lifts and mobilization and shall participate as needed in patient handling. Speak and read English at a level that is sufficient to satisfactorily perform the essential functions of the position. Knowledge of standard office equipment (i.e., calculator, fax, photocopier) and personal computer and computer software skills (i.e., MS Windows, Excel, Access, Word, Powerpoint, internet, e-mail). Windows computer skills including proficient use of keyboarding, use of mouse or keys for functions such as selecting items, use of drop down menus, scroll bars, opening folders, copying and similar operations required upon employment or within the 1st two weeks of employment to perform the essential functions of the job. Performs other duties as assigned. Follows Palomar Health rules, policies, procedures, applicable laws and standards. Carries out the mission, vision, and quality commitment of Palomar Health.<p></p><h3 class="jobSectionHeader"><b><br>
Job Requirements</b></h3></div><p></p><div><div><div><b><br>
Minimum Education: </b></div><div>As required by certification and/or licensure</div></div><br>
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Preferred Education: </b></div><div>Bachelor's Degree</div></div><br>
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Minimum Experience: </b></div><div>1 year of directly related RN experience in area of specialty</div></div><br>
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Preferred Experience: </b></div><div>2+ years of directly related RN experience in area of specialty</div></div><br>
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Required Certification: </b></div><div>American Heart Association recognized BLS - Healthcare Provider</div></div><br>
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Preferred Certification: </b></div><div>Oncology Certified Nurse</div></div><br>
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Required License: </b></div><div>Current CA RN License</div></div><br>
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Preferred License: </b></div><div>Not Applicable</div></div></div></div>

Clinical RN II Medical Oncology $30K Hiring Incentive

Clinical RN II Medical Oncology $30K Hiring In

Virginia Oncology Associates

<div>Overview:
<div></div><div><b>
Virginia Oncology Associates, the largest group of medical professionals in Hampton Roads and Northeast North Carolina devoted exclusively to cancer care and blood disorders, has an exciting opportunity for a Clinical Research RN to support our office in Norfolk.</b></div><div></div><div><b><i><br>
***Please take this quick survey once you've submitted your resume to complete the application process: </i></b><b><i>Clinical Research PI Link</i></b></div><div></div><div><i><br>
****If you have completed the survey before, even for another position, please</i><b><i> do not take it again.</i></b></div>
Responsibilities:
<ul><li>Present trial concepts, objectives and treatment details to potential patients for various cellular therapy trials, while conducting detailed assessment and screening to determine their eligibility.</li><li>
Participating in the informed consent process and enrolling patients on protocol</li><li>
80% of the job will be computer based, and direct patient<i> care</i> is limited in a non-RN Clinical Research Coordinator role</li><li>
Collects and maintains regulatory documents in accordance with USOR SOP and applicable regulations. Participates in scheduling monitoring and auditing visits, as well as interacting with the monitors/auditors while onsite.</li><li>
Coordinating patient care in compliance with protocol requirements</li><li>
Collaborating with the physician to review patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to drug study and thoroughly documenting all findings</li><li>
Working directly with other research bases and/or sponsors</li><li>
Overseeing the preparation of orders by physicians to assure that protocol compliance is maintained</li><li>
Communicating with physicians regarding study requirements, need for dose modification and adverse event reporting</li></ul>
Qualifications:
<ul><li>Experience in clinical research preferred</li><li>
Experience with computer data entry and database management</li><li>
Excellent written and oral communication skills</li><li>
Ability to read, analyze, and interpret technical procedures such as protocols, informed consent, and regulatory documents</li><li>
Graduate from an accredited program for nursing education (BSN preferred)</li><li>
Minimum of one (1) year nursing experience, preferably in oncology</li><li>
Current licensure as an RN in Virginia preferred</li><li>
Current BCLS or ACLS certification required</li><li>
OCN, SoCRA, or ACRP certification preferred</li></ul><div></div><div><i><br>
WORK ENVIRONMENT:</i><br>
<i>The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment. While performing the duties of this job, the employee is regularly exposed to direct contact with patients with potential for exposure to toxic substances, medicinal preparations, and chemotherapeutic agents.</i></div><div></div><div><i><br>
PHYSICAL DEMANDS:</i><br>
<i>The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.</i></div></div><div></div>

Breast Cancer Clinical Research Nurse

OneOncology

<div><h1 class="jobSectionHeader"><b>Advanced Practice Provider Opportunity</b></h1>
<h3 class="jobSectionHeader"><b>Tennessee Oncology</b></h3>
<h5 class="jobSectionHeader"><b>Chattanooga, TN</b></h5><br>
<p></p>
<p><b>
Job Summary</b></p>
<p><b>
Occupation: </b>Nurse Practitioner or Physician Assistant</p>
<p><b>
Specialty:</b> Hematology/Oncology</p>
<p><b>
Clinic Location: </b>Tennessee Oncology</p>
<p><b>
Employment: </b>Full-Time | Mon-Fri | Hospitalist</p>
<p><b>
Setting</b><b>: </b>Private Practice, Inpatient</p>
<p><b>
Board Certifications: </b>NP-C/PA-C</p>
<p><b>
Ideal Candidate:</b></p>
<ul>
<li><p>Minimum of 1-2 years of APP experience required</p>
</li>
<li><p>Hematology/Oncology experience as RN or APP required</p>
</li>
<li><p>Hospitalist experience as RN or APP required</p>
</li>
</ul><p><b>Job Details:</b></p>
<ul>
<li><p>APP to support with inpatient rounding</p></li></ul><br>
<p>
</p><p><b>About the Role</b></p>
<p><b>
Tennessee Oncology</b> is seeking an Advanced Practice Provider to support its inpatient hematology and oncology services within a private practice hospital setting. In this role, you will provide inpatient rounding care, working primarily with hospitalized hematology patients while collaborating closely with physicians and the care team. The position offers significant clinical responsibility; APPs must be comfortable working autonomously in a hospital-based environment. This opportunity is well suited for an experienced APP with direct hospitalist and hematology/oncology experience who values independent practice, clinical depth, and patient-centered care.</p><br>
<p></p>
<p><b>
About Chattanooga, TN</b></p>
<p>
Chattanooga, Tennessee, offers an exceptional quality of life in a city celebrated for its natural beauty and vibrant community. Known as the &quot;Scenic City,&quot; Chattanooga is nestled along the Tennessee River and surrounded by the Appalachian Mountains, providing endless opportunities for outdoor recreation including hiking, cycling, and kayaking. The city boasts a revitalized downtown, thriving arts and culinary scenes, and nationally recognized attractions such as the Tennessee Aquarium and Lookout Mountain. With a growing economy, affordable cost of living, and ultra-fast municipal broadband, Chattanooga combines small-city charm with modern innovation, making it an ideal place to live and work.</p><br>
<p></p>
<p><b>
Recruitment Package</b></p>
<p><b>
Top-Tier Compensation</b> &ndash; Highly competitive compensation structures</p>
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Comprehensive Benefits</b> &ndash; Medical, Dental, Vision, Disability, Life</p>
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Retirement Plan</b> &ndash; Secure your future, 401k match</p>
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Work-Life Balance</b> &ndash; Paid time off</p>
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Professional Growth</b> &ndash; CME days and reimbursement</p>
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Community Care</b> &ndash; Make a real difference by caring for patients in their local communities</p><br>
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<p><b>
About the Practice</b></p>
<p><b>
Tennessee Oncology</b> is a leader in cancer care, built on a foundation of clinical excellence, compassionate care, and unwavering support for patients during some of the most challenging times in their lives. Our team of highly trained physicians and dedicated healthcare professionals is committed to delivering high-quality, evidence-based cancer care close to home. We proudly offer a comprehensive range of specialties, including Hematology/Medical Oncology, Radiation Oncology, Gynecologic Oncology, Breast Surgery, Palliative Care, and a robust Clinical Trials &amp; Research Program. At its heart, our mission is deeply committed to improving outcomes, advancing innovation, and supporting each patient with dignity and personalized care.</p>
<p>
Tennessee Oncology is proud to partner with <b>OneOncology</b>, a nationwide platform uniting premier independent specialty practices, including United Urology Group and SunState Medical Specialties. Together, we are advancing an integrated ecosystem of Medical Oncology, Urology, and Radiation Oncology, ensuring patients receive seamless, high-quality care across all aspects of their treatment journey. OneOncology's physician-led, data-driven, and technology-enabled model fosters collaboration, clinical excellence, and innovation across our network. Through shared platforms and programs like OneR, our non-exclusive clinical trial site management subsidiary, partner practices gain access to cutting-edge research and multi-center trials, allowing patients to benefit from the latest therapies and coordinated care, all within a single, patient-focused organization.</p><br>
<p></p>
<p>
If you would like to apply or learn more about this opportunity,<b> please email</b><b> your CV</b> to <b>shanna.carpien@oneoncology.com</b></p>
<p>
I look forward to speaking with you!</p></div>

Advanced Practice Provider - Tennessee Oncology

The START Center for Cancer Research

<div><p>The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval.</p><p>
The START Center for Cancer Research is seeking a <b>Clinical Research Coordinator, RN</b> who will work under the guidance of senior research staff to support the daily activities of early phase oncology clinical trials. The CRC, RN ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. This role involves direct patient interaction, data collection, and maintaining compliance with Good Clinical Practice (GCP). The Clinical Research Coordinator will be assigned multiple protocols at any time for which they will oversee the aspects of assigned protocols with planning and coordinating patient participation in the trial. Also, this role is responsible for implementation as well as completion of protocol specific requirements, providing accurate, up to date information to all team members involved with any aspect of carrying out protocol specific requirements.</p><p><b>
Work Schedule:</b><b> </b>Monday-Friday 8:00am-4:00pm</p><p><b>
Location:</b><b> </b>START Mountain Region</p><p></p><p><b><br>
Essential Responsibilities</b></p><ul><li>
Communicate on a regular basis with Study Sponsor&rsquo;s, CRO&rsquo;s, staff, etc. regarding questions, concerns, as well as status of the protocol.
</li><li>Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study.
</li><li>Create/review forms created or revised for assigned trials to assure protocol compliance.
</li><li>Maintain files using standardized study document labeling and filing procedures.
</li><li>Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.
</li><li>Maintain an up-to-date contact list.
</li><li>Assist with patient screening and determination of eligibility.
</li><li>Facilitate the informed consent process ensuring that consent is appropriately completed.
</li><li>Prepare and manage source documents according to standard operating procedures.
</li><li>Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations.
</li><li>Assist data coordinator team with case report form completion and query resolution.
</li><li>Work with the Principal Investigator to complete and submit Serious Adverse Event reports.
</li><li>Perform protocol specific closeout related activities in conjunction with the data coordinator.
</li><li>Provide documentation for all deviations whether related to the protocol or a SOP.
</li><li>Ensure that all team members involved understand and adhere to assigned protocols.
</li><li>Perform telephone triage assessments of patients on trial when necessary.</li><li>
Provide patient education regarding participation in a clinical trial, chemotherapy/biotherapy/investigational agent administration and potential side effects.</li></ul><p><b>
Required Education and Experience:</b></p><ul><li>
Associate&rsquo;s degree in Nursing.</li><li>
RN license in state practicing.</li><li>
2 years of clinical research experience.</li><li>
Basic understanding of oncology clinical trials, particularly Phase 1 studies.</li><li>
Strong attention to detail and accuracy in data collection and documentation.</li><li>
Ability to manage multiple tasks and meet deadlines in a fast-paced environment.</li><li>
Excellent organizational and time-management skills.</li><li>
Strong communication skills, both written and verbal.</li><li>
Ability to interact professionally with patients, study staff, and external stakeholders.</li><li>
Working knowledge of GCP and regulatory requirements.</li><li>
Proficient in Microsoft Office Suite and clinical trial management software.</li></ul><p><b>
Preferred Education and Experience:</b></p><ul><li>
Bachelor&rsquo;s degree in Nursing.
</li><li>Experience working in an oncology setting.</li></ul><p><b>
Physical &amp; Travel Requirements:</b></p><ul><li>
Approximately 80% of time is spent sitting.</li><li>
Very fast-paced and ever-changing healthcare environment.</li><li>
Demanding deadlines and time frames.</li><li>
Constant demand for updating knowledge.</li><li>
Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients.</li></ul><p><b>
Best-in-Class Benefits and Perks</b></p><p>
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:</p><ul><li>
Comprehensive health coverage: Medical, dental, and vision insurance provided</li><li>
Robust retirement planning: 401(k) plan available with employer matching</li><li>
Financial security: Life and disability insurance for added protection</li><li>
Flexible financial options: Health savings and flexible spending accounts offered</li><li>
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided</li><li>
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.</li></ul><p><b>
More about The START Center for Cancer Research</b></p><p>
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world&rsquo;s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.</p><p><b>
Ready to be part of a team changing the future of cancer treatment?</b></p><p>
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.</p><p>
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.</p></div><p></p>

Clinical Research Coordinator, RN

Texas Oncology

<div>Overview:<p></p><div><b><br>
Texas Oncology</b> is looking for a <b>Clinic Registered Nurse (RN)</b><b> </b>to join our team!<b> </b>This position will support our <b>Dallas Sammons</b> location<b>.</b> This is a full-time Monday-Friday hours (8:30am-5pm) position with no weekends, call or major holidays.</div><div><b><br>
</b></div><div><b>Texas Oncology </b>is the largest community oncology provider in the country and has approximately 600+ providers in 220+ sites across Texas and southeastern Oklahoma. Our founders pioneered community-based cancer care because they believed in making the best available cancer care accessible to all communities, allowing people to fight cancer at home with the critical support of family and friends nearby. Our mission is still the same today&mdash;at Texas Oncology, we use leading-edge technology and research to deliver high-quality, high-touch, evidence-based cancer care to help our patients achieve &ldquo;More breakthroughs. More victories.&rdquo; &reg; in their fight against cancer. Today, <b>Texas Oncology</b> treats half of all Texans diagnosed with cancer on an annual basis.</div><div></div><div><b><br>
Why work for us?</b></div><div>
Come join our team that is responsible for helping lead Texas Oncology in treating more patient diagnosed with cancer than any other provider in Texas. We offer our employees a competitive benefits package that includes Medical, Dental, Vision, Life Insurance, Short-term and Long-term disability coverage, a generous PTO program, a 401k plan that comes with a company match, a Wellness program that rewards you practicing a healthy lifestyle, and lots of other great perks such as Tuition Reimbursement, an Employee Assistance program and discounts on some of your favorite retailers.</div><div></div><div><b><br>
Join a Team That Invests in Your Future</b></div><div>
At Texas Oncology, we recognize the long-term impact of our people and are committed to rewarding performance and potential. That&rsquo;s why select roles may be eligible to participate in our Long-Term Incentive Plan (LTIP): an incentive program designed to attract, retain, and reward top talent.</div><div></div><div><b><br>
What is the Long-Term Incentive Plan (LTIP)?</b></div><div>
Long-Term Incentive Plan (LTIP): is an incentive program that typically vests over a three-year period and is tied to both individual performance and the operational success of Texas Oncology. Awards are discretionary and based on your position, performance, and potential for future career growth at Texas Oncology. Awards are reviewed and approved during the annual compensation review. LTIP awards are subject to your continued employment through the award payment date, and are governed by the written terms and conditions of the LTIP document.</div><div></div><div><b><br>
What does the Clinic Registered Nurse (RN) do?</b></div><div>
Under general supervision, the Registered Nurse (RN) provides professional nursing care for patients adhering to national and company standards and guidelines for specialty regulations. Must recognize physical, psychological, and spiritual aspects of care and participates in company-wide quality initiatives. Supports and adheres to the US Oncology Compliance Program, to include the Code of Ethics and Business Standards.</div>
Responsibilities:
<div><b>
The essential duties and responsibilities:</b></div><ul><li>
Plan, implement, coordinate, evaluate and promote the continuity of care consistent with established standards and practices.
</li><li>Assesses health status by interviewing patient regarding current status and medical history.</li><li>
Assesses patient/family needs and provides teaching and other instructional material.
</li><li>Provides psychosocial support to patients and families.</li><li>
Facilitates clinical operations and patient care</li><li>
Manages patient medication refill requests from the pharmacy telephone line and records the information in the patient chart.</li><li>
Facilitates and schedules consultations, pre-testing, diagnostic tests or procedures, referrals and future appointments for patients.</li><li>
Triages patient phone calls as needed and documents relevant information in the patient's chart.</li><li>
As necessary, facilitates communication between patient/family and interdisciplinary team and coordinates services related to patient care.</li><li>
Assist patients in locating available community resources.</li><li>
Inter professional collaboration</li><li>
Acts as a resource to LPN/LVNs and medical assistants.</li></ul>
Qualifications:
<div><b>
The ideal candidate for the Clinic Registered Nurse (RN) will have the following background and experience:<br>
</b></div><div></div><div><b>Education/Training</b></div><div><b>
Level I</b></div><ul><li>
Graduate from an accredited program for professional nursing education, BSN preferred.</li><li>
RN state license and current registration with the State Board of Nursing in practicing state.
</li><li>Current Basic Life Support (BLS) certification.
</li><li>Must maintain continuing education requirements.
</li><li>Entry level - 0-3 years nursing experience, oncology experience strongly preferred</li></ul><div><b>
Level II</b></div><ul><li>
Minimum three (3) years of nursing experience, oncology experience strongly preferred</li></ul><div><b>
Level Senior</b></div><ul><li><div><ul><li><div><ul><li>
In addition to levels I and II:<ul><li>
Minimum five (5) years nursing experience, including at least one year in oncology strongly preferred</li><li>
Oncology certification preferred</li></ul></li></ul></div></li></ul></div></li></ul><div></div><div><b><br>
Working Conditions:</b></div><div>
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. There is a possible exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment.</div><div></div><div><b><br>
Physical Requirements:</b></div><div>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.</div></div>

Clinical Staff RN Sr.- Dallas Sammons

Columbia University

<div><ul><li>Job Type: Officer of Administration</li>
<li>Regular/Temporary: Regular</li>
<li>Hours Per Week: 35+</li>
<li>Salary Range: $114,000 - $145,000</li>
</ul><div><i>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.</i></div>
<p></p>
<p>Position Summary</p>
<p>
Columbia University Irving Medical Center is seeking a Clinical Coordinator III (RN) to join the Bone Marrow Transplant team within the Division of Hematology/Oncology. This role delivers comprehensive patient care and education while supporting clinical operations and patient management, reporting directly to the Outpatient Oncology Nursing Directors.</p>
<p></p>
<p>Responsibilities</p>
<ul>
<li>Support the outpatient management of BMT/Cell Therapy patients in collaboration with MD/NP/PA providers</li>
<li>Assist with bone marrow procedures, including sterile setup, specimen collection, documentation, and patient monitoring</li>
<li>Coordinate all phases of the patient journey&mdash;from consultation through treatment and recovery</li>
<li>Perform comprehensive nursing assessments in person, by phone, and via the EMR</li>
<li>Oversee daily patient needs in clinic/infusion, including labs, test results, symptoms, and treatment planning</li>
<li>Partner with infusion and inpatient teams to ensure seamless care and accurate scheduling</li>
<li>Develop and deliver patient education related to oncology care and treatments</li>
<li>Address psychosocial needs of patients and caregivers</li>
<li>Provide compassionate, evidence‑based nursing care</li>
<li>Communicate patient needs to MD/NP/PA in a timely, clinically appropriate manner</li>
<li>Complete prior authorizations as needed</li>
<li>Prepare and review treatment calendars with patients</li>
<li>Incorporate cultural sensitivity and diversity into all aspects of care</li>
<li>Actively participate in a multidisciplinary team to support continuity of care</li>
<li>Perform additional duties as assigned</li>
</ul>
<p></p><p>Minimum Qualifications</p>
<ul>
<li>Bachelor&rsquo;s degree or equivalent education and experience, plus four years of related clinical experience.</li>
<li>Current New York State RN license and BLS certification.</li>
<li>Strong communication, interpersonal, and organizational skills.</li>
<li>Ability to adapt to a dynamic and fast-paced clinical environment.</li>
</ul>
<p></p><p>Preferred Qualifications</p>
<ul>
<li>Experience in medical oncology or bone marrow transplant (BMT).</li>
</ul>
<p></p><p>Other Requirements</p>
<ul>
<li>Medical clearance and participation in the medical surveillance program:
<ul><li>Direct patient contact and/or interaction with human research subjects.</li>
<li>Use of N-95 respirator as needed.</li>
<li>Potential exposure to bloodborne pathogens.</li>
</ul></li><li>Successful completion of all required compliance and systems training.</li>
</ul>
<p></p><p>Equal Opportunity Employer / Disability / Veteran</p>
<p>
Columbia University is committed to the hiring of qualified local residents.</p></div>

Clinical Coordinator III (RN) - Hematology & Oncology (BMT)

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