cancer registry coordinator

Dana-Farber Cancer Institute

<div><div><div><div>Job Ref:</div><div>
JR-2532</div></div> 
<div><div>Location:</div><div>
450 Brookline Ave, BOSTON, MA 02215</div> 
</div>
<div><div>Category:</div><div>
Clinical Research</div></div> 
<div><div>Employment Type:</div><div>
Full time</div></div> 
<div><div>Work Location:</div><div>
Onsite: 100% onsite</div></div> 
<div></div><div><div>Salary/Pay Rate:</div><div>
$48,100.00 - $54,400.00 per year</div>
</div></div>Overview
<div><div>The Center for Detection and Interception Blood Cancers is hiring a Clinical Research Coordinator to support non-interventional studies such as biobanking and observational studies. The CRC (Clinical Research Coordinators) work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required. Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements. May be responsible for pertinent IRB protocol submissions. This individual may also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the clinical trials management system, ONCORE. Some travel may be required. 
 
This position is considering 2026 bachelor&rsquo;s degree graduates.
Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals. 
<ul><li>
Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities</li><li>
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</li><li>
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</li><li>
Ensure all study related samples are collected, properly prepared, and shipped according to the protocol requirements and IATA/DOT regulations</li><li>
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</li><li>
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits</li><li>
Coordination and management of clinical trials throughout the trial life cycle, including communication with sponsors and regulatory authorities</li><li>
Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved</li><li>
Interact with study participants as directed/required by the protocol and/or study team</li><li>
May be responsible for tissue sample collection per trial requirements</li></ul>
KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:<ul><li>
Excellent organization and communications skills required</li><li>
Strong interpersonal skills &ndash; ability to effectively interact with all levels of staff and externals contacts</li><li>
Must be detail oriented</li><li>
Ability to effectively manage time and prioritize workload</li><li>
Must practice discretion and always adhere to hospital confidentiality guidelines</li><li>
Must have computer skills including the use of Microsoft Office</li></ul> 
MINIMUM JOB QUALIFICATIONS:
Bachelor&rsquo;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. 
SUPERVISORY RESPONSIBILITIES:
None
PATIENT CONTACT:
May have contact with Adult and Pediatric patients of all ages and populations. May distribute protocol schedules, quality of life surveys or other study-related questionnaires, subject diaries, and/or conduct follow-up communication with patients.
At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to .
Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.
<h3 class="jobSectionHeader">EEO Poster</h3>
.
Pay Transparency Statement
The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate&rsquo;s relevant experience, skills and qualifications.
For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA).
$48,100.00 - $54,400.00</div></div></div>

Clinical Research Coordinator - Center for Early Detection and Interception Blood Cancers

University of Virginia

<div>Looking to make a meaningful impact every day? The Office of Clinical Research (OCR) at the University of Virginia Comprehensive Cancer Center is looking for Clinical Research Coordinators, Non-Licensed (multiple levels) to support the advancement of innovative cancer research.
In this role, you will help bring new therapies from research to reality by coordinating oncology clinical trials and working closely with patients, physicians, and multidisciplinary research teams. You&rsquo;ll play a key part in ensuring studies are conducted efficiently, ethically, and in full compliance with regulatory and institutional standards.
This is an excellent opportunity for detail-oriented, collaborative professionals who are passionate about high-quality research and motivated to contribute to work that improves and extends patients&rsquo; lives.
What You&rsquo;ll Do<ul><li>
Recruit, screen, consent, and enroll participants across multiple cancer clinical trials</li><li>
Build trusted relationships with study participants through phone and in-person interactions</li><li>
Coordinate study visits and collect high-quality data at each visit</li><li>
Maintain accurate documentation, logs, and study materials</li><li>
Process, prepare, and ship laboratory specimens</li><li>
Track adverse events and ensure protocol compliance</li><li>
Collaborate closely with investigators and the research team to keep studies on track</li></ul>
What You&rsquo;ll Bring<ul><li>
Strong organizational skills and attention to detail</li><li>
A problem-solver mindset and comfort juggling multiple priorities</li><li>
Clear, compassionate communication (written and verbal)</li><li>
The ability to learn quickly and adapt in a fast-paced research environment</li><li>
A collaborative, team-first approach to your work</li></ul>
Why You&rsquo;ll Love This Role<ul><li>
Make a real impact in cancer research and patient care</li><li>
Join a mission-driven team at a top academic medical center</li><li>
Grow your clinical research career with support and mentorship</li><li>
Work in a role that blends science, organization, and meaningful human connection</li></ul>
Minimum Requirements for Roles under this Posting:
Clinical Research Coordinator 1, Non-Licensed ($27.80-29.30) 
Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications. 
Experience: None. Some experience in a healthcare setting and/or knowledge of medical terminology is preferred.
Clinical Research Coordinator- 2, Non-Licensed ($63,000 - $66,000) 
Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications. 
Experience: At least one year of clinical research experience. Some experience in a healthcare setting and/or knowledge of medical terminology is preferred.
Clinical Research Coordinator- 3, Non-Licensed ($71,500 - $74,500)
Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications. 
Experience: Minimum of 3 years of clinical research experience required. Master&rsquo;s degree may substitute for 1 year of clinical research experience. 
**Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is preferred at the time of hire and is required within one year.**
Clinical Research Coordinator- 4, Non-Licensed ($78,500 - $81,500)
Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications. 
Experience: At least seven years of clinical research experience demonstrating progressive levels of responsibility and complexity of work. Master&rsquo;s or other advanced degree may substitute for one year of clinical research experience. 
**Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is required.**
Physical Demands: This is primarily a sedentary job involving extensive use of desktop computers. The job does occasionally require traveling some distance to attend meetings, and programs.
Funding Details: This is a restricted position, which is dependent on funding and is contingent upon funding availability.
Work Arrangement: This position is based in Charlottesville, VA, and must be performed fully on-site.
About UVA and the Community: To learn more about UVA and in the Charlottesville area, visit UVA Life and Embark CVA.
This evergreen job posting is used to build a talent pool for the Clinical Research Coordinator Varying Levels (Non-Licensed) job family. Positions may open periodically within the [Cancer Center], and applications to this pool will be reviewed on a recurring basis.
Key Information<ul><li>
This is not a posting for a single, immediate vacancy.</li><li>
Applicants may be considered for any CRC role for which they meet the minimum qualifications.</li><li>
Applications remain active for a limited time and are reviewed and dispositioned quarterly.</li><li>
If you need to update your application, please visit your Applicant Profile and edit any relevant saved information, or contact the supporting recruiter listed for this requisition.</li><li>
Candidates who are still interested after a review cycle closes are encouraged to reapply to future evergreen postings.</li></ul>
Submitting an application indicates your interest in future Clinical Research Coordinator opportunities within the UVA School of Medicine Cancer Center.
Background Check: Background checks, pre-employment health screenings, and drug screenings will be conducted on all new hires prior to employment.
Visa Sponsorship: This position will not consider candidates who require immigration sponsorship now or in the future.
How to Apply: Please apply online, by searching for requisition number R0081545. Complete an application with the following documents:
<ul><li>Resume
</li><li>Cover Letter</li></ul>
Upload all materials into the resume submission field. You can submit multiple documents into this one field or combine them into one PDF. Applications without all required documents will not receive full consideration.
Internal applicants: Search and apply for jobs on the UVA Internal Careers website.
Reference Check Process: Reference checks will be completed by UVA&rsquo;s third-party partner, SkillSurvey, during the final phase of the interview. Five references will be requested, with at least three responses required.
Recruiter Contact: For questions about the application process, please contact Jeremy Brofft.
MINIMUM REQUIREMENTS
Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications.
Experience: None. Some experience in a healthcare setting and/or knowledge of medical terminology is preferred.
Licensure: None.
PHYSICAL DEMANDS
This is primarily a sedentary job involving extensive use of desktop computers. The job does occasionally require traveling some distance to attend meetings, and programs.
The University of Virginia is an equal opportunity employer. All interested persons are encouraged to apply, including veterans and individuals with disabilities. Learn more about UVA&rsquo;s commitment to non-discrimination and equal opportunity employment.</div>

Clinical Research Coordinator-Varying Levels(Non-Licensed)-Cancer Center

Mount Sinai Health System

<div>
 
 Description
 
 
 
 A Clinical Research Coordinator (CRC) I position is currently available within the Tisch Cancer Center. Duties will include activities such as, but no limited to, data collection, specimen collection, obtaining informed consent, and maintaining and organizing study information.
 
 
 The Tisch Cancer Center is a vital component of the Icahn School of Medicine at Mount Sinai Hospital and plays a key role in the Mount Sinai Health System, which is one of the largest health care systems in the nation. We are a National Cancer Institute (NCI)-designated center and provide a multidisciplinary approach to cancer treatments and clinical breakthroughs that may one day put an end to cancer.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Collects and records study data; inputs all information into database.
 </li>
 <li>
 Under direct supervision of the Principle Investigator(s), obtains informed consent and educates participants regarding study requirements.
 </li>
 <li>
 Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, and administering lifestyle questionnaires.
 </li>
 <li>
 Maintains source documents and subject files in accordance with hospital procedures; helps to ensure accurate and complete compilation of subject data through chart reviews.
 </li>
 <li>
 Secures, delivers and ships clinical specimens as required by the protocol.
 </li>
 <li>
 Responsible for organizing and preparing for monitoring visits.
 </li>
 <li>
 Assists with coordination and management of clinical trials including communication with Sponsors.
 </li>
 <li>
 Performs other related duties as assigned.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelors or Masters degree in Science or closely related field.
 </li>
 <li>
 No experience required; One year of research experience preferred.
 
 
 </li>
 </ul>
 
 Employer Description
 
 
 
 
 Strength through Unity and Inclusion
 
 
 
 The Mount Sinai Health System is committed to fostering an environment where everyone can contribute to excellence. We share a common dedication to delivering outstanding patient care. When you join us, you become part of Mount Sinai&rsquo;s unparalleled legacy of achievement, education, and innovation as we work together to transform healthcare. We encourage all team members to actively participate in creating a culture that ensures fair access to opportunities, promotes inclusive practices, and supports the success of every individual.
 
 
 At Mount Sinai, our leaders are committed to fostering a workplace where all employees feel valued, respected, and empowered to grow. We strive to create an environment where collaboration, fairness, and continuous learning drive positive change, improving the well-being of our staff, patients, and organization. Our leaders are expected to challenge outdated practices, promote a culture of respect, and work toward meaningful improvements that enhance patient care and workplace experiences. We are dedicated to building a supportive and welcoming environment where everyone has the opportunity to thrive and advance professionally. Explore this opportunity and be part of the next chapter in our history.
 
 
 
 About The Mount Sinai Health System
 
 
 
 Mount Sinai Health System is one of the largest academic medical systems in the New York metro area, with more than 48,000 employees working across eight hospitals, more than 400 outpatient practices, more than 300 labs, a school of nursing, and a leading school of medicine and graduate education. Mount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time &mdash; discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it. Through the integration of its hospitals, labs, and schools, Mount Sinai offers comprehensive health care solutions from birth through geriatrics, leveraging innovative approaches such as artificial intelligence and informatics while keeping patients&rsquo; medical and emotional needs at the center of all treatment. The Health System includes more than 9,000 primary and specialty care physicians; 13 joint-venture outpatient surgery centers throughout the five boroughs of New York City, Westchester, Long Island, and Florida; and more than 30 affiliated community health centers. We are consistently ranked by U.S. News &amp; World Report's Best Hospitals, receiving high "Honor Roll" status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology. New York Eye and Ear Infirmary of Mount Sinai is ranked No. 12 in Ophthalmology. U.S. News &amp; World Report&rsquo;s &ldquo;Best Children&rsquo;s Hospitals&rdquo; ranks Mount Sinai Kravis Children's Hospital among the country&rsquo;s best in several pediatric specialties. The Icahn School of Medicine at Mount Sinai is ranked No. 11 nationwide in National Institutes of Health funding and in the 99th percentile in research dollars per investigator according to the Association of American Medical Colleges. Newsweek&rsquo;s &ldquo;The World&rsquo;s Best Smart Hospitals&rdquo; ranks The Mount Sinai Hospital as No. 1 in New York and in the top five globally, and Mount Sinai Morningside in the top 20 globally.
 
 
 
 Equal Opportunity Employer
 
 
 
 The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law. We are deeply committed to fostering an environment where all faculty, staff, students, trainees, patients, visitors, and the communities we serve feel respected and supported. Our goal is to create a healthcare and learning institution that actively works to remove barriers, address challenges, and promote fairness in all aspects of our organization.
 
 
 
 Compensation
 
 
 
 The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $58661 - $73530 Annually. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.
</div>

Clinical Research Coordinator I - Tisch Cancer Center

Trinity Health

<div>
 
 Employment Type:
 
 
 
 Full time
 
 
 
 Shift:
 
 
 
 Day Shift
 
 
 
 Description:
 
 
 
 Oncology Research Coordinator
 
 
 
 Department:
 
 Oncology Research
 
 
 
 Location:
 
 Trinity Health Ann Arbor
 
 
 
 Minimum rate of pay: $26.97 PLUS DailyPAY
 
 
 
 
 Total Rewards and Benefits:
 
 
 
 <ul>
 <li>
 Competitive compensation, DAILYPAY
 </li>
 <li>
 Benefits effective Day One! No waiting periods.
 </li>
 <li>
 Full benefits package including Medical, Dental, Vision, PTO, Life Insurance, Short and Long-Term Disability
 </li>
 <li>
 Retirement savings plan with employer match and contributions
 </li>
 <li>
 Opportunity for growth and advancement throughout Trinity Health
 </li>
 <li>
 Tuition Reimbursement
 
 
 
 </li>
 </ul>
 
 Position Purpose:
 
 
 
 Will work with federally funded Michigan Cancer Research Consortium NCI Community Oncology Research Program at Trinity Health Ann Arbor Hospital. Responsible for direct coordination of all eligibility confirmation, registration, data interpretation and reporting, laboratory specimens, and regulatory requirements necessary for oncology research trials associated with the Michigan Cancer Research Consortium (MCRC). Works with all study sponsors (federal and industry) to assure MCRC sites meet all standards associated with Human Subjects and Federal regulations appropriate to clinical trials. Provides support to health care providers, clinical research nurses, and ancillary departments to assure care is provided per protocol standards. Provides mentorship, training and professional guidance to investigators, other research coordinators, and nurses at sub- recipient sites of the Michigan Cancer Research Consortium (14 hospitals in 3 states).
 
 
 
 Shifts Available:
 
 Days
 
 
 
 Status Available:
 
 Full-time, 40 hours/week
 
 
 
 Required Qualifications:
 
 
 
 
 Education:
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree, preferably in science-based field.
 
 
 
 </li>
 </ul>
 
 Experience:
 
 
 
 <ul>
 <li>
 Two years of related data, health care, or previous research experience preferred.
 </li>
 <li>
 Knowledge of research design principles, statistics, regulatory requirements, and ethical requirements.
 
 
 
 </li>
 </ul>
 
 Physical and Mental Requirements and Working Conditions:
 
 
 
 <ul>
 <li>
 Demonstrated ability to work closely with principal investigators and other stakeholders to coordinate the day-to-day activities required in study coordination.
 </li>
 <li>
 Excellent writing and interpersonal communication skills.
 </li>
 <li>
 Excellent organizational and troubleshooting skills.
 </li>
 <li>
 Ability to work both independently and in team-oriented settings.
 </li>
 <li>
 Ability to work flexible hours to accommodate study and patient schedules.
 </li>
 <li>
 Must be able to set and organize own work priorities and adapt to them as they change frequently.
 </li>
 <li>
 Must be able to work concurrently on a variety of tasks/projects in an environment that may be stressful with individuals having diverse personalities and work styles.
 </li>
 <li>
 Must be able to travel within the local community, across a continuum of care, to the various Trinity Health sites (10-50%) as needed.
 
 
 
 </li>
 </ul>
 
 What you will do:
 
 
 
 <ul>
 <li>
 Provides direct coordination of all patient registrations for a wide variety of clinical trials (100+) for all 14 MCRC hospitals. Reviews eligibility materials to ensure patient eligibility for each trial and that documentation meets acceptable standards per study sponsor and federal guidelines.
 </li>
 <li>
 Provides consultation with and feedback to oncologists (medical, radiation and surgical), nurses and other research coordinators related to eligibility requirements for patients in a wide variety of pharmaceutical and National Cancer Institute sponsored oncology clinical research protocols.
 </li>
 <li>
 Abstracts and reports data in multiple electronic data capture systems per study specific direction. Provides consultation to research nurses and ancillary departments on study required documentation and submission guidelines.
 </li>
 <li>
 Independently evaluates potential research study protocols for feasibility and resource capabilities. Coordinates with study sponsors to answer queries, provide information on MCRC SOP's and act as the liaison to clinical team.
 </li>
 <li>
 Evaluates medical records to abstract patient information on performance status, response to investigational treatment and severity of toxicities based on protocol requirements.
 </li>
 <li>
 Consults with national research bases and industry sponsors related to protocol clarifications on behalf of investigators and patients to assure protocol compliance and patient safety.
 </li>
 <li>
 Provides training, education, orientation and supervision to research coordinators and nurses at all 14 sites of the Michigan Cancer Research Consortium Clinical Community.
 </li>
 <li>
 Assures that research specimens are obtained and processed appropriately and works closely with pathology and interventional radiology departments regarding biopsies and tissue acquisition.
 </li>
 <li>
 Assures radiologic images are uploaded into the appropriate database, and radiation treatment plans for participants are submitted to each research base per study specific guidelines.
 </li>
 <li>
 Represents MCRC at National Meetings and Industry Sponsored events related to clinical trials.
 </li>
 <li>
 Analyzes and evaluates clinical data to assess for trends of potential adverse events. Recognizes and reports potential adverse events in cooperation with the research nurses, investigators, and principal investigator.
 </li>
 <li>
 Acts as patient advocate between the investigator, clinical departments, and the cooperative groups.
 </li>
 <li>
 Serves as liaison to other departments, outside organizations, and industry representatives on related research study or clinical trial issues.
 
 
 
 </li>
 </ul>
 Click Here to learn more about the benefits, culture, and career development opportunities available to you at Trinity Health Michigan.
 
 
 
 Our Commitment
 
 
 
 Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.
 
 
 
 00651273
 
</div>

Oncology Research Coordinator

Employment Type: 
Full time
 
Shift: 
Day Shift
 
Description: 
Oncology Research Coordinator
 
Department: Oncology Research
 
Location: Trinity Health Ann Arbor
 
Minimum rate of pay: $26.97 PLUS DailyPAY
 
Total Rewards and Benefits: 
<ul>
<li>Competitive compensation,DAILYPAY</li>
<li>Benefits effective Day One! No waiting periods.</li>
<li>Full benefits package including Medical, Dental, Vision, PTO, Life Insurance, Short and Long-Term Disability</li>
<li>Retirement savings plan with employer match and contributions</li>
<li>Opportunity for growth and advancement throughout Trinity Health</li>
<li>Tuition Reimbursement</li>
</ul>
Position Purpose: 
Will work with federally funded Michigan Cancer Research Consortium NCI Community Oncology Research Program at Trinity Health Ann Arbor Hospital. Responsible for direct coordination of all eligibility confirmation, registration, data interpretation and reporting, laboratory specimens, and regulatory requirements necessary for oncology research trials associated with the Michigan Cancer Research Consortium (MCRC). Works with all study sponsors (federal and industry) to assure MCRC sites meet all standards associated with Human Subjects and Federal regulations appropriate to clinical trials. Provides support to health care providers, clinical research nurses, and ancillary departments to assure care is provided per protocol standards. Provides mentorship, training and professional guidance to investigators, other research coordinators, and nurses at sub- recipient sites of the Michigan Cancer Research Consortium (14 hospitals in 3 states).
 
Shifts Available: Days
 
Status Available: Full-time, 40 hours/week
 
Required Qualifications: 
Education: 
<ul>
<li>Bachelor’s degree, preferably in science-based field.</li>
</ul>
Experience: 
<ul>
<li>Two years of related data, health care, or previous research experience preferred.</li>
<li>Knowledge of research design principles, statistics, regulatory requirements, and ethical requirements.</li>
</ul>
Physical and Mental Requirements and Working Conditions: 
<ul>
<li>Demonstrated ability to work closely with principal investigators and other stakeholders to coordinate the day-to-day activities required in study coordination.</li>
<li>Excellent writing and interpersonal communication skills.</li>
<li>Excellent organizational and troubleshooting skills.</li>
<li>Ability to work both independently and in team-oriented settings.</li>
<li>Ability to work flexible hours to accommodate study and patient schedules.</li>
<li>Must be able to set and organize own work priorities and adapt to them as they change frequently.</li>
<li>Must be able to work concurrently on a variety of tasks/projects in an environment that may be stressful with individuals having diverse personalities and work styles.</li>
<li>Must be able to travel within the local community, across a continuum of care, to the various Trinity Health sites (10-50%) as needed.</li>
</ul>
What you will do: 
<ul>
<li>Provides direct coordination of all patient registrations for a wide variety of clinical trials (100+) for all 14 MCRC hospitals. Reviews eligibility materials to ensure patient eligibility for each trial and that documentation meets acceptable standards per study sponsor and federal guidelines.</li>
<li>Provides consultation with and feedback to oncologists (medical, radiation and surgical), nurses and other research coordinators related to eligibility requirements for patients in a wide variety of pharmaceutical and National Cancer Institute sponsored oncology clinical research protocols.</li>
<li>Abstracts and reports data in multiple electronic data capture systems per study specific direction. Provides consultation to research nurses and ancillary departments on study required documentation and submission guidelines.</li>
<li>Independently evaluates potential research study protocols for feasibility and resource capabilities. Coordinates with study sponsors to answer queries, provide information on MCRC SOP's and act as the liaison to clinical team.</li>
<li>Evaluates medical records to abstract patient information on performance status, response to investigational treatment and severity of toxicities based on protocol requirements.</li>
<li>Consults with national research bases and industry sponsors related to protocol clarifications on behalf of investigators and patients to assure protocol compliance and patient safety.</li>
<li>Provides training, education, orientation and supervision to research coordinators and nurses at all 14 sites of the Michigan Cancer Research Consortium Clinical Community.</li>
<li>Assures that research specimens are obtained and processed appropriately and works closely with pathology and interventional radiology departments regarding biopsies and tissue acquisition.</li>
<li>Assures radiologic images are uploaded into the appropriate database, and radiation treatment plans for participants are submitted to each research base per study specific guidelines.</li>
<li>Represents MCRC at National Meetings and Industry Sponsored events related to clinical trials.</li>
<li>Analyzes and evaluates clinical data to assess for trends of potential adverse events. Recognizes and reports potential adverse events in cooperation with the research nurses, investigators, and principal investigator.</li>
<li>Acts as patient advocate between the investigator, clinical departments, and the cooperative groups.</li>
<li>Serves as liaison to other departments, outside organizations, and industry representatives on related research study or clinical trial issues.</li>
</ul>
Click Here to learn more about the benefits, culture, and career development opportunities available to you at Trinity Health Michigan.
 
Our Commitment
 
Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.

<div>Description
A Clinical Research Coordinator (CRC) I position is currently available within the Tisch Cancer Center. Duties will include activities such as, but no limited to, data collection, specimen collection, obtaining informed consent, and maintaining and organizing study information. 
The Tisch Cancer Center is a vital component of the Icahn School of Medicine at Mount Sinai Hospital and plays a key role in the Mount Sinai Health System, which is one of the largest health care systems in the nation. We are a National Cancer Institute (NCI)-designated center and provide a multidisciplinary approach to cancer treatments and clinical breakthroughs that may one day put an end to cancer. 
Responsibilities<ul><li>
Collects and records study data; inputs all information into database.</li><li>
Under direct supervision of the Principle Investigator(s), obtains informed consent and educates participants regarding study requirements.</li><li>
Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, and administering lifestyle questionnaires.</li><li>
Maintains source documents and subject files in accordance with hospital procedures; helps to ensure accurate and complete compilation of subject data through chart reviews.</li><li>
Secures, delivers and ships clinical specimens as required by the protocol.</li><li>
Responsible for organizing and preparing for monitoring visits.</li><li>
Assists with coordination and management of clinical trials including communication with Sponsors.</li><li>
Performs other related duties as assigned.</li></ul> 

Qualifications<ul><li>
Bachelors or Masters degree in Science or closely related field.</li><li>
No experience required; One year of research experience preferred.</li></ul> 

Employer Description
Strength through Unity and Inclusion

The Mount Sinai Health System is committed to fostering an environment where everyone can contribute to excellence. We share a common dedication to delivering outstanding patient care. When you join us, you become part of Mount Sinai&rsquo;s unparalleled legacy of achievement, education, and innovation as we work together to transform healthcare. We encourage all team members to actively participate in creating a culture that ensures fair access to opportunities, promotes inclusive practices, and supports the success of every individual.

At Mount Sinai, our leaders are committed to fostering a workplace where all employees feel valued, respected, and empowered to grow. We strive to create an environment where collaboration, fairness, and continuous learning drive positive change, improving the well-being of our staff, patients, and organization. Our leaders are expected to challenge outdated practices, promote a culture of respect, and work toward meaningful improvements that enhance patient care and workplace experiences. We are dedicated to building a supportive and welcoming environment where everyone has the opportunity to thrive and advance professionally. Explore this opportunity and be part of the next chapter in our history.

About the Mount Sinai Health System:

Mount Sinai Health System is one of the largest academic medical systems in the New York metro area, with more than 48,000 employees working across eight hospitals, more than 400 outpatient practices, more than 300 labs, a school of nursing, and a leading school of medicine and graduate education. Mount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time &mdash; discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it. Through the integration of its hospitals, labs, and schools, Mount Sinai offers comprehensive health care solutions from birth through geriatrics, leveraging innovative approaches such as artificial intelligence and informatics while keeping patients&rsquo; medical and emotional needs at the center of all treatment. The Health System includes more than 9,000 primary and specialty care physicians; 13 joint-venture outpatient surgery centers throughout the five boroughs of New York City, Westchester, Long Island, and Florida; and more than 30 affiliated community health centers. We are consistently ranked by U.S. News &amp; World Report's Best Hospitals, receiving high &quot;Honor Roll&quot; status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology. New York Eye and Ear Infirmary of Mount Sinai is ranked No. 12 in Ophthalmology. U.S. News &amp; World Report&rsquo;s &ldquo;Best Children&rsquo;s Hospitals&rdquo; ranks Mount Sinai Kravis Children's Hospital among the country&rsquo;s best in several pediatric specialties. The Icahn School of Medicine at Mount Sinai is ranked No. 11 nationwide in National Institutes of Health funding and in the 99th percentile in research dollars per investigator according to the Association of American Medical Colleges. Newsweek&rsquo;s &ldquo;The World&rsquo;s Best Smart Hospitals&rdquo; ranks The Mount Sinai Hospital as No. 1 in New York and in the top five globally, and Mount Sinai Morningside in the top 20 globally.

Equal Opportunity Employer

The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law. We are deeply committed to fostering an environment where all faculty, staff, students, trainees, patients, visitors, and the communities we serve feel respected and supported. Our goal is to create a healthcare and learning institution that actively works to remove barriers, address challenges, and promote fairness in all aspects of our organization. 
Compensation
The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $58661 - $73530 Annually. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.</div>

<div>Looking to make a meaningful impact every day? The Office of Clinical Research (OCR) at the University of Virginia Comprehensive Cancer Center is looking for Clinical Research Coordinators, Licensed (multiple levels) to support the advancement of innovative cancer research.
In this role, you will combine your clinical nursing expertise with research coordination to help bring new cancer therapies from study to standard of care by coordinating oncology clinical trials and working closely with patients, physicians, and multidisciplinary research teams. You&rsquo;ll play a key part in ensuring studies are conducted efficiently, ethically, and in full compliance with regulatory and institutional standards.
This is an excellent opportunity for detail-oriented, collaborative professionals who are passionate about high-quality research and motivated to contribute to work that improves and extends patients&rsquo; lives.
What You&rsquo;ll Do<ul><li>
Recruit, screen, consent, and enroll participants across multiple cancer clinical trials</li><li>
Build trusted relationships with study participants through phone and in-person interactions</li><li>
Coordinate study visits and collect high-quality data at each visit</li><li>
Maintain accurate documentation, logs, and study materials</li><li>
Process, prepare, and ship laboratory specimens</li><li>
Track adverse events and ensure protocol compliance</li><li>
Collaborate closely with investigators and the research team to keep studies on track</li><li>
Integrate nursing skills into clinical research activities</li></ul>
What You&rsquo;ll Bring<ul><li>
Strong organizational skills and attention to detail</li><li>
A problem-solver mindset and comfort juggling multiple priorities</li><li>
Clear, compassionate communication (written and verbal)</li><li>
The ability to learn quickly and adapt in a fast-paced research environment</li><li>
A collaborative, team-first approach to your work</li></ul>
Why You&rsquo;ll Love This Role<ul><li>
Make a real impact in cancer research and patient care</li><li>
Join a mission-driven team at a top academic medical center</li><li>
Grow your clinical research career with support and mentorship</li><li>
Work in a role that blends science, organization, and meaningful human connection</li></ul>
Minimum Requirements for Roles under this Posting:
Clinical Research Coordinator 1, Licensed ($32.65 - $35.57/hr) 
Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications. Nursing Diploma may substitute for Degree for Licensed Registered Nurse. 
Licensure: Licensed to Practice in Clinical Profession such as (but not limited to): Registered Nurse, Athletic Training, Pharmacology, Medical Technology, Physical Therapy or Registered Respiratory Therapy.
Clinical Research Coordinator- 2, Licensed ($73,000 - $76,000) 
Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications. Nursing Diploma may substitute for Degree for Licensed Registered Nurse. 
Experience: At least one year of clinical research experience. 
Licensure: Licensed to Practice in Clinical Profession such as (but not limited to): Registered Nurse, Athletic Training, Pharmacology, Medical Technology, Physical Therapy or Registered Respiratory Therapy.
Clinical Research Coordinator- 3, Licensed ($81,500 - $84,500)
Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications. Nursing Diploma may substitute for Degree for Licensed Registered Nurse. 
Experience: A minimum of 3 years of clinical research experience required. Master&rsquo;s or advanced degree may substitute for 1 year of clinical research experience. 
Licensure: Licensed to Practice in Clinical Profession such as (but not limited to): Registered Nurse, Athletic Training, Pharmacology, Medical Technology, Physical Therapy or Registered Respiratory Therapy.
Clinical Research Coordinator- 4, Licensed ($88,500 - $91,500) 
Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications. Nursing Diploma may substitute for Degree for Licensed Registered Nurse.
 
Experience: At least seven years of clinical research experience demonstrating progressive levels of responsibility and complexity of work. Master&rsquo;s or other advanced degree may substitute for one year of clinical research experience.
Licensure: Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is required. Licensed to Practice in Clinical Profession such as (but not limited to): Registered Nurse, Athletic Training, Pharmacology, Medical Technology, Physical Therapy or Registered Respiratory Therapy.
Physical Demands: This is primarily a sedentary job involving extensive use of desktop computers. The job does occasionally require traveling some distance to attend meetings, and programs.
Funding Details: This is a restricted position, which is dependent on funding and is contingent upon funding availability.
Work Arrangement: This position is based in Charlottesville, VA, and must be performed fully on-site.
About UVA and the Community: To learn more about UVA and in the Charlottesville area, visit UVA Life and Embark CVA.
This evergreen job posting is used to build a talent pool for the Clinical Research Coordinator- Varying Levels (Licensed) job family. Positions may open periodically within the [Cancer Center], and applications to this pool will be reviewed on a recurring basis.
Key Information<ul><li>
This is not a posting for a single, immediate vacancy.</li><li>
Applicants may be considered for any CRC role for which they meet the minimum qualifications.</li><li>
Applications remain active for a limited time and are reviewed and dispositioned quarterly.</li><li>
If you need to update your application, please visit your Applicant Profile and edit any relevant saved information, or contact the supporting recruiter listed for this requisition.</li><li>
Candidates who are still interested after a review cycle closes are encouraged to reapply to future evergreen postings.</li></ul>
Submitting an application indicates your interest in future Clinical Research Coordinator opportunities within the UVA School of Medicine Cancer Center.
Background Check: Background checks, pre-employment health screenings, and drug screenings will be conducted on all new hires prior to employment.
Visa Sponsorship: This position will not consider candidates who require immigration sponsorship now or in the future.
How to Apply: Please apply online, by searching for requisition number R0081542. Complete an application with the following documents:
<ul><li>Resume
</li><li>Cover Letter</li></ul>
Upload all materials into the resume submission field. You can submit multiple documents into this one field or combine them into one PDF. Applications without all required documents will not receive full consideration.
Internal applicants: Search and apply for jobs on the UVA Internal Careers website.
Reference Check Process: Reference checks will be completed by UVA&rsquo;s third-party partner, SkillSurvey, during the final phase of the interview. Five references will be requested, with at least three responses required.
Contact: For questions about the application process, please contact Jeremy Brofft, Senior Academic Recruiter at xmf9ad@virginia.edu.
The University of Virginia is an equal opportunity employer. All interested persons are encouraged to apply, including veterans and individuals with disabilities. Learn more about UVA&rsquo;s commitment to non-discrimination and equal opportunity employment.</div>

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