Clinical Research Coordinator II - Hematology/Oncology
$60k - $75kUniversity of Chicago
- # Clinical Research Coordinator II - Hematology/OncologyApplyremote type: Onsitelocations: Chicago, ILtime type: Full timeposted on: Posted Yesterdayjob requisition id: JR34759**Department**BSD MED - Hematology and Oncology - Clinical Research Staff - Cluster 9**About the Department**The Section of Hematology/Oncology has a proud and long tradition of excellence in research-based patient care and clinical discovery. Ranked among the finest cancer programs in the country, the Section is comprised of nationally and internationally known faculty with expertise in all major types of malignancies, blood disorders, and experimental therapies.**Job Summary**The Clinical Research Coordinator II (CRC2) is a specialized researcher partnering with the clinical Principal Investigator (PI) and under the direction of a departmental or lab research manager. While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC2 supports, facilitates and coordinates independently the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties with limited supervision and/or guidance, the CRC2 works with the PI, department, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.**Responsibilities*** Manages all aspects of conducting clinical trials including screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.* Recruits and interviews potential study patients with guidance from PI and other clinical research staff.* Collects, processes, ships and stores specimens to appropriate laboratory according to established aseptic techniques.* Identifies and explains the responsibilities of principal investigators, research team members, sponsors, contract research organizations (CROs), and regulatory authorities related to the conduct of a clinical trial.* Coordinates the conduct of the study from startup through closeout including recruitment and screening of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence.* Plans and coordinates patient schedule for study procedures, return visits, and study treatment schedules.* Educates patients about study procedures to be performed, visit schedule, what to report between and during visits, and the risks and benefits of the procedures.* Performs assessments at visits and monitors for adverse events.* Organizes and attends site visits from sponsors and other relevant study meetings.* Protects patients' and data confidentiality by ensuring security of research data and personal health information and compliance with federal regulations and sponsor protocols.* Ensures standard operating procedures (SOP) are implemented and documented in accordance to study sponsor, primary investigator, and regulatory agency specifications.* Maintains accurate and complete records which may include, but are not limited to, signed informed consent, relevant IRB approvals, source documentation, case report forms (CRF's), drug dispensing logs, and study related communication.* Understands the IRB submission and review process, and when and how to apply for IRB review, including facilitation of study initiation through meticulous and timely preparation of IRB submissions independently.* Ensures compliance with federal regulations and institutional policies.* May prepare and maintain protocol submissions and revisions.* Assists in the training of new or backup coordinators.* Analyzes, facilitates and participates in the daily activities of multiple moderately complex clinical trials and performs all aspects of clinical data management, including patient data retrieval, referring MD office records, preparing clinical research charts, and participation in program audits.* Solves a range of straightforward problems relating to the administration of the compliance, financial and other related aspects of a clinical study.* Accountable for all tasks in moderately complex clinical studies.* Facilitates and participates in the daily activities of moderately complex clinical studies and performs various activities including patient data retrieval, documenting clinical research records, and participation in program audits.* Performs other related work as needed.**Minimum Qualifications****Education:**Minimum requirements include a college or university degree in related field.**Work Experience:**Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.**Certifications:****---****Preferred Qualifications****Education:*** Bachelors degree.**Experience:*** Clinical research experience or relevant experience.* Background coordinating multiple studies, including investigator initiated, industry sponsored, and multi-site trials.**Technical Skills or Knowledge:*** Comprehend technical documents.**Preferred Competencies*** Communicate in writing.* Communicate orally.* Condense complicated issues to simple summaries that can be understood by a variety of constituents.* Create and deliver presentations.* Develop and manage interpersonal relationships.* Exercise absolute discretion regarding confidential matters.* Follow written and/or verbal instructions.* Give directions.* Handle sensitive matters with tact and discretion.* Handle stressful situations.* Learn and develop skills.* Maintain a high level of alertness.* Pay attention to detail.* Perform multiple tasks simultaneously.* Prioritize work and meet deadlines.* React effectively, quickly, calmly, and rationally during conflicts and emergencies.* Train or teach others.* Work effectively and collegially with little supervision or as member of a team.* Work independently.**Working Conditions*** Aware of safety hazards and take appropriate precautions.**Application Documents*** Resume/CV (required)* Cover Letter (required)The University of Chicago uses AI-assisted tools to streamline and augment some recruitment processes; however, AI is not used to make hiring decisions. When applying, the document(s) **MUST** be uploaded via the **My Experience** page, in the section titled **Application Documents** of the application.**Job Family**Research**Role Impact**Individual Contributor**Scheduled** **Weekly Hours**37.5**Drug Test Required**Yes**Health Screen Required**Yes**Motor Vehicle Record Inquiry Required**No**Pay Rate Type**Salary **FLSA Status**Exempt **Pay Range**$60,000.00 - $75,000.00The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting.**Benefits Eligible**YesThe University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook.**Posting Statement**The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, shared ancestry, age, status as an individual with a disability, military or veteran status, genetic information, or other protected classes under the law. For additional information please see the University's Notice of Nondiscrimination. Job seekers in need of a reasonable accommodation to complete the application process should call View phone number on click.appcast.io or submit a request via Applicant Inquiry Form. All offers of employment are contingent upon a background check that includes a review of conviction history. A conviction does not automatically preclude University employment. Rather, the University considers conviction information on a case-by-case basis and assesses the nature of the offense, the circumstances surrounding it, the proximity in time of the conviction, and its relevance to the position. The University of Chicago's Annual Security & Fire Safety Report (Report) provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information. The Report can be accessed online at: Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637.
- J-18808-Ljbffr The University Of Chicago
Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the Clinical Research Coordinator II - Hematology/Oncology in Chicago, IL vacancy
$31 per hour
...Position Details Position Details Job Title CLINICAL RESEARCH COORDINATOR II Position Number 8150021 Work Modality Hybrid... ...Maywood-Health Sciences Campus Department Name HEMATOLOGY ONCOLOGY Location Code HEMATOLOGY - ONCOLOGY (06508A) Is...SuggestedHourly payFull timeWork experience placementLocal areaLoyola University
Chicago, IL3 days ago- The Biological Sciences Division at the University of Chicago is hiring a Clinical Research Coordinator II for managing comprehensive clinical trials in Hematology/Oncology. This role demands a Bachelor's degree and 2-5 years of related experience, focusing on subject...Suggested
- The University of Chicago's BSD MED - Hematology and Oncology is seeking a Clinical Research Coordinator 2 (CRC2) to partner with the PI and manage daily clinical trial activities, coordinating compliance, finances, personnel, and study documentation. Responsibilities...Suggested
$28 per hour
...Position Details Position Details Job Title CLINICAL RESEARCH COORDINATOR I Position Number 8151017 Work Modality Hybrid... ...Department Name CBCC Research Location Code HEMATOLOGY - ONCOLOGY (06508A) Is this split and/or fully grant funded?...SuggestedHourly payFull timeWork experience placementWork at officeLocal areaLoyola University
Maywood, IL5 days ago$55k - $65k
...Clinical Research Data Coordinator - Cancer Center Clinical Trials Office Search Extension until September... ...the review/audit process to ensure oncologic clinical trials can be conducted at... ...records and conduct of clinical hematology and oncology research studies a...SuggestedFull timeWork at officeWorldwideUniversity of Illinois
Chicago, IL16 days ago- The University of Chicago is seeking a Clinical Research Coordinator I for the BSD Hematology/Oncology - Clinical Research Staff, Cluster 9. The CRC1 will support multi-center cooperative group and pharmaceutical trials at national and intergroup levels, coordinating protocols...
- ...The Clinical Research Coordinator II (Denton, TX) will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The...
Dm Clinical Research Group
Melrose Park, IL2 days ago $60k - $75k
...Clinical Research Coordinator IIThe Clinical Research Coordinator II (CRC II) is an onsite, patient-facing, specialized researcher partnering with the clinical Principal Investigator (PI) and under the direction of the Clinical Research Manager. The CRC II supports, facilitates...Work experience placementUniversity of Chicago
Chicago, IL1 day ago$60k - $75k
...Clinical Research Coordinator II Cellular Manufacturing As a Clinical Research Coordinator II Cellular Manufacturing, you will work in a state-of-the-art cleanroom within the UChicago Cellular and Tissue-Based Processing cGMP Facility, supporting the manufacture of...Work experience placementWork at office$27.47 - $38.81 per hour
...offered for the position. Offers may vary depending on the circumstances of each case. Summary: Job Summary: The Clinical Research Coordinator II (CRC II) independently coordinates assigned aspects of clinical research studies across a range of disciplines....Hourly payFull timeLocal areaShift workWeekend workAfternoon shiftrush
Chicago, IL10 days ago$60k - $75k
...Department BSD SUR - Research Services: Clinical Research About the Department Since the founding of the Department in 1927, many... ...collaborative environment. Job Summary The Clinical Research Coordinator II (CRC2) is a specialized researcher working with the...Full timeWork experience placementThe University of Chicago
Chicago, ILmore than 2 months ago$60k - $75k
## Clinical Research Coordinator II - EndocrinologyApplyremote type: Onsitelocations: Hyde Park Campustime type: Full timeposted on: Posted Todayjob requisition id: JR34413**Department**BSD MED - Endocrinology - Pannain Research Staff**About the Department**The Section...Work experience placement- The Clinical Research Coordinator II (CRCII) at The University Of Chicago partners with the Principal Investigator in the Endocrinology section to recruit, consent, and monitor study participants, collect data and specimens, and ensure adherence to GCP and all regulatory...
- The Biological Sciences Division at the University of Chicago is seeking a Clinical Research Coordinator II to manage multiple clinical trials with a focus on compliance and data management. This role requires collaboration with principal investigators and study personnel...
- The Biological Sciences Division at the University of Chicago seeks a Clinical Research Coordinator II to support daily trial activities onsite, partnering with the PI and the Clinical Research Manager. The CRC II coordinates screening, enrollment, consent, data collection...
- The University of Chicago in Chicago, IL seeks a Clinical Research Coordinator II to partner with the PI and Clinical Research Manager in the Gastroenterology section of the Department of Medicine. The role involves coordinating multiple clinical trials, ensuring protocol...
- University of Chicago is seeking a Clinical Research Coordinator II to partner with the PI in endocrinology research. You will recruit and enroll participants, obtain consent, and monitor patient status while ensuring data integrity and regulatory compliance. The role...
- The University of Chicago's Biological Sciences Division, Endocrinology Section, seeks a Clinical Research Coordinator II to work with the PI Dr. Silvana Pannain. The CRCII will coordinate participant enrollment, data collection, and study logistics within NIH/academic...
- The University of Chicago in Chicago, IL seeks an onsite Clinical Research Coordinator II to support neurology clinical trials under the direction of the clinical PI and the Clinical Research Manager. You will handle screening, consent, data collection, adverse event reporting...
- The Clinical Research Coordinator II (CRC II) at Rush University Medical Center in Chicago coordinates assigned aspects of clinical research studies across disciplines, including recruitment, data management, regulatory submission, and sponsor communication. Responsibilities...
- Dm Clinical Research Group in Denton, TX seeks a Clinical Research Coordinator II to ensure quality data and adherence to sponsor protocols, FDA regulations and ICH/GCP guidelines. The role emphasizes enrollment targets and timely study conduct across assigned sites. Requirements...
- The Biological Sciences Division at the University of Chicago is seeking a Clinical Research Coordinator II to support the manufacture of clinical-grade cellular therapies and vaccines for Phase I-III trials. Responsibilities include performing aseptic processing, managing...Work experience placement
- Rush University Medical Center is seeking a Clinical Research Coordinator II to independently coordinate multiple clinical studies. You will recruit and retain participants, manage study data, and handle regulatory submissions with increasing autonomy. The role supports...
$27 - $31 per hour
A prominent educational institution in Chicago is seeking a Clinical Research Coordinator II to manage multiple research protocols efficiently. This role includes data collection, participant interaction, and compliance with regulations. The ideal candidate should possess...$60k - $75k
The University Of Chicago is seeking a Clinical Research Coordinator II in Chicago, IL. This role involves managing multiple clinical trials, recruiting participants, and ensuring compliance with protocols. The ideal candidate will have a Bachelor's degree and 2-5 years...- The University of Chicago is seeking a Clinical Research Coordinator II for Gastroenterology to manage all aspects of clinical trials in a high‑volume setting. You will screen, enroll, follow up with subjects, and ensure accurate data entry and adverse event reporting...
- Rush University Medical Center in Chicago is seeking a Clinical Research Coordinator II to independently coordinate assigned aspects of clinical research across disciplines. You will recruit and retain participants, manage study data, submit regulatory documents, and maintain...
- Rush University Medical Center is seeking a Clinical Research Coordinator II to independently coordinate assigned aspects of clinical studies across disciplines. The role emphasizes recruitment, data management, regulatory documentation, and liaison with sponsors and departments...
- The University of Chicago is seeking a Clinical Research Coordinator II - Cellular Manufacturing to work in a state-of-the-art cleanroom supporting the manufacture of clinical-grade cellular therapies for Phase I-III trials. You will perform aseptic processing, execute...
$49.92k - $81.62k
...Pediatric Clinical Research CoordinatorAnn & Robert H. Lurie Children's Hospital of Chicago provides superior pediatric care in a setting... ...requirements of each research program.Essential Job Functions:Coordinates and manages the initiation and regulatory compliance of...Hourly payFull timePart timeLurie Children's Hospital
Chicago, IL1 day ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Coordinator II - Hematology/Oncology. Be the first to apply!
Related searches
- clinical research coordinator Chicago, IL
- clinical project manager Chicago, IL
- global clinical trial manager Chicago, IL
- neuroscience clinical research coordinator Chicago, IL
- clinical trials manager Chicago, IL
- clinical research coordinator ii Chicago, IL
- sr. clinical trial manager Chicago, IL
- senior clinical trials manager Chicago, IL
- clinical research lead Chicago, IL
- clinical trials Chicago, IL