Oncology RN Research Coordinator 1 Job at Nuvance Health
Nuvance Health Norwalk, CT 06850
$31.25 - $58.05 an hour
Nuvance Health has a network of convenient hospital and outpatient locations — Danbury Hospital, New Milford Hospital, Norwalk Hospital and Sharon Hospital in Connecticut, and Northern Dutchess Hospital, Putnam Hospital Center and Vassar Brothers Medical Center in New York — plus multiple primary and specialty care physician practices locations, including The Heart Center, a leading provider of cardiology care, and two urgent care offices. Non-acute care is offered through various affiliates, including the Thompson House for rehabilitation and skilled nursing services, and the Home Care organizations.
Summary:
The Oncology Research Coordinator supports the WCHN oncology research program and coordinates all aspects of research subjects care during their trial participation (with an emphasis on the screening, enrollment, and monitoring of patient candidates/participants). The Coordinator will be committed to supporting the department's program's mission of conducting quality clinical research for our sponsors while providing safe and compassionate care to our patients. Works with physicians, the network oncology research manager and site directors, other research staff and allied health professionals to coordinate clinical research efforts provided at WCHN.
Responsibilities:
1. Independently conducts procedures related to screening, eligibility, consent, registration, patient education, and data collection for cancer clinical trials.
2. Prepares and submits to the IRB (Institutional Review Board) all required IRB documentation in a timely manner: including but not limited to new trial approval, sponsor submitted adverse events(SAE) information, annual updates, consent changes, and any patient SAE.
3. Performs patient assessment and chemotherapy toxicity evaluation based on NCI CTCAE criteria for adverseevents on treatment days and as needed.
4. Collaborates with oncology physician practices and staff to assure protocol compliance and scheduling of patient visits.
5. Tracks and enters clinical data on all cancer patients as required to include active patients and those in follow up in clinical trials.
6. Participates in investigator, coordinator or study initiation meetings. Assists with scheduling, reviewing clinical trial outline/content and preparing for monitor visits/audits with regulatory agencies or sponsors.
7. Provides education to staff on cancer clinical trials through in-services, writtne materials and one to one interaction for each study, each patient and general marketing.
8. Participates in oncology research meetings and multi-disciplinary case conferences.
9. Identifies potential patients for clinical trial eligibility.
10. Demonstrates flexibility in daily routine and effectively accommodates for the need of the job.
11. Fulfills all compliance responsibilities related to the position.
12. Performs other duties as assigned.
Other information:
Required: Oncology nursing and chemotherapy/biotherapy administration. Knowldege of current standardized cancer reporting criteria; performance status, adverse event grading and tumor assessment. MS Word and Excel. Demonstrates knowledge and understanding of GCP guidelines and regulatory requirements to maintain patient safety, confidentiality, and the integrity of the clinical trial process. Excellent interpersonal communication skills and attention to detail. Conducts screening, eligibility, patient education, and data collection for cancer clinical trials.
Minimum Experience: three years
Desired: Certification in Research. OCN-Oncology certified nurse, and ONS Chemotherapy/Biotherapy certification desired.
Location: Norwalk-34 Maple St
Work Type: Full-Time
Standard Hours: 40.00
FTE: 1.000000
Work Schedule: Day 10
Work Shift: 7am-5:30-pm
Org Unit: 396
Department: Cancer Research
Exempt: Yes
Grade: S10
Salary Range:
$31.2500 - $58.0500 Hourly
Working conditions:
Essential:
We will endeavor to make a reasonable accommodation to the known physical or mental limitations of a qualified applicant with a disability unless the accommodation would impose an undue hardship on the operation of our business. If you believe you require such assistance to complete this form or to participate in an interview, please contact Human Resources at 203-739-7330 (for reasonable accommodation requests only). Please provide all information requested to assure that you are considered for current or future opportunities.
Please Note :
chrismaxcer.com is the go-to platform for job seekers looking for the best job postings from around the web. With a focus on quality, the platform guarantees that all job postings are from reliable sources and are up-to-date. It also offers a variety of tools to help users find the perfect job for them, such as searching by location and filtering by industry. Furthermore, chrismaxcer.com provides helpful resources like resume tips and career advice to give job seekers an edge in their search. With its commitment to quality and user-friendliness, Site.com is the ideal place to find your next job.
Summary:
The Oncology Research Coordinator supports the WCHN oncology research program and coordinates all aspects of research subjects care during their trial participation (with an emphasis on the screening, enrollment, and monitoring of patient candidates/participants). The Coordinator will be committed to supporting the department's program's mission of conducting quality clinical research for our sponsors while providing safe and compassionate care to our patients. Works with physicians, the network oncology research manager and site directors, other research staff and allied health professionals to coordinate clinical research efforts provided at WCHN.
Responsibilities:
1. Independently conducts procedures related to screening, eligibility, consent, registration, patient education, and data collection for cancer clinical trials.
2. Prepares and submits to the IRB (Institutional Review Board) all required IRB documentation in a timely manner: including but not limited to new trial approval, sponsor submitted adverse events(SAE) information, annual updates, consent changes, and any patient SAE.
3. Performs patient assessment and chemotherapy toxicity evaluation based on NCI CTCAE criteria for adverseevents on treatment days and as needed.
4. Collaborates with oncology physician practices and staff to assure protocol compliance and scheduling of patient visits.
5. Tracks and enters clinical data on all cancer patients as required to include active patients and those in follow up in clinical trials.
6. Participates in investigator, coordinator or study initiation meetings. Assists with scheduling, reviewing clinical trial outline/content and preparing for monitor visits/audits with regulatory agencies or sponsors.
7. Provides education to staff on cancer clinical trials through in-services, writtne materials and one to one interaction for each study, each patient and general marketing.
8. Participates in oncology research meetings and multi-disciplinary case conferences.
9. Identifies potential patients for clinical trial eligibility.
10. Demonstrates flexibility in daily routine and effectively accommodates for the need of the job.
11. Fulfills all compliance responsibilities related to the position.
12. Performs other duties as assigned.
Other information:
Required: Oncology nursing and chemotherapy/biotherapy administration. Knowldege of current standardized cancer reporting criteria; performance status, adverse event grading and tumor assessment. MS Word and Excel. Demonstrates knowledge and understanding of GCP guidelines and regulatory requirements to maintain patient safety, confidentiality, and the integrity of the clinical trial process. Excellent interpersonal communication skills and attention to detail. Conducts screening, eligibility, patient education, and data collection for cancer clinical trials.
Minimum Experience: three years
Desired: Certification in Research. OCN-Oncology certified nurse, and ONS Chemotherapy/Biotherapy certification desired.
Location: Norwalk-34 Maple St
Work Type: Full-Time
Standard Hours: 40.00
FTE: 1.000000
Work Schedule: Day 10
Work Shift: 7am-5:30-pm
Org Unit: 396
Department: Cancer Research
Exempt: Yes
Grade: S10
Salary Range:
$31.2500 - $58.0500 Hourly
Working conditions:
Essential:
- Some manual skills / motor coord & finger dexterity
- Some occupational risk
- Sedentary/light effort. May exert up to 10 lbs. force
- Generally pleasant working conditions.
We will endeavor to make a reasonable accommodation to the known physical or mental limitations of a qualified applicant with a disability unless the accommodation would impose an undue hardship on the operation of our business. If you believe you require such assistance to complete this form or to participate in an interview, please contact Human Resources at 203-739-7330 (for reasonable accommodation requests only). Please provide all information requested to assure that you are considered for current or future opportunities.
Please Note :
chrismaxcer.com is the go-to platform for job seekers looking for the best job postings from around the web. With a focus on quality, the platform guarantees that all job postings are from reliable sources and are up-to-date. It also offers a variety of tools to help users find the perfect job for them, such as searching by location and filtering by industry. Furthermore, chrismaxcer.com provides helpful resources like resume tips and career advice to give job seekers an edge in their search. With its commitment to quality and user-friendliness, Site.com is the ideal place to find your next job.