Top 13112 Processing coordinator Jobs

Clinical Research Coordinator
Mission Cancer + Blood, part of University of Iowa Health Care —Waukee, IA
- Full-time
- Background check
- Nursing
- RN License
- Health insurance
- Dental insurance
Quick Apply
10d
Billing Coordinator
Hometown Health Centers —Schenectady, NY
- $20.00 - $29.50 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply
Enrollment Coordinator
HAMASPIK CHOICE INC —Spring Valley, NY
- $22 - $25 an hour
- Full-time
- Mid-level
- Quality control
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Regional Operations Coordinator
Confidential —Barnstable, MA
- $75,000 - $85,000 a year
- Full-time
- Mid-level
- Office
- Continuous improvement
- Paid holidays
- Health insurance
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13d
Hog Procurement Coordinator
Triumph Foods, L.L.C —Saint Joseph, MO
- Monday to Friday
- Microsoft Outlook
- Word processing
- Computer literacy
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Grants Project Coordinator & Data Processing Specialist, Junior
LCG, Inc. —Rockville, MD
- $23.49 - $29.31 an hour
- Remote
- Microsoft Outlook
- Customer service
- Administrative experience
- Paid holidays
- Disability insurance
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Grants Project Coordinator & Data Processing Specialist, Associate
LCG, Inc. —Rockville, MD
- $27.64 - $34.01 an hour
- Remote
- Microsoft Outlook
- Mid-level
- Continuous improvement
- Paid holidays
- Disability insurance
Quick Apply
Document Coordinator - Trident University International (Remote)
Trident University —Remote
- $13.24 - $22.12 an hour
- Remote
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Employee stock purchase plan
- Paid holidays
Quick Apply
Client Support Coordinator
The Hilb Group —Remote
- $22 an hour
- Overtime
- Remote
- Microsoft Excel
- Administrative experience
- Analysis skills
- 401(k)
- Paid time off
9d
Retirement Support Coordinator
The Hilb Group —Remote
- $22 an hour
- Part-time
- Remote
- Entry level
- 401(k)
- Paid time off
9d
Billing Coordinator - Cable Construction
Pirtano Construction —Itasca, IL
- $20 an hour
- Full-time
- Office
- Organizational skills
- In-person
- Health insurance
- Dental insurance
Quick Apply
Coordinator, Quality Documentation
Voyant Beauty —Holmdel, NJ
- Full-time
- Microsoft Excel
- Microsoft Outlook
- ERP systems
- Opportunities for advancement
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Accounts Receivable Coordinator
LHH US —Erlanger, KY
- $22 - $25 an hour
- Military encouraged
- Fair chance
- 1 year
- Commuter assistance
- Paid holidays
Quick Apply
Hybrid Clinical Research Coordinator
TEKBERRY —Stanford, CA
- $38 - $44 an hour
- Day shift
- Mid-level
- Data entry
- Organizational skills
- Health insurance
- Dental insurance
Quick Apply
2d
Marketing PO / Invoice Coordinator
Vaco by Highspring —Los Angeles, CA
- $37 - $38 an hour
- Temporary
- Microsoft Excel
- Mid-level
- Office
- Health insurance
- Dental insurance
Quick Apply
Billing Coordinator
Rose Villa —Portland, OR
- $24 - $28 an hour
- Part-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Free parking
- Employee discount
Quick Apply
13d
Data Coordinator
Cross Catholic Outreach —Remote
- $20.67 - $24.38 an hour
- Full-time
- Remote
- Background check
- Microsoft Outlook
- Customer service
- Paid parental leave
- Health savings account
Quick Apply
Payroll Coordinator
Shemmassian Academic Consulting —Remote
- $55,000 - $62,000 a year
- Full-time
- Remote
- Google Workspace
- Mid-level
- Administrative experience
- Health insurance
- Dental insurance
Quick Apply
2d
Travel Logistics Coordinator - Human Services Program - Remote
The Workforce Group —Remote
- $27 - $29 an hour
- Extended hours
- Remote
- Background check
- Spanish
- Pass drug screening
Quick Apply
14d
Security Onboarding Coordinator - Human Services Program - Remote
The Workforce Group —Remote
- Remote
- Background check
- Spanish
- Pass drug screening
Quick Apply

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Clinical Research Coordinator

Mission Cancer + Blood, part of University of Iowa Health Care -
Waukee, IA

Quick Apply

Job Details

Full-time
10 days ago

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Life insurance
Retirement plan

Qualifications

Clinical research
RN License
Employee relationship building
Clinical trials
CCRP

Full Job Description

Position Title: Clinical Research Coordinator

Summary: This position is responsible for organizing, planning and controlling work flow of all clinical research related activities. The Clinical Research Coordinator is required to have an in-depth knowledge of clinical trial requirements and good clinical practices as set forth by federal regulations. As the primary resource for the clinical trials, the coordinator will act as liaison between the investigators, the institutional review board (IRB), and the study sponsors. Along with the investigator, the research coordinator will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the research coordinator will be responsible for all data and source documentation, adverse experience reporting, and maintenance of complete regulatory files.

Essential Duties and Responsibilities include the following. Other duties may be assigned.

Communications / Liaison:

Maintain cooperative relationship with co-workers, component hospital departmental staff, investigator medical office staff, study sponsor contacts, and clinical research participants.
Answer telephone, screen calls, take messages, and provide information to appropriate staff.
Communicate on a regular basis with investigators and office nurses regarding the availability of clinical studies.
Act as liaison between investigators and study sponsor staff.
Maintain cooperative relationship with co-workers, component hospital departmental staff, investigator medical office staff, study sponsor contacts, and clinical research participants.
Attend component hospital Tumor Board conferences when assigned.
Communicate needs for laboratory, pathology, and/or radiology submissions.
Communicate investigational drug orders and schedules to designated pharmacist.

Screening and Enrollment:

Ascertain that there is documented IRB approval to the IRB for clinical trials prior to registration/randomization
Review the study design and inclusion/exclusion criteria with the investigator.
Review and verify all relevant source documentation in the subject's medical record to confirm study eligibility. Review the protocol, informed consent form, and follow-up procedures with potential study subjects if so directed by the investigator.
Ensure the current approved informed consent and HIPAA agreement form are signed before subjects are screened and enrolled.
Ensure that the registration/randomization procedure is followed as per protocol guidelines.
Document record of the subject's registration/randomization as well as data assigned and/or waived by the registering study sponsor.
Maintain accrual log and spreadsheet of protocol patients.
Enter registered/randomized subjects into database.
Calculate and verify protocol treatment drug dosages with a second CRA and the treating investigator.

Subject Follow-up:

Prepare, maintain, and distribute a subject calendar with treatment schedule, test schedule, and follow-up schedule to ensure adherence to protocol requirements.
Monitor dosage modifications and treatment calculations.
Obtain continuous follow-up information on subject's medical status per protocol.
Assess and record all adverse drug events as outlined in the protocol.
Report adverse drug events / attribution according to federal and study sponsor guidelines by completing required forms and online data submission.
Ensure appropriate specimen collection as required per protocol.

Data Management:

Collate data for submission to meet protocol requirements.
Abstract data from appropriate sources to complete case report forms.
Key data for remote data entry or submit completed case report forms per protocol guidelines.
Maintain source documentation for all case report form entries, including clinic chart visit notes, lab data, radiology reports, pathology reports, operative reports, and hospitalizations.
Ensure resolution of study sponsor queries in timely manner.
Review study sponsor delinquency reports for deficiencies.
Correct and edit case report forms, as appropriate.

Other:

Assist in training of all new CRAs, chemotherapy nurses, and investigator assigned nurses.
Assist Pharmacist in ordering investigational drugs, maintaining drug accountability records, and delivery of investigational drugs to satellite offices.
Assist in internal quality assurance program and routine monitoring audits.
Participate in presentations or seminars related to the field of clinical research.

Supervisory Responsibilities

This job has no supervisory responsibilities.

Qualifications:

Education and/or Experience:

Certified Clinical Research Professional, Registered Nurse, or B.S. in Health Related Field. Equivalent related work experience can be substituted for educational experience. Oncology and/or clinical research experience preferred. Computer experience in Database software, Internet software and Word Processing software preferred.
Frequent travel to local satellite offices is required. Occasional overnight travel to sponsor meetings is also required for training purposes and updates.

Job Type: Full-time

Benefits:

401(k)
Dental insurance
Health insurance
Life insurance
Paid time off
Retirement plan

Work Location: In person

Quick Apply

Refine Your Search

processing coordinator jobs

Clinical Research Coordinator

Billing Coordinator

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