Top 156 Local program coordinator Jobs in Des Moines, Ia

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
7d
DISABILITY ACCESS POINT COORDINATOR
Polk County, IA —Des Moines, IA
- $80,819 a year
- Writing skills
- Pass drug screening
- HIPAA
13d
Intake Coordinator
Innovive Health —Des Moines, IA
- $20 - $23 an hour
- Full-time
- Hybrid work
- Mid-level
- Home Health
- Experience equivalent to degree accepted
- Continuing education credits
- Mileage reimbursement
Quick Apply
13d
Energy Efficiency Program Coordinator
Resource Innovations —Des Moines, IA
- $21 - $22 an hour
- Full-time
- Microsoft Word
- Background check
- Microsoft Excel
- Commuter assistance
- Paid holidays
Quick Apply
5d
Safety Coordinator
Vessco Water —Des Moines, IA
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Customer service
- Health insurance
- Dental insurance
Quick Apply
14d
Program Planner II Victim Assistance Engagement Coordinator
State of Iowa —Des Moines, IA
- Full-time
- Inventory management
- Mid-level
- Presentation skills
13d
Benefit Coordinator
Kleinfelder Inc —West Des Moines, IA
- Full-time
- Background check
- HIPAA
- Mid-level
- Paid holidays
- Health insurance
9d
RN Manager of Health Services - Assisted Living
Luther Park Community —Des Moines, IA
- Full-time
- Nursing
- RN License
- BLS Certification
- Free parking
- Continuing education credits
Quick Apply
Commercial Project Superintendent
Beal Derkenne Construction —Des Moines, IA
- $80,000 - $110,000 a year
- Full-time
- CPR Certification
- Management
- OSHA
- Health insurance
- Dental insurance
Quick Apply
Maintenance Coordinator
Courtyard Estates at Hawthorne Crossing —Bondurant, IA
- $21 - $24 an hour
- Full-time
- Sanitation
- Mid-level
- Apartments
- Disability insurance
- Health insurance
Quick Apply
6d
Business Development - Sales Territory Representative
SMS —Des Moines, IA
- $100,000 - $110,000 a year
- Full-time
- Mid-level
- 3 years
- High school diploma or GED
- Health insurance
- Dental insurance
Quick Apply
2d
Wound Care Coordinator Registered Nurse
MercyOne —Des Moines, IA
- Full-time
- Nursing
- RN License
- Hospital
Quick Apply
CVSICU RN Evenings
MercyOne —Des Moines, IA
- 12 hour shift
- Nursing
- Medication administration
- RN License
Quick Apply
Cardiovascular Surgical RN Evenings (No Weekends)
MercyOne —Des Moines, IA
- Full-time
- Nursing
- Medication administration
- Surgery
Quick Apply
Neuro ICU RN
MercyOne —Des Moines, IA
- 12 hour shift
- Nursing
- Medication administration
- RN License
Quick Apply
Neuro ICU RN Days
MercyOne —Des Moines, IA
- 12 hour shift
- Nursing
- Medication administration
- RN License
Quick Apply
Neuro ICU RN Part Time
MercyOne —Des Moines, IA
- 12 hour shift
- Nursing
- Medication administration
- RN License
Quick Apply
Population Health Pharmacist
MercyOne —Des Moines, IA
- Full-time
- Bachelor of Science
- Research
- Bachelor's degree
Quick Apply
6d
Taste Ambassador Coordinator
Anderson Erickson Dairy —Des Moines, IA
- Part-time
- Hybrid work
- Background check
- Computer literacy
- Office
12d
Veterinary Patient Care Coordinator
Hubbell Animal Hospital —Des Moines, IA
- $17 - $19 an hour
- Full-time
- Computer literacy
- Mid-level
- High school diploma or GED
- Disability insurance
- Health insurance
Quick Apply

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local program coordinator jobs near des moines, ia

Clinical Research Coordinator

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

Quick Apply

Job Details

Full-time
7 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

local program coordinator jobs in des moines, ia

Clinical Research Coordinator

DISABILITY ACCESS POINT COORDINATOR

Intake Coordinator

Energy Efficiency Program Coordinator

Safety Coordinator

Program Planner II Victim Assistance Engagement Coordinator

Benefit Coordinator

RN Manager of Health Services - Assisted Living

Commercial Project Superintendent

Maintenance Coordinator

Business Development - Sales Territory Representative

Wound Care Coordinator Registered Nurse

CVSICU RN Evenings

Cardiovascular Surgical RN Evenings (No Weekends)

Neuro ICU RN

Neuro ICU RN Days

Neuro ICU RN Part Time

Population Health Pharmacist

Taste Ambassador Coordinator

Veterinary Patient Care Coordinator

I want to receive the latest job alert for local program coordinator in des moines, ia

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