Top 184 Field coordinator Jobs in West 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
8d
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
Clinic Director (BCBA) ***$15,000 Signing Bonus***
Stride Autism Centers —Des Moines, IA
- $90,000 - $95,000 a year
- Full-time
- Management
- Clinic experience
- Mid-level
- Continuing education credits
- Paid parental leave
Quick Apply
Scheduling Coordinator
Chicago Tube And Iron Company —Ankeny, IA
- Full-time
- Microsoft Outlook
- Basic math
- Mid-level
Quick Apply
RN Appointment Coordinator Pediatric (Full-Time)
ChildServe —Johnston, IA
- Full-time
- Experience working with individuals with developmental disabilities
- CPR Certification
- Nursing
- Health insurance
- Dental insurance
Quick Apply
Supply Chain Coordinator
Accelera —Ankeny, IA
- $26.13 - $30.25 an hour
- Full-time
- Mid-level
- Bachelor's degree
- Business Administration
Quick Apply
9d
Youth Treatment Counselor
Orchard Place —Des Moines, IA
- $18 - $21 an hour
- Full-time
- Mid-level
- 3 years
- High school diploma or GED
- Loan forgiveness
Quick Apply
Regional Marketing Field Coordinator
Lennar —Des Moines, IA
- $20.05 - $25.00 an hour
- Full-time
- Inventory management
- Computer literacy
- Bachelor of Science
- Paid parental leave
- Health insurance
Leasing Field Coordinator
Renters Warehouse LLC —Urbandale, IA
- $50,000 a year
- Full-time
- Clean driving record
- Mid-level
- Office
Quick Apply
13d
Health Improvement Coordinator
State of Iowa —Des Moines, IA
- Full-time
- Background check
- Nursing
- Mid-level
- Paid holidays
- Disability insurance
14d
Program Planner II Victim Assistance Engagement Coordinator
State of Iowa —Des Moines, IA
- Full-time
- Inventory management
- Mid-level
- Presentation skills
14d
Assistant Project Coordinator
Boyd Jones Construction —Urbandale, IA
- Part-time
- Organizational skills
- Business
- Associate's degree
Quick Apply
Recreation Lead
City of Clive (IA) —Clive, IA
- $19 - $25 an hour
- Seasonal
- Computer literacy
- Mid-level
- Ability to lift 50 pounds
6d
Product Compliance Coordinator
Merchants Bonding Company —West Des Moines, IA
- Full-time
- Experience equivalent to degree accepted
- Business Administration
- 1 year
Quick Apply
6d
AMP Program Coordinator
YSS —Des Moines, IA
- $20.74 - $25.92 an hour
- Full-time
- Bilingual
- Background check
- Management
- Health savings account
- Paid holidays
Organ Recovery Coordinator
Iowa Donor Network —Altoona, IA
- $64,200 - $80,200 a year
- Weekends as needed
- Anatomy knowledge
- Surgery
- Writing skills
Quick Apply
Event Coordinator
Blank Park Zoo —Des Moines, IA
- Weekends as needed
- Word processing
- Mid-level
- Ability to lift 50 pounds
Bookkeeper/Administrative Assistant
Larson Development —Johnston, IA
- $25 - $35 an hour
- Part-time
- Word processing
- Mid-level
- Office
Quick Apply
Recruiting Coordinator
Ruan Transportation Management Systems —Des Moines, IA
- High school diploma or GED
- Communication skills
- Entry level
- Disability insurance
- Health insurance
Quick Apply
Construction Coordinator - Elec Ops
MidAmerican Energy Company —Adel, IA
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Construction site
6d

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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
8 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

field coordinator jobs in west des moines ia

Clinical Research Coordinator

Commercial Project Superintendent

Clinic Director (BCBA) $15,000 Signing Bonus

Scheduling Coordinator

RN Appointment Coordinator Pediatric (Full-Time)

Supply Chain Coordinator

Youth Treatment Counselor

Regional Marketing Field Coordinator

Leasing Field Coordinator

Health Improvement Coordinator

Program Planner II Victim Assistance Engagement Coordinator

Assistant Project Coordinator

Recreation Lead

Product Compliance Coordinator

AMP Program Coordinator

Organ Recovery Coordinator

Event Coordinator

Bookkeeper/Administrative Assistant

Recruiting Coordinator

Construction Coordinator - Elec Ops

I want to receive the latest job alert for field coordinator in west des moines ia

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