Top 57 Clinical nurse coordinator Jobs in Ankeny 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
12d
Health & Wellness Coordinator
Centered Care —Urbandale, IA
- $35 - $40 an hour
- Full-time
- Background check
- Nursing
- RN License
- Health savings account
- Health insurance
Quick Apply
Wellness Director
StoryPoint —Ankeny, IA
- Weekends as needed
- Travel
- Senior level
- Leadership
- Health insurance
- Dental insurance
Quick Apply
Health & Wellness Coordinator
Centered Care —Ames, IA
- $38 - $40 an hour
- Part-time
- Background check
- Nursing
- RN License
- Health savings account
- Health insurance
Quick Apply
Wellness Director
StoryPoint —Des Moines, IA
- Weekends as needed
- Mid-level
- Travel
- Leadership
- Health insurance
- Dental insurance
Quick Apply
11d
Wound Care Coordinator Registered Nurse
MercyOne —Des Moines, IA
- Full-time
- Nursing
- RN License
- Hospital
Quick Apply
Patient Logistics RN Transfer Center Nights
MercyOne —Des Moines, IA
- Part-time
- Microsoft Word
- RN License
- Hospital
Quick Apply
LPN- Assistant Director of Nursing
Addington Place of Des Moines —Des Moines, IA
- Full-time
- Nursing
- Mid-level
- LPN
- Paid holidays
- Health insurance
Quick Apply
Wellness Director
Independence Village —Waukee, IA
- Weekends as needed
- Mid-level
- Travel
- Leadership
- Health insurance
- Dental insurance
Quick Apply
4d
Part Time Clinical Nursing Faculty
Chamberlain University —Des Moines, IA
- 12 hour shift
- Classroom
- Nursing
- Doctoral degree
Quick Apply
Nurse Practitioner or Physician Assistant - $5k Sign On Bonus
Curana Health —Des Moines, IA
- $110,000 - $120,000 a year
- Full-time
- Nursing
- Clean driving record
- Skilled nursing facility
- Disability insurance
- Health insurance
11d
RN- Clinical Coordinator Cardiac
MercyOne —Des Moines, IA
- Full-time
- Nursing
- RN License
- Hospital
2d
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
Clinical Research Assistant
INNOVO RESEARCH INC —Des Moines, IA
- Weekends as needed
- Computer literacy
- Clinic experience
- High school diploma or GED
- Disability insurance
- Health insurance
Quick Apply
Clinic Nurse- Blank Endocrinology Clinic
UnityPoint Health —Des Moines, IA
- Full-time
- Nursing
- RN License
- Customer service
- Paid holidays
- Disability insurance
Nurse Coordinator - Employee Health
UnityPoint Health —West Des Moines, IA
- Full-time
- Nursing
- RN License
- Hospital
- Paid holidays
- Disability insurance
1d
Infection Prevention Coordinator - RN
MercyOne —Des Moines, IA
- Full-time
- Acute care
- Nursing
- Hospital
- Vision insurance
Registered Nurse Clinical Coordinator
DAVITA —Ames, IA
- Weekends as needed
- Microsoft Word
- CPR Certification
- Nursing
- Paid training
- Health insurance
Plasma Center Nurse- RN
Biolife Plasma Services —Des Moines, IA
- $33.44 - $45.98 an hour
- Part-time
- CPR Certification
- Nursing
- RN License
- Paid holidays
- Disability insurance
9d
ASC Managing Director
Ankeny Medical Park Surgery Center —Ankeny, IA
- No weekends
- Surgery
- Current TB test
- RN License
- Profit sharing
- Health insurance

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clinical nurse coordinator jobs near ankeny ia

Clinical Research Coordinator

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

Quick Apply

Job Details

Full-time
12 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

clinical nurse coordinator jobs in ankeny ia

Clinical Research Coordinator

Health & Wellness Coordinator

Wellness Director

Health & Wellness Coordinator

Wellness Director

Wound Care Coordinator Registered Nurse

Patient Logistics RN Transfer Center Nights

LPN- Assistant Director of Nursing

Wellness Director

Part Time Clinical Nursing Faculty

Nurse Practitioner or Physician Assistant - $5k Sign On Bonus

RN- Clinical Coordinator Cardiac

Intake Coordinator

Clinical Research Assistant

Clinic Nurse- Blank Endocrinology Clinic

Nurse Coordinator - Employee Health

Infection Prevention Coordinator - RN

Registered Nurse Clinical Coordinator

Plasma Center Nurse- RN

ASC Managing Director

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