Top 141704 Programs 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
Referral Coordinator
Gift of Life —Philadelphia, PA
- Full-time
- Bachelor of Science
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Quick Apply
Benefits Coordinator
HARTFORD ROMAN CATHOLIC DIOCESAN CORP —Bloomfield, CT
- Urgent Care
- Mid-level
- Office
11d
Clinical Research Coordinator
Paradigm Clinical Research Center —Modesto, CA
- $55,000 - $65,000 a year
- Part-time
- Background check
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
Quick Apply
Laboratory Sample Operations Coordinator
Lenox Executive Search —Cambridge, MA
- $32 - $38 an hour
- Contract
- Background check
- Mid-level
- 3 years
Quick Apply
14d
Data Management Coordinator
Holistic Industries —Pittsburgh, PA
- $26 - $34 an hour
- Remote
- Urgent Care
- Continuous improvement
- Organizational skills
- Store discount
- Health savings account
Quick Apply
Coordinator, Special Projects & Programs, Department of Radiology
University of Cincinnati —Cincinnati, OH
- Full-time
- Mid-level
- Office
- University
- Paid parental leave
- Paid holidays
Onboarding Coordinator
RCX Sports —Remote
- $50,000 - $52,000 a year
- Weekends as needed
- Remote
- Mid-level
- 3 years
- Bachelor's degree
- Paid parental leave
- Health insurance
Quick Apply
10d
Student Support Coordinator
eDynamic Learning —Remote
- $45,000 - $55,000 a year
- Full-time
- Remote
- Customer service
- Computer literacy
- Mid-level
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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
Quick Apply
Project Coordinator
Brault —Remote
- $26 - $32 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- Health insurance
- Dental insurance
HR Administrative Coordinator
Tonal —Remote
- $70,000 - $78,000 a year
- Temporary
- Remote
- Writing skills
- Mid-level
- Bachelor's degree
9d
Membership Coordinator
American Institute of Aeronautics and Astronautics —Reston, VA
- $55,000 - $65,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Office
- Bachelor's degree
- Health savings account
- Disability insurance
Quick Apply
Academic Programs Coordinator
University of California, Irvine —Irvine, CA
- $32.74 - $52.54 an hour
- Full-time
- Background check
- Google Workspace
- Writing skills
- Health insurance
- Retirement plan
Research Coordinator
University of Pennsylvania —Philadelphia, PA
- $44,500 - $46,108 a year
- Full-time
- Hybrid work
- Background check
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
Coordinator, Program
NATIONAL MATH AND SCIENCE INITIATIVE INC —Remote
- $25.10 - $28.87 an hour
- Full-time
- Remote
- Mid-level
- Continuous improvement
- Criminal background check
- Paid parental leave
- Paid holidays
Public Relations Coordinator (2026 Graduates Apply Here)
LaunchSquad —San Francisco, CA
- $46,000 - $50,000 a year
- Email
- Remote
- Customer service
- Research
- Communication skills
- Health insurance
- Dental insurance
Quick Apply
Regulatory Coordinator II (Remote)
Cedars-Sinai —Beverly Hills, CA
- $34.24 - $58.21 an hour
- 8 hour shift
- Remote
- HIPAA
- Mid-level
- 3 years
Client Support Coordinator
The Hilb Group —Remote
- $22 an hour
- Overtime
- Remote
- Microsoft Excel
- Administrative experience
- Analysis skills
- 401(k)
- Paid time off
10d
Client Success Coordinator
TechnologyAdvice —Remote
- $50,000 - $59,000 a year
- Remote
- Mid-level
- US work authorization
- Communication skills
- Paid parental leave
- AD&D insurance
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

programs coordinator jobs

Clinical Research Coordinator

Referral Coordinator

Benefits Coordinator

Clinical Research Coordinator

Laboratory Sample Operations Coordinator

Data Management Coordinator

Coordinator, Special Projects & Programs, Department of Radiology

Onboarding Coordinator

Student Support Coordinator

Grants Project Coordinator & Data Processing Specialist, Junior

Project Coordinator

HR Administrative Coordinator

Membership Coordinator

Academic Programs Coordinator

Research Coordinator

Coordinator, Program

Public Relations Coordinator (2026 Graduates Apply Here)

Regulatory Coordinator II (Remote)

Client Support Coordinator

Client Success Coordinator

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