Top 95168 Educations Program Coordinator Jobs

Clinical Research Coordinator
Knowledge Research Center —Orange, CA
- $72,000 - $78,000 a year
- Full-time
- Background check
- Vital signs
- Ability to walk for extended periods
- Health insurance
- Dental insurance
Quick Apply
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Physician - DO / MD - Webster, MA - Great Pay, Great benefits, Schedule M-F 8:30 - 5:00 PM - Great Job!
Fallon Health —Webster, MA
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RN Care Coordinator
Scenic Rivers Health Services —Bigfork, MN
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MBK Senior Living —Klamath Falls, OR
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Nemours —Wilmington, DE
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Interborough Developmental and Consultation Center —Brooklyn, NY
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Registered Nurse
Lincoln Street Inc. —Springfield, VT
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Radiologic Technologist (Multiple schedule options available)
Olympia Orthopaedic Associates —Olympia, WA
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X-Ray Technician (Multiple schedule options available)
Olympia Orthopaedic Associates —Olympia, WA
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PACE Medical Director, Jordan Valley Senior Care
Jordan Valley Health —Springfield, MO
- Full-time
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Maintenance Manager
TreeHouse Foods —Cambridge, MD
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- Engineering
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Special Procedure Technologist - IR/Angio
Ellis Medicine —Schenectady, NY
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MRI Technologist
Olympia Orthopaedic Associates —Olympia, WA
- $50.00 - $65.08 an hour
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RN PACU Charge Nurse
Legent Health —Plano, TX
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Home Health and Hospice Clinical Manager
BETHESDA HEALTH AND HOUSING —Willmar, MN
- $74,719.54 - $84,146.34 a year
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CNA Instructor - RN
Wisconsin Illinois Senior Housing Inc. WISH Home Office —Merrill, WI
- $40 an hour
- Full-time
- Classroom
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Clinical Research Coordinator

Knowledge Research Center
Orange, CA

Quick Apply

Job Details

Full-time
$72,000 - $78,000 a year

Benefits

Health insurance
Dental insurance
Paid time off
Vision insurance
401(k) matching
Life insurance

Qualifications

Certified Phlebotomy Technician
Clinical research
Phlebotomy specimen handling

Full Job Description

JOB SUMMARY:

The Clinical Research Coordinator works independently providing study coordination including

Coordinate and manage clinical trial activities in compliance with study protocols, ICH-GCP guidelines, FDA regulations, and IRB requirements.
Recruit, screen, consent, and follow up with study participants
Conduct informed consents with study participants
Responsible for oversight of all assigned studies
Plans and coordinates strategies for increasing research participant enrollment, improving efficiency.
Schedule and conduct study visits, including data and sample collection.
Maintain accurate source documentation, regulatory binders, and case report forms.
Prepare, submit, and maintain regulatory documents for IRB and sponsor submissions.
Ensure timely reporting of adverse events, deviations, and essential documents.
Act as a primary point of contact for study monitors, sponsors, and investigators.

ESSENTIAL JOB DUTIES AND RESPONSIBILITIES:

Manages the clinical research portfolio and daily operations of studies for the investigator or disease group.
Independent study coordination including screening of potential research participants for protocol eligibility.
presenting non-medical trial concepts and details to the research participants and participating in the informed consent process.
Scheduling of research participants for research visits and procedures.
In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in research participant condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
Maintains accurate source documents related to all research procedures.
Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries.
Schedules and participates in monitoring and auditing activities.
Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
Notifies direct supervisor about concerns regarding data quality and study conduct.
Works directly with the Institutional Review Board (IRB) to submit initial applications, amendments, continuing reviews, Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
May involve other regulatory / Institutional Review Board duties
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
Maintains research practices using Good Clinical Practice (GCP) guidelines.
Maintains strict research participant confidentiality according to HIPAA regulations and applicable law.
Participates in required training and education programs.
At least 2 years of clinical research experience; experience in liver studies strongly preferred.
Perform study procedures, including phlebotomy, vital signs, and specimen processing.
Current phlebotomy certification and proficiency in blood draws required.
Strong organizational skills and attention to detail.
Plans and coordinates strategies for increasing research participant enrollment, and/or improving clinical research efficiency.
Excellent communication and interpersonal skills for working with patients, physicians, and sponsors.
Identifies new research opportunities and presents to investigators.
Organizes routine research meetings.

EDUCATION AND EXPERIENCE REQUIREMENTS:

Education:

BA/BS degree.

Certification/License:

Phlebotomy Certification

Experience:

Two years minimum of directly related experience.

EDUCATIONAL AND WORK EXPERIENCE PREFERENCES:

PHYSICAL REQUIREMENTS (physical abilities essential to perform the job):

Able to perform moderate lifting. Able to sit, stand and walk for prolonged periods of time.
Able to read papers and online documents. Able to operate standard office equipment.
Able to exercise physical ability and perspective acuity to satisfactorily perform essential job functions.

Job Type: Full-time

Pay: $72,000.00 - $78,000.00 per year

Benefits:

401(k) matching
Dental insurance
Health insurance
Life insurance
Paid time off
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

Educations Program Coordinator jobs

Clinical Research Coordinator

Coordinator, Data Operations

Registered Nurse Care Manager - Clinical Diabetes Educator; $30,000 Sign On, $15,000 Relocation, and Retention Bonus eligible

Physician - DO / MD - Webster, MA - Great Pay, Great benefits, Schedule M-F 8:30 - 5:00 PM - Great Job!

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Registered Nurse (RN)

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Staff Development Coordinator (RN)

Radiologic Technologist (Multiple schedule options available)

X-Ray Technician (Multiple schedule options available)

PACE Medical Director, Jordan Valley Senior Care

Maintenance Manager

Special Procedure Technologist - IR/Angio

MRI Technologist

RN PACU Charge Nurse

Home Health and Hospice Clinical Manager

CNA Instructor - RN

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