Top 13 Research coordinator Jobs in Omaha Ne

Clinical Research Coordinator
Confidential —Omaha, NE
- $24 - $29 an hour
- Full-time
- Background check
- Writing skills
- Clinic experience
- Health savings account
- Health insurance
Quick Apply
2d
Data Coordinator II, Clinical Research
University of Nebraska Medical Center —Omaha, NE
- $55,400 - $83,100 a year
- Full-time
- Hybrid work
- Microsoft Access
- Microsoft Outlook
- 5 years
8d
Clinical Research Coordinator
Nebraska Methodist Health System —Omaha, NE
- Full-time
- Anatomy knowledge
- BLS Certification
- HIPAA
Clinical Study Coordinator
University of Nebraska Medical Center —Omaha, NE
- $57,000 - $85,500 a year
- Full-time
- Microsoft Access
- 6 years
- Microsoft Outlook
Research Nurse Coordinator
University of Nebraska Medical Center —Omaha, NE
- $73,400 - $110,100 a year
- Full-time
- Hybrid work
- Microsoft Word
- Nursing
- Microsoft Outlook
Regulatory Coordinator I
University of Nebraska Medical Center —Omaha, NE
- $55,400 - $83,100 a year
- Full-time
- Hybrid work
- 6 years
- Microsoft Outlook
- Mid-level
Research Nurse Coordinator - LPN
University of Nebraska Medical Center —Omaha, NE
- $57,000 - $85,500 a year
- Weekends as needed
- Microsoft Word
- Nursing
- Microsoft Outlook
Research Nurse Coordinator, Lead
University of Nebraska Medical Center —Omaha, NE
- $73,400 - $110,100 a year
- Full-time
- Hybrid work
- Microsoft Word
- Nursing
- Microsoft Outlook
10d
Senior Tissue Procurement Coordinator
Live On Nebraska —Omaha, NE
- 12 hour shift
- Nursing
- Mid-level
- Driver's License
- Paid time off
- Retirement plan
Quick Apply
LPN Study Coordinator I
University of Nebraska Medical Center —Omaha, NE
- $48,200 - $72,300 a year
- Full-time
- Hybrid work
- Vital signs
- Microsoft Outlook
- Pediatrics
14d
Clinical Study Nurse Coordinator
University of Nebraska Medical Center —Omaha, NE
- $73,400 - $110,100 a year
- Full-time
- Hybrid work
- Microsoft Word
- Nursing
- RN License

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Clinical Research Coordinator
Confidential —Omaha, NE
Experience working with clinical trials, observational studies, registries, or sponsor-led research studies. Recruit, screen, and enroll qualified participants…
$24 - $29 an hour
Quick Apply
2d
Clinical Research Social Media & Participant Recruitment Specialist
QCR-Austin —Omaha, NE
This individual will create and manage digital content, develop social media recruitment campaigns, respond to potential participants, track recruitment leads,…
$26.40 - $32.00 an hour
Quick Apply
7d

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This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…
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Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…

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Clinical Research Coordinator

Confidential
Omaha, NE

Quick Apply

Job Details

Full-time
$24 - $29 an hour
2 days ago

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Vision insurance
Life insurance

Qualifications

Research laboratory experience
Regulatory documents
Interpersonal skills
Phlebotomy
Writing skills
Clinic experience
Phlebotomy specimen handling
Research project coordination
Clinical data entry
Attention to detail
Data entry
Research compliance clinical trial records management
Organizational skills
Implementing research protocols
Patient recruitment
Productivity software
Clinical quality assurance standards
Clinical confidentiality policies
Documentation Handling
Time management
Research compliance quality assurance records management

Full Job Description

Clinical Research Coordinator

Location: Omaha NE
Position Type: Full-Time, On-Site

We are seeking a professional, organized, and motivated Clinical Research Coordinator to join our Omaha office. The ideal candidate will have strong clinical research experience, excellent communication skills, and the ability to manage study-related activities while providing a positive experience for participants.

This role requires hands-on experience with phlebotomy and participant recruitment for clinical studies. Candidates must be comfortable engaging with potential participants, supporting enrollment goals, and performing blood draws as part of study protocols.

Key Responsibilities

The Clinical Research Coordinator will be responsible for coordinating day-to-day clinical research activities in accordance with study protocols, regulatory requirements, and company procedures. Responsibilities include:

Recruit, screen, and enroll qualified participants for clinical research studies
Conduct study visits and ensure protocol requirements are followed accurately
Perform phlebotomy/blood draws as required by study protocols
Obtain and document informed consent
Collect, enter, and maintain accurate study data and source documentation
Communicate with participants regarding study visits, requirements, and follow-up
Coordinate with investigators, sponsors, monitors, and internal team members
Maintain regulatory binders and study records
Support participant retention and ensure a professional, respectful participant experience
Follow Good Clinical Practice guidelines and applicable regulatory standards

Required Qualifications

Previous experience as a Clinical Research Coordinator or in a similar clinical research role
Phlebotomy experience is required
Experience recruiting participants for clinical research studies is required
Ability to perform blood draws confidently and safely in accordance with protocol and site procedures
Experience screening, enrolling, and retaining clinical research participants
Strong understanding of clinical research workflows and study visit coordination
Knowledge of Good Clinical Practice guidelines and regulatory documentation standards
Strong computer skills, including experience with electronic data capture systems, Microsoft Office, and electronic records
Excellent verbal and written communication skills
Strong organizational skills and attention to detail
Ability to manage multiple priorities and meet deadlines
Professional, dependable, and able to work independently and as part of a team
Ability to maintain confidentiality and handle participant information appropriately

Preferred Qualifications

Phlebotomy certification preferred
Experience working with clinical trials, observational studies, registries, or sponsor-led research studies
Experience with laboratory specimen processing, shipping, and chain-of-custody procedures
Experience with participant recruitment databases, community outreach, or prescreening campaigns

Physical Requirements and Work Environment

The physical demands described below are representative of those that must be met by an employee to successfully perform the essential functions of this position, with or without reasonable accommodation.

While performing the duties of this job, the employee may be required to:

Stand, walk, sit, bend, reach, stoop, and move throughout the clinic for extended periods of time
Sit at a desk and use a computer, phone, and office equipment for extended periods of time
Stand for extended periods during participant visits, clinical procedures, specimen handling, and study preparation
Use hands and fingers to handle clinical supplies, perform phlebotomy, process specimens, and operate equipment
Lift, carry, push, or pull clinical supplies, study materials, files, and equipment weighing up to 25
Assist with moving, organizing, and stocking study supplies and laboratory materials
Communicate clearly in person, by phone, and in writing
Work in a clinical environment where exposure to blood, bodily fluids, needles, laboratory specimens, and infectious materials may occur
Follow all required safety procedures, use appropriate personal protective equipment, and comply with infection control standards

Schedule and Location

This is a full-time, on-site position based in our Detroit, Michigan office. Regular attendance and punctuality are essential. Some schedule flexibility may be required depending on study visits, participant availability, sponsor requirements, or protocol needs.

Relocation assistance is not provided for this position.

Equal Employment Opportunity Statement

We are an Equal Opportunity Employer. We are committed to providing equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, pregnancy, national origin, age, disability, genetic information, veteran status, marital status, sexual orientation, gender identity, or any other characteristic protected by applicable federal, state, or local law.

Reasonable Accommodation

Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions of the position, unless doing so would create an undue hardship.

Additional Statement

This job description is intended to describe the general nature and level of work being performed. It is not intended to be an exhaustive list of all duties, responsibilities, or qualifications associated with the position. Duties may be modified at any time based on business needs, study requirements, or operational priorities.

How to Apply

Qualified candidates are encouraged to submit their resume for consideration. Please include details regarding your clinical research experience, phlebotomy experience, and study recruitment experience

Pay: $24.00 - $29.00 per hour

Benefits:

401(k)
Dental insurance
Health insurance
Health savings account
Life insurance
Vision insurance

Experience:

Phlebotomy: 1 year (Required)
Clinical Research : 1 year (Required)
Recruitment for clinical research participants : 1 year (Preferred)

Location:

Omaha, NE 68114 (Required)

Shift availability:

Day Shift (Required)

Work Location: In person

Quick Apply

Refine Your Search

research coordinator jobs in omaha ne

Clinical Research Coordinator

Data Coordinator II, Clinical Research

Clinical Research Coordinator

Clinical Study Coordinator

Research Nurse Coordinator

Regulatory Coordinator I

Research Nurse Coordinator - LPN

Research Nurse Coordinator, Lead

Senior Tissue Procurement Coordinator

LPN Study Coordinator I

Clinical Study Nurse Coordinator

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