Top 73 research scientist Jobs in omaha ne

Clinical Research Coordinator
UroHealth Partners —Omaha, NE
- Full-time
- CPR Certification
- Vital signs
- Patient monitoring
- Health insurance
- Dental insurance
Quick Apply
Mobile Clinical Research Nurse - Omaha, NE
Vita Mobile —Omaha, NE
- Day shift
- Patient monitoring
- RN License
- Mid-level
Quick Apply
12d
AI Research Scientist
Gallup —Omaha, NE
- $165,000 - $225,000 a year
- Hybrid work
- Azure
- Computer Science
- Mid-level
- Health insurance
- Dental insurance
Research Technician I (Part-Time)
University of Nebraska Medical Center —Omaha, NE
- $16.49 - $23.08 an hour
- Part-time
- Microsoft Outlook
- Computer literacy
- Basic math
Part-Time Researcher - Biomechanics
University of Nebraska at Omaha —Omaha, NE
- $22.50 an hour
- Part-time
- University
- Bachelor's degree
- Python
Researcher
University of Nebraska Medical Center —Omaha, NE
- $55,400 - $83,100 a year
- Full-time
- Microsoft Outlook
- Doctoral degree
- Computer literacy
14d
Clinical Research Coordinator
Nebraska Methodist Health System —Omaha, NE
- Full-time
- Anatomy knowledge
- BLS Certification
- HIPAA
Research Associate
Federal Reserve Bank of Kansas City —Omaha, NE
- $59,000 - $90,800 a year
- Full-time
- Mid-level
- Office
- Master's degree
7d
Research Assistant II
Boys Town National Research Hospital —Omaha, NE
- Part-time
- Bilingual
- Computer Science
- Basic math
- Health insurance
- Tuition reimbursement
4d
Research Scientist I- Institute for Human Neuroscience
Boys Town National Research Hospital —Omaha, NE
- Multiple hires
- Computer Science
- Hospital
- Office
- Health insurance
- Tuition reimbursement
Clinical Study Coordinator
University of Nebraska Medical Center —Omaha, NE
- $57,000 - $85,500 a year
- Full-time
- Microsoft Word
- 6 years
- Mid-level
1d
Field Research Technician—Temporary
University of Nebraska at Omaha —Omaha, NE
- $15 an hour
- Temporary
- Outdoor work
- Entry level
Clinical Research Associate I
University of Nebraska Medical Center —Omaha, NE
- $18.99 - $28.51 an hour
- Full-time
- Computer literacy
- Writing skills
- 3 years
2d
Food Scientist
Conagra Brands —Omaha, NE
- $63,000 - $93,000 a year
- Full-time
- Mid-level
- Office
- 3 years
- Employee stock purchase plan
- Health insurance
12d
Instructor
University of Nebraska Medical Center —Omaha, NE
- Online Application
- University
- Doctor of Philosophy
- Senior level
GME Administrative Research Associate
University of Nebraska Medical Center —Omaha, NE
- $23.17 - $34.76 an hour
- Full-time
- Microsoft Outlook
- Customer service
- Mid-level
Postdoctoral Research Associate
University of Nebraska Medical Center —Omaha, NE
- Full-time
- Office
- University
- Doctor of Philosophy
Clinical Research Coordinator II
Creighton University —Omaha, NE
- Full-time
- Blood sampling
- Computer literacy
- Mid-level
Quick Apply
Clinical Research Data Sr Associate
Nebraska Medicine —Omaha, NE
- Full-time
- Hybrid work
- Microsoft Access
- Microsoft Outlook
- Computer literacy
- Tuition reimbursement
- Opportunities for advancement
7d
Research Assistant I - The Language in the Environment (LITE) Lab
Boys Town National Research Hospital —Omaha, NE
- Part-time
- Bilingual
- Computer Science
- Writing skills
- Health insurance
- Tuition reimbursement
1d

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Clinical Research Coordinator

UroHealth Partners -
Omaha, NE

Quick Apply

Job Details

Full-time

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching
Flexible schedule
Life insurance
Retirement plan

Qualifications

CPR Certification
Vital signs
Clinical research
BLS Certification
Administrative experience
Medical administrative support
Certified Medication Aide
Nursing

Full Job Description

THIS POSITION IS 100% ONSITE, IN PERSON LOCATED IN OMAHA, NE

POSITION SUMMARY:

Under the direction and supervision of the Principal Investigator and administrator, this position facilitates all implementation phases of new studies as well as the ongoing coordination and maintenance of open and closed studies. The position arranges and oversees all clinical trial activities and plays a key role in assisting the Principal Investigator (PI) in recruiting patients for clinical studies. The position works closely with the Principal Investigator, members of the department, study sponsors and monitors, and the institution, to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of all ongoing clinical studies.

ESSENTIAL JOB FUNCTIONS/RESPONSIBILITIES:

1) Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

2) Schedules study participant appointments and serves as the patient liaison to the PI and other participating physicians.

3) Reviews and comprehends each assigned protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.

4) Working closely with the PI, participates in an integral way in the informed consent process by communicating clearly and openly with potential study patients about protocols open to enrollment. Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process.

5) Proficiently and efficiently perform various clinical procedures and assessments.

6) Coordinates and attends sponsor prequalification visits, monitor visits, study termination visits.

7) Completes case report forms. Extracts data from patient charts in a timely manner

8) Responds to data clarification requests in a timely manner.

9) May attend Investigator meetings requiring travel and report pertinent information back to research team members.

10) Coordinates with PIs and department to help ensure that clinical research and related activities are performed in accordance with Federal regulations, and sponsoring agency policies and procedures.

11) Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains records and other documentation of training.

12) Maintains subject screening logs and protocol deviation logs.

13) Maintains a spreadsheet tracking updates to database of all subjects enrolled on clinical trials.

14) Coordinates and facilitates monitoring and auditing visits. Notifies appropriate institutional officials of external audits by IRB’s, Regulatory agencies, CRO’s and sponsors.

15) Collaborates with PI and institution to respond to any audit findings and implement-approved recommendations.

16) Completes documentation on each study visit that is used to track all study related activities so that time, effort and materials can be accounted for on a monthly basis.

17) Ensures that all materials for each clinical trial protocol are available for subject enrollment.

18) Works collaboratively with the other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed and that there is timely documentation and submission of study data.

19) Performs specimen processing and shipment of biological specimen duties.

20) Assists with study materials including but not limited to, the informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs.

21) Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials as required.

22) Arranges secure storage of study documents that will be maintained according to institutional policy or for the contracted length of time, whichever is longer.

23) Other duties as assigned related to the billing practices, policies, and procedures.

24) Obtain patient vitals and phlebotomy.

25) Must work as a team member and perform actions consistent with established Urohealth Partners policies and procedures including standards for safety, attendance, punctuality and personal appearance. Perform other duties as assigned.

ESSENTIAL JOB REQUIRMENTS:

EDUCATION

· Registered Nurse or LPN license or other healthcare related field experience preferred

· Two years in a clinical research setting, preferably working as a clinical research coordinator on Industry-Sponsored clinical trials

CERTIFICATIONS

· CPR

· Medication Aide

· HIPAA Certification, preferred not required

EXPERIENCE

· Urology experience, preferred not required

· Two years of related work experience, preferred; or equivalent combination of experience and education.

Job Type: Full-time

Benefits:

401(k)
401(k) matching
Dental insurance
Flexible schedule
Health insurance
Life insurance
Paid time off
Retirement plan
Vision insurance

Experience:

Clinical research: 1 year (Required)

License/Certification:

Certified Medication Aide (Required)
BLS Certification (Required)

Work Location: In person

Quick Apply

Refine Your Search

research scientist jobs in omaha ne

Clinical Research Coordinator

Mobile Clinical Research Nurse - Omaha, NE

AI Research Scientist

Research Technician I (Part-Time)

Part-Time Researcher - Biomechanics

Researcher

Clinical Research Coordinator

Research Associate

Research Assistant II

Research Scientist I- Institute for Human Neuroscience

Clinical Study Coordinator

Field Research Technician—Temporary

Clinical Research Associate I

Food Scientist

Instructor

GME Administrative Research Associate

Postdoctoral Research Associate

Clinical Research Coordinator II

Clinical Research Data Sr Associate

Research Assistant I - The Language in the Environment (LITE) Lab

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