Clinical Research Coordinator

PeopleAdmin, Inc.; Omaha (NE); On-site; USD 52,000 - 70,000; Full time

Job summary

University of Nebraska Medical Center in Omaha is seeking a qualified professional to support the evaluation, startup, activation, and closeout of clinical studies in rheumatology. You will manage study operations from launch through completion, coordinating with sponsors and clinical teams to ensure timelines and regulatory compliance.

This role emphasizes data integrity, collaboration, and attention to detail to advance novel therapies and improve patient outcomes in rheumatologic conditions.

Qualifications

• Bachelor's degree or equivalent required.
• Two years related experience in clinical or laboratory research preferred.
• Experience in data collection and data management is required.

Responsibilities

• Manage operational aspects of assigned studies from launch to closeout.
• Collaborate with sponsors, internal departments, and regulatory partners to meet timelines and compliance.

Skills

Data entry

Data management

Interpersonal skills

Communication skills

Independent work

Judgment and decision making

Education

Bachelor's degree or equivalent

Health Science or related field

Tools

Microsoft Excel

Microsoft Word

Microsoft Access

SAS

SPSS

STATA

Job description

UNMC is an Equal Employment Opportunity Employer, including an equal opportunity employer of protected veterans and individuals with disabilities.

Location

Omaha, NE

Department

Int Med Rheumatology 50000594

Business Unit

College of Medicine

Reg-Temp

Full-Time Regular

Work Schedule

As directed by supervisor

Remote/Telecommuting

No remote/telecommuting opportunity

Position Summary

Work closely with Rheumatology Principal Investigators (PIs) to support the evaluation, feasibility, startup, activation, coordination, and closeout of clinical studies— with a primary focus on groundbreaking gene and cellular therapy trials at the University of Nebraska Medical Center.

As a key contributor to the research mission, you will manage all operational aspects of assigned studies from launch through completion. You’ll collaborate with study sponsors, internal departments, Nebraska Medicine clinical teams, and regulatory partners to ensure timelines, study requirements, and compliance standards are met. This position offers the opportunity to directly impact the advancement of novel therapies and improve outcomes for patients with rheumatologic conditions.

Required and Preferred Qualifications

Required Education

Bachelor's degree or equivalent

Health Science or related field (Will consider six years related education and/or experience combined of which two years must include related post high school education)

Required Experience

2 years

Experience in a clinical or laboratory research setting to include data collection and/or data management experience (Will consider six years related education and/or experience combined of which two years must include related post high school education)

Required License

No

Required Computer Applications

Microsoft Excel, Microsoft Word

Required Additional Knowledge, Skills and Abilities

Hands on computer experience, specifically in the areas of data entry and data management. A premium will be placed on flexibility, good interpersonal and communication skills in addition to willingness to learn. Able to design, plan, and implement research projects. The ability to work independently, while exercising judgment and decision-making skills.

Preferred Education

Health related field

Preferred License

No

Preferred Computer Applications

Microsoft Access, Microsoft Outlook, SAS, SPSS

Preferred Other Computer Applications

STATA

Preferred Additional Knowledge, Skills and Abilities

Library research skills, medical database searches and retrieval, as well as internet research.

Individuals who need accommodation during the online application or interview process may contact 402-559-4070 or [e-mail] to request an accommodation.