Clinical Research Associate I: Study Coordination & IRB

University Of Nebraska Medical Center; Omaha (NE); On-site; USD 42,000 - 60,000; Full time

Job summary

University of Nebraska Medical Center in Omaha, NE, is seeking a Research Associate to coordinate IRB submissions, recruit participants, conduct study visits, and manage data collection. The role emphasizes accuracy, organization, and collaboration within a multidisciplinary team.

The ideal candidate has a strong work ethic, experience in healthcare or clinical research, and the ability to follow study protocols with attention to detail.

Qualifications

• Required Education: High School education or equivalent.
• Experience related to healthcare, laboratory and/or clinical research is preferred.
• Ability to work independently and as part of a team; accurate data entry and adherence to study protocols.

Responsibilities

• Coordinate IRB submissions and approvals for research studies.
• Recruit participants and conduct study visits following protocols.
• Collect and manage study data; ensure timely submission to sponsors.
• Collaborate with multidisciplinary teams to ensure study milestones are met.

Skills

IRB coordination

Data collection

Participant recruitment

Study visits

Team collaboration

Education

High School diploma

3 years related education/experience

Job description

University of Nebraska Medical Center in Omaha, NE, is seeking a Research Associate to coordinate IRB submissions, recruit participants, conduct study visits, and manage data collection. The role emphasizes accuracy, organization, and collaboration within a multidisciplinary team.

The ideal candidate has a strong work ethic, experience in healthcare or clinical research, and the ability to follow study protocols with attention to detail.