Clinical Research Data Sr Associate

Shift:

Shift Details:

M-F 8am - 5pm

Hybrid after training.

Why Work at Nebraska Medicine?

• Together. Extraordinary. Join a team that values your skills, delivering exceptional care through collaboration.
• Leading Health Network Work with the region's top academic health network, partnering with UNMC to transform lives through education, research, and patient care.
• Diversity and Inclusion We value diverse backgrounds and experiences, reflecting the communities we serve.
• Educational Support Enjoy up to $5,000/year in tuition assistance, a 35% discount at Clarkson College, and career advancement opportunities with covered educational costs. Enjoy support for your personal growth within the organization, from those just starting their healthcare careers to those who are years down the path.

Be part of something extraordinary at Nebraska Medicine!

Responsible for the collection and review of clinical protocol research and registry data. Interpret data (including appropriate source documentation) for entry into computerized databases. Creates tools related to data collection for clinical research conducted by investigators. Provide support to Blood and Marrow Transplant and Cellular Therapy program through data collection, research protocol management, and other clinical research duties. Manage stem cell donor search requests. Maintain and communicate donor search progress to the clinical team. Negotiate and coordinate procurement of donor stem cell products in accordance with the patient's transplant timeline. Coordinate internal unrelated donor collections with clinical team, serving as a liaison between donor, Donor Center and the NMDP.

Required Qualifications:

* Minimum of one year data collection or data management experience required.

* High school education or equivalent required.

* Bachelor's degree in health science or related field or equivalent combination of education/experience combined (One year of experience equals one year of education) required.

* Proficient in Microsoft Office including Excel and Word required.

* Excellent organizational skills required. Ability to prioritize multiple tasks/responsibilities required.

* Knowledge of clinical research and records review required.

* Good verbal and written communication skills required.

* Computer literacy required. Ability to work effectively with other team members required.

* Strong interpersonal skills required.

Preferred Qualifications:

* Oncology/hematology experience preferred.

* Experience and/or knowledge of clinical trials and registry preferred.

* Prior experience working with physicians preferred.

* Bachelor's degree in health science or related field preferred.

* Experience with web based data entry systems (MediData, RAVE) preferred.

* Knowledge of medical terminology preferred. Database system knowledge preferred.

* Experience with Microsoft Access, PowerPoint, and Outlook preferred.

* Knowledge of Epic EMR preferred.