Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
ML
Methodist Le Bonheur Healthcare
Research Data Specialist |Trauma | Le Bonheur | Full-Time | Days
Career Insights for Data Specialist
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Tennessee data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Data Specialist uses software to store and organize data, such as an organization's records or financial information. Facilitates user and client access to information stored in databases. Ensures accuracy and efficient maintenance of data.
$61,498 / year median in Tennessee
+10% projected growth
Job Description
If you are looking to make an impact on a meaningful scale, come join us as we embrace the Power of One! We strive to be an employer of choice and establish a reputation for being a talent rich organization where Associates can grow their career caring for others. For over a century, we've served the health care needs of the people of Memphis and the Mid-South. Assists study team (Principal Investigator, Clinical Research Coordinator) in the collection, coordination, processing of all research related data. Maintains research protocol information, regulatory documents and other research files as applicable. Schedules and assists with sponsor monitoring visits and participant study visits. Models appropriate behavior as exemplified in MLH Mission, Vision and Values. Working at MLH means carrying the mission forward of caring for our community and impacting the lives of patients in every way through compassion, a deliberate focus on service expectations and a consistent thriving for excellence. A Brief Overview Assists study team (Principal Investigator, Clinical Research Coordinator) in the collection, coordination, processing of all research related data. Maintains research protocol information, regulatory documents and other research files as applicable. Schedules and assists with sponsor monitoring visits and participant study visits. Models appropriate behavior as exemplified in MLH Mission, Vision and Values. What you will do Works with investigators and coordinator on completion of case report forms; ensures timely data submission in accordance with SOP, CTA and protocol. Responsible for filing and maintaining all study related regulatory documents. Coordinates activities related to sponsor monitoring visits and ensures all follow up issues from monitoring visits are resolved in a timely manner with SOP and sponsor requirements. Schedules participants study visit and assists in screening potential research participants for studies. Assists with collection, processing and shipping of specimens, imaging documents or other items required for research purposes. Ensures packaging and shipment according to appropriate guidance and regulations. Maintains adequate clinical supplies according to study protocols. Maintains proficient knowledge of institutional and departmental guidelines, Federal regulations and Good Clinical Practice guidelines and relevant aspects of study protocols. Performs other job functions as assigned or requested Education/Formal Training Requirements Required
- High School Diploma or Equivalent Preferred
- Associates Degree Work Experience Requirements Required
- Medical or business office environment 1-3 years Knowledge, Skills and Abilities Knowledge of data collection, data entry, and data management Ability to communicate with physicians, clinical associates, patients and their families both verbally and in writing.
- exerting up to 25 lbs.