Administrative and Data Coordinator

Nemours-Children; Orlando (FL); On-site; USD 32,000 - 52,000; Full time

Job summary

Nemours is seeking an Administrative and Data Coordinator in Orlando to provide administrative, secretarial, and technical support to the Clinical Trials Manager and Research Core. The role includes patient scheduling, registration tasks, and Greenphire management, with duties extending to minutes and data-related responsibilities.

The successful candidate will support staff meetings, manage calendars, maintain data files, and assist in special projects.

Qualifications

• Associate's degree required.
• 6 months to 1 year of relevant experience required.

Responsibilities

• Provide administrative, secretarial, and technical support to the Clinical Trials Manager and Research Core.
• Coordinate and manage calendars and scheduling; handle phone and email communications.
• Take meeting minutes and serve as recording assistant for staff meetings.
• Maintain and organize data files and spreadsheets; assist with data-related tasks.

Education

Associate's degree

Job description

Nemours is hiring an Administrative and Data Coordinator in our Research Department. The primary function is to provide administrative, secretarial, and technical support to the Clinical Trials Manager andthe Clinical Research Core on a daily basis. Job duties include but are not limited to: Patient scheduling, registration and Greenphire management.

Work in concert with other members of the research core team in relation to administrative and regulatory functions.Coordinate and act as recording assistant for staff meetings. Act as research backup support to research coordinators and assistants during times of absence or when needed for larger functions. The Administrative and Data Coordinator will have reporting responsibilities to the Clinical Trials Manager.

Primary Responsibilities:

1. Day-to-day support to Clinical Trials Manager, Research Clinical Coordinators and Research Clinical Assistants, other duties as needed; prioritize and work independently
2. Responsible for managing calendar for assigned persons
3. Confidentiality in all aspects of the position
4. Receive/field and initiate phone calls and other communications using verbal, written and electronic media; receive visitors
5. Maintenance and typing of data files and spreadsheets; filing and photocopying
6. Complete special projects at the direction of the Clinical Trials Manager.
7. Travel arrangements, reimbursements, and arrange special functions accommodations
8. Take minutes and serve as recording assistant for staff meetings
9. Meet regularly with supervisor and other members of the department as needed to receive and disseminate pertinent information and discuss issues of relevance.

Qualifications:

• Associate's degree required
• 6 months to a year of relevant experience required