Lead Clinical Research Coordinator

Company Description

Sunbright Health Medical Centers in Homestead, FL is dedicated to bringing the ultimate patient-centered care environment to the community. Our team is committed to exceeding the expectations of patients, families, caregivers, support persons, guests, co-workers, physicians, and others. We value professionalism, dedication, expertise, honesty, ethics, and a commitment to innovation and excellence.

Role Description

We are seeking a highly motivated and results-driven Lead Research Coordinator to join our dynamic team.

The position will be full-time on-site, being responsible for conducting day-to-day research activities, coordinating data collection, and ensuring compliance with Institutional Review Board (IRB) regulations.

Collect, manage and analyze preliminary data using SPSS statistical software.

Coordinate patient screening and intake as well as educated patients about inform consent and drug accountability.

Create and present PowerPoint slides for training webinars, meetings, and conferences.

Oversee research program and ensure all elements of the program are in compliance with FDA regulations.

Create a process for FDA hold import shipments, in order so items will not be used.

Review and interpret IRB approve research protocols and consents for assign studies in order to support enhance patient care service.

Administer testing materials to patients and neurologically intact subjects to obtain research results.

Adhere to HIPAA guidelines regarding the sensitive and confidential nature of participant information.

Maintain security and confidentiality under HIPPA, GCP, study and institutional human research regulations.

Collaborate with principal investigators and internal and external customers for effective execution of clinical trials in an oncology clinic setting

Qualifications

Good Clinical Practice

IATA

Transporting Dangerous Goods

Analytical Skills, Research, and Data Collection

Excellent communication and presentation skills

Knowledge of Institutional Review Board (IRB) processes and regulations

Attention to detail and ability to organize and prioritize tasks

Experience in research settings

Bachelor's degree in a relevant field (e.g., healthcare, life sciences, psychology) is preferred.

Experience in organizing, and leading a team of coordinators from study start to finish.

Master's degree in a relevant field is a plus.

Job Type: Full-time

Benefits:

Flexible schedule

Paid time off

Experience level:

6 years

Schedule:

8 hour shift

Work Location:

In person