Our patients are our number one priority! We're committed to giving children back their childhood!

Job Posting Title:

Research Coordinator II

Location:

Dallas - Hospital

Additional Posting Details:

Monday - Friday

8:00am - 4:30pm

Job Description:

Duties/Responsibilities

Specific responsibilities will include, but not limited to the following:  

• Collaborate with staff in other research divisions and clinical departments within Scottish Rite to obtain the information and/or support necessary to conduct research. Organizes and able to conduct division or project meetings, research meetings with Principal Investigators and provides reports/updates on research studies and activities  

• Performs literature reviews, assists with actual study design, collection of information and resources, completes forms, and creates consent forms for the preparation of submissions for projects to the appropriate regulatory authorities or for presentation or publication purposes 

• Submission and organization of required documents to regulatory agencies including the Research Advisory Panel and Institutional Review Board including initial submissions, continuing reviews, modifications, and closures 

• Develop and maintain appropriate timelines for completion of projects. Communicates well with the team and promptly reports barriers or delays. Communicate with researchers to resolve issues in order to meet project milestones and deadlines 

• Execution of approved study protocols.  Adherence to all protocol requirements. Provides regular updates of status and promptly communicates any issues. Responsible for maintaining regulatory binder for internal or external audits. Manage reporting of any non-compliance (reportable events, adverse events, UPIRSOs, protocol deviations) as needed to internal and external regulatory boards.  

• Screen, recruit, obtain and document consent of study subjects. Notify appropriate staff of subject research recruitment 

• Take the lead with scheduling patients and procedures (may include clinic visits, questionnaires, lab draws, radiographs, photography, videotaping, gait studies or other assessments). Monitor clinical follow-up for research participants to ensure appointments are kept and any necessary testing is completed within time frames established in study protocol 

• Collect and record research data in a systematic, reliable, and accurate manner to ensure data integrity. Responsible for data management, record keeping, and database/registry maintenance.  

• Generate required reports and/or organizes data for statistical analysis 

• Involved in the preparation, editing and submission of abstracts, posters, lectures, PowerPoint presentations, manuscripts and/or funding opportunities for presentation and/or publications 

• Effectively conduct internal, industry-sponsored and IRB audits and evaluate, document and create plans and processe