Job Details

Company Overview

Shriners Children's is an organization that respects, supports, and values each other. We are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.

All employees are eligible for medical, dental and vision coverage on their first day! In addition, upon hire all employees are eligible for a 403(b) and Roth 403 (b) Retirement Saving Plan with matching contributions of up to 6% after one year of service. Employees in a full-time or part-time status (40+ hours per pay period) will also be eligible for paid time off, life insurance, short term and long-term disability and the Flexible Spending Account (FSA) plans. Additional benefits available to full-time and part-time employees include tuition reimbursement, home & auto, hospitalization, critical illness, pet insurance and much more! Coverage is available to employees and their qualified dependents in accordance with the plans. Benefits may vary based on state law.

Job Overview

The Clinical Research Coordinator is a research professional who ensures oversight and compliance of both system-wide and local clinical research activities. Works collaboratively with research personnel to ethically recruit and consent pediatric subjects and to appropriately collect and safeguard data. Overall, the Clinical Research Coordinator is the site's primary liaison among research participants, the local investigator(s) and study sponsors. The position's main responsibilities are to help ensure proper study conduct, subject safety, and the quality of data and data safeguards.

Responsibilities

• Supports the investigator's development of SHC investigator initiated research protocols
• Supports the implementation of approved research protocols
• Ensures studies are conducted in compliance with the approved protocol, Good Clinical Practice guidelines, applicable regulatory requirements, SHC policies and standards
• Responsible for tracking all aspects of projects including all study, investigator and IRB information, patient recruitment activity and financial management
• Coordinates the collection, statistical analysis and dissemination of data results throughout a clinical study
• Safeguards all participants involve din a research study support and approved by the organization
• Facilitates the local site's research programs and projects through collaborative, timely communication and teamwork

This is not an all-inclusive list of this job's responsibilities. The incumbent may be required to perform other related duties and participate in special projects as assigned.

**Note - this is a grant-funded position with three shifts per week up to 24 hours per week - core hours M-F between 8 a.m.-4:30 p.m.

Qualifications

Education

Bachelors degree in clinical research, science or other healthcare related field preferred. Without a Bachelors degree, 5 or more years of specific job-related experience in the administration of clinical research is required.

Master's degree in clinical research, science or other healthcare related field preferred

Certification/Licensure

Professional Licensure (e.g. nursing, PT, OT)

CCRP or CCRC certification preferred

Experience

Three or more years of clinical research experience required (site management, study management, IRBs, and federal regulations regarding clinical research compliance)