Team Lead Research Coordinator- General Hematology & Hemostasis and Thrombosis

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Work Shift

Day

Work Day(s)

Monday-Friday

Shift Start Time

8:00 AM

4:30 PM

Regular

Children’s is one of the nation’s leading children’s hospitals. No matter the role, every member of our team is an essential part of our mission to make kids better today and healthier tomorrow. We’re committed to putting you first, and that commitment is at the heart of our company culture: People first. Children always. Find your next career opportunity and make a difference doing what you love at Children’s.

Provides oversight for all aspects of clinical research occurring within the specified program and training and mentoring for clinical research personnel at site. Provides guidance and assistance in protocol development, serving as back-up coordinator to provide ongoing support for all trials in the specified program as needed. Communicates all relevant policy and procedure updates/revisions as directed by Manager, Research. Provides routine auditing/monitoring of ongoing trials for quality assurance purposes.

Experience

• 4 years of experience in clinical research or 3 years of experience in clinical research with advanced degree

Preferred Qualifications

• 2 years of experience in supervising staff
• Experience in creating and negotiating study budgets
• Experience in financial management
• Advanced degree

Education

• Bachelor’s degree in a scientific or health-related field

Certification Summary

• Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA) Certified Research Associate (CRA), Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or comparable within 1 year of employment
• ARUP Handling, Packaging and Shipping Infectious Substances or similar within 30 days of employment if role requires specimen acquisition.
• Collaborative Institutional Training Initiative (CITI) within 30 days of employment

Knowledge, Skills and Abilities

• Broad knowledge of federal regulations and regulatory requirements for conducting research with the ability to mentor
• Self-directed and motivated to work independently toward short- and long-term goals
• Good communication, organization, and interpersonal skills

Job Responsibilities

Develops, conducts, and facilitates research protocols at an expert level

• Collaborates with manager to assess data management needs.

• Assists with development of source and case report form tools.

• Provides back-up data entry services and ensures data integrity.

• Assists with participant screening, enrollment, study activities, and communication.

• Provides substantial support to investigators in writing study protocols.

• Ensures protocol feasibility within ancillary departments.

• Works collaboratively with manager to monitor metrics.

• Manages a large or multiple smaller clinical trial projects.

• Administers various research surveys in accordance with research study requirements.

• Assists with identifying suitable grants for investigators.

• Identifies and completes research gran