Clinical Research Coordinator II- Orthopedics

Nemours Children's Health; Wilmington (DE); On-site; USD 65,000 - 85,000; Full time

Job summary

Nemours Children's Health is seeking a Clinical Research Coordinator II in Wilmington, DE to coordinate and complete orthopedic clinical research studies. You will assist in regulatory documents, educate families, recruit participants, and maintain study data and records.

The role involves coordinating with sponsors, participating in monitoring visits, and aiding in audits, with opportunities for mentoring junior coordinators and advancing in regulatory expertise.

Qualifications

• Bachelor’s degree in medical or science related field required.
• 3-5 years research experience.
• Clinical Research Coordinator certification or eligible to sit for exam; minimum 2 years coordination experience.
• Effectively uses Microsoft Office suite.
• Demonstrates ability to coordinate and establish priorities among diverse tasks.
• Effectively communicates verbally and in writing.

Responsibilities

• Coordinate and implement clinical research studies and trials in Orthopedics.
• Prepare regulatory documents and assist in IRB submissions and audits.
• Recruit, screen, and enroll study participants and obtain consent.
• Schedule and conduct study procedures and data collection; maintain study records and databases.
• Interfacing with sponsors and participating in monitoring visits and audits.
• Mentor new clinical research coordinators and train staff.

Skills

Communication skills

Coordination

Prioritization

Mentoring

Education

Bachelor’s degree in medical or science related field

Tools

Microsoft Office

Job description

Job Description

Nemours is seeking a Clinical Research Coordinator to join our Nemours Children's Health team in Wilmington, DE.

Nemours is seeking a Clinical Research Coordinator to join our Nemours Children's Health team in Wilmington, DE.

The Clinical Research Coordinator II coordinates, implements and completes clinical research studies and/or clinical trials in the Orthopedics Department at Nemours Children's Hospital Delaware by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and conducting study procedures, collecting and recording study data, maintaining detailed study records, interfacing with study sponsors, participation in sponsor study monitoring visits, prepare for and participate in internal and external research audits, maintain various research databases.

• Follows all aspects of Standard Operating Procedures and Good Clinical Practices in the conduct of clinical research; collects and prepares documents as required by sponsoring agencies; attends Investigator Meetings, as assigned;
• Understands and can conduct clinical research studies that require but not limited to, DSMB, Emergent Access, Conduct Investigator Initiated studies, Multi-site clinical trials, Research Team training manuals.
• Achieves clinical research coordinator certification from ACRP or SOCRA.
• Develops source documents, parental permission and assent documents for submission to IRB. Coordinates IRB submissions for assigned studies, maintains regulatory documents during conduct of study; develops and utilizes study participant and family teaching tools for study purposes; interfaces with representatives of sponsoring agencies.
• Participates in the conduct of parental permission/assent process for assigned studies; schedules study visits with study participants in accordance with study protocols; develops strategies to assure compliance of study participants with protocol requirements.
• Performs clinical data gathering and measurements and monitoring of data integrity, including data completeness, accuracy and quality. Maintains study databases
• Mentors new clinical research coordinators. Participates in training nursing and ancillary study staff for study purposes; recruits, screens and enrolls sufficient number of study participants in conformance with protocol requirements.
• Assists in identifying, reporting and following-up on Serious Adverse Events.
• Assists in the maintenance of study medication accountability records; prepares clinical specimens for shipment to central laboratories.
• Coordinates monitoring activities with Sponsors representative(s). Completes Case Report Forms; responds to sponsor queries, prepares for audits by sponsor, IRB and/or the FDA/DHHS.

Requirements

• Bachelor’s degree in medical or science related field required
• 3-5 years research experience
• Clinical Research Coordinator certification or eligible to sit for exam and a minimum of 2 years clinical research coordination experience
• Effectively uses Microsoft computer software
• Demonstrates ability to coordinate and establish priorities among diverse tasks
• Effectively communicates verbally and in writing

About Us

Nemours Children's Health is an internationally recognized pediatric health system serving more than 1.7 million patient encounters each year. We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.

Backed by the Nemours Foundation and Alfred I. duPont Trust, our $1.7B nonprofit system is dedicated to improving children's health through clinical care, research, education, advocacy, and prevention. Our Whole Child Health approach focuses equally on prevention and treatment, partnering with communities to help every child thrive.

Inclusion and belonging guide our strategy and growth. We are committed to culturally relevant care, reducing health disparities, and fostering an environment where every associate, patient, and family feels supported and valued.

Learn more at Nemours.org .