Clinical Research Coordinator I - Neonatology

Responsibilities

Adhere to an IRB approved protocol

Participate in the informed consent process of study subjects

Support the safety of clinical research patients/research participants

Coordinate protocol related research procedures, study visits, and follow-up care

Screen, recruit and enroll patients/research participants

Maintain study source documents

Under the supervision of PI Report adverse events

Understand good clinical practice (GCP) and regulatory compliance

Educate subjects and family on protocol, study intervention, etc

Comply with Institutional policies, standard operating procedures (SOPs) and guidelines, and with HIPAA and management of confidential materials

Must comply with federal, state, and sponsor policies

For multi-site studies or collaborations, support communication and meeting scheduling across teams

Manage essential regulatory documents

Register study on ClinicalTrials.gov as appropriate

Complete case report forms (paper & electronic data capture) and address queries

Submit documents to regulatory authorities (e.g. IRB, FDA, etc.) and/or review/monitoring boards (ie,DSMB, independent safety officer)

Facilitate pre-study, site qualification, study initiation, and monitoring visit as appropriate

Facilitate study close out activities as appropriate

Coordinate research/project team meetings

Collect, process and ship samples as applicable to the protocol

Schedule subject visits and procedures

Retain records/archive documents after study close out

Preferred

Bachelor's Degree

At least three (3) years of clinical or research related experience

Glassdoor

3.9

Since its start in 1855 as the nation's first hospital devoted exclusively to caring for children, The Children's Hospital of Philadelphia has been the birthplace for many dramatic firsts in pediatric medicine.

Philadelphia, Pennsylvania, USA

http://chop.edu

H1B Sponsorship

Data Powered by

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Education and Training

Engineering and Development

Customer Service and Support

Management and Executive

Arts and Entertainment

Legal and Compliance

Creatives and Design

Trends of Total Sponsorships

*2026

Qualifications

High School Diploma / GED

At least two (2) years of clinical or research related experience

Basic knowledge of IRB and human subject protection

Strong verbal and written communications skills

Strong time management skills

Ability to collaborate with stakeholders at all levels

Bachelor's Degree

At least three (3) years of clinical or research related experience

Required skills

Represents the skills you have, click on the tags, IRB and Human Subject Protection, Stakeholder Collaboration

Preferred skills

Bachelor's Degree, Glassdoor, 3.9, Philadelphia, Pennsylvania, USA, http://chop.edu, H1B Sponsorship, Data Powered by, Distribution of Different Job Fields Receiving Sponsorship, Represents job field similar to this job, Education and Training, Engineering and Development, Customer Service and Support, Management and Executive, Arts and Entertainment, Legal and Compliance, Creatives and Design, Trends of Total Sponsorships, *2026, (94), 2025, (174), 2024, (166), 2023, (139), 2022, (114), 2021, (70), 2020

Experience

2+ years