Clinical Research Coordinator – Safe Place Position Available In Philadelphia, Pennsylvania

Clinical Research Coordinator•Safe Place Children’s Hospital of Philadelphia United States, Pennsylvania, Philadelphia Jun 11, 2025

SHIFT:

Day (United States of America) Clinical Research Coordinator I Seeking Breakthrough Makers Children’s Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation. At CHOP, your experience is valued; your voice is heard; and your contributions make a difference for patients and families. Join us as we build on our promise to advance pediatric care-and your career. CHOP’s Commitment to Diversity, Equity, and Inclusion CHOP is committed to building an inclusive culture where employees feel a sense of belonging, connection, and community within their workplace. We are a team dedicated to fostering an environment that allows for all to be their authentic selves. We are focused on attracting, cultivating, and retaining talent who can help us deliver on our mission to be a world leader in the advancement of healthcare for children. We strongly encourage candidates of all races, colors, ethnicities, religions, perspectives, sexes, backgrounds, and lived experiences to apply.

A Brief Overview Safe Place:

The Center for Child Protection and Health and Clinical Futures at Children’s Hospital of Philadelphia are seeking a full-time or part-time bilingual research coordinator. The ideal candidate will have a Master’s Degree in a health related field and experience in patient-oriented research. The research coordinator will work multiple projects including a multicenter study evaluating the efficacy of a positive parenting intervention (PriCARE) and a multicenter child abuse pediatrics research network (CAPNET). Specific responsibilities include but are not limited to: 1) recruiting and consenting families, 2) conducting study interviews, 3) maintaining subject tracking system, 3) scheduling subjects for interviews, 4) conducting chart reviews and abstracting clinical data, 4) performing data quality checks.

JOB SUMMARY

This is a full-time or part-time Clinical Research Coordinator position offered through Clinical Futures at

Children’s Hospital and Safe Place:

The Center for Child Protection and Health in the Division of General Pediatrics at Children’s Hospital of Philadelphia. The Clinical Research Coordinator will assist the Principal Investigator in activities related to PriCARE and CAPNET. Under minimal supervision, the coordinator will facilitate all clinical research activities within the scope of the clinical research protocols. The coordinator will also be responsible for training and overseeing student research assistants. What you will do Position-specific responsibilities
Adhere to an IRB approved protocol and submit protocol amendments and updates as needed
Support data enterers and other team members at collaborating sites
Coordinate study intervention sessions (virtual or in-person) and childcare sessions (when in-person sessions are restarted)
Act as a liaison for research subject, investigator, IRB, sponsor, community partners, and healthcare professionals.
Core responsibilities
Submit protocol amendments and updates to the IRB as needed
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
Related responsibilities
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 Education High School Diploma / GED Required
Bachelor’s Degree Preferred Experience At least two (2) years of clinical or clinical related or research related experience Required
At least three (3) years of clinical or clinical related or research related experience Preferred Knowledge, Skills and Abilities 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
Bilingual in Spanish and English
Ability to perform assigned tasks independently and with minimal supervision.
Able to work accurately, work well with others, and pay strict attention to detail.
Work in collaboration with other professionals and staff.
Must be adaptable to do work which is varied and requires an intellectual and professional approach.
Requires a flexibility of skills and hours (some evening hours may be required)
Strong organizational skills
Efficient in navigating video conference platforms
REDCap knowledge and experience preferred, but not required
Excellent interpersonal skills and ability to converse professionally with families
Excellent oral and written communication skills
Experience with diverse, low-income, urban families through prior work, volunteer, or other experience
Familiarity with statistical software, such as Stata or R, is preferred but not required.
Strong interest in and commitment to public health research, program implementation, and child health policy that aims to improve outcomes for children and families.
Willingness to commit at least 1 year to the position To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community. As a condition of employment, professionals working onsite•at any CHOP location, for any portion of time•must be vaccinated for

COVID-19.

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SALARY RANGE

$51,730.00•$64,660.00 Annually Salary ranges are shown for full-time jobs. If you’re working part-time, your pay will be adjusted accordingly.•At CHOP, we are committed to fair and transparent pay practices. Factors such as skills and experience could result in an offer above the salary range noted in this job posting. Click here for more information regarding CHOP’s Compensation and Benefits.