Clinical Research Coordinator I - Supportive Care in Oncology Research (SCORe)

Our take on this role

About this role

Coordinate clinical research projects in the Supportive Care in Oncology Research program focused on infectious complications associated with cellular therapy. Responsibilities include study visits, informed consent participation, participant education, and study documentation.

What could you bring from clinical work?

• Nurses and social workers: Experience explaining sensitive care information to patients and families could help you participate in the study informed consent process.
• OTs, PTs and SLPs: Your work educating patients and families about interventions may help you explain study protocols and interventions to participants and families.

Full job description from Children's Hospital of Philadelphia

SHIFT:
Day (United States of America)

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 does not discriminate on the basis of race, color, sex, national origin, religion, or any other legally protected categories in any employment, training, or vendor decisions or programs. CHOP recognizes the critical importance of a workforce rich in varied backgrounds and experiences and engages in ongoing efforts to achieve that through equally varied and non-discriminatory means. A Brief Overview The Supportive Care in Oncology Research (SCORe) program is seeking an energetic, organized, detail-oriented candidate. This position will support a Principal Investigator leading clinical and translational research focused on infectious complications associated with cellular therapy. The mission of the SCORe program is to conduct rigorous clinical and translational research that generates evidence to advance the prevention and treatment of infections. Through this work, the program aims to inform best practices and improve the health of children.
This role functions independently in a clinical research setting and is responsible for the complete coordination of specific clinical research projects, including clinical trials, observational, and data studies. This individual should have an interest in research related to the microbiome, infectious diseases, and viral illness in malignant and non-malignant transplant patients. This individual will perform all clinical research coordinator responsibilities, as detailed in the job responsibilities, working in collaboration with disease specific groups within the Center for Childhood Cancer Research (CCCR), Pediatric Infectious Disease Epidemiology & Antimicrobial Stewardship (IDEAS) group, and the Center for Microbial Medicine (CMM).
This role substantially coordinates all clinical research activities within the scope of clinical research protocols. Duties involve managing the day-to-day activities of the research study under the guidance of managing study staff and PI. What you will do
Core 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
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 Qualifications
High School Diploma / GED Required
Bachelor's Degree Preferred
Experience Qualifications
At least two (2) years of clinical or research related experience Required
At least three (3) years of clinical or research related experience Preferred
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
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, CHOP employees who work in patient care buildings or who have patient facing responsibilities must receive an annual influenza vaccine. Learn more. EEO / VEVRAA Federal Contractor | Tobacco Statement

SALARY RANGE:

$53,000.00 - $66,300.00 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.