Clinical Research Coordinator I - Section of Behavioral Oncology

SHIFT:

Day (United States of America)

Seeking Breakthrough Makers

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A Brief Overview
My (Lisa Schwartz, PhD) NIH- and foundation-funded lab at CHOP (Center for Childhood Cancer Research, Section of Behavioral Oncology) focuses on self-management of adolescents and young adults (AYA) impacted by cancer (those with cancer predisposition, on active treatment, or survivors). Examples of areas of study include digital health interventions, decision-making, adherence, and physical activity.

Seeking a bachelors or masters level coordinator to:

Assist with management of multiple studies, including 1 multi-site study of AYA survivor self-management, and 1 study of interventions related to genetic testing for cancer predisposition among youth. Specific tasks include:

• Assist with participant recruitment and data collection in CHOP’s Cancer Center across
• multiple studies.
• Assist with tracking participants and managing related data.
• Collect data from electronic health records for screening participants and documenting
• medical/treatment variables.
• Code and manage qualitative data.
• Assist with preparation of grants and papers such as lit searches, writing/editing, using
• endnote for references.
• Help to oversee and mentor student research assistants.
• Help to develop protocols/manuals of procedures for studies.
• Help to manage and prepare all IRB related regulatory documents.

Background in psychology, public health, nursing, pre-medicine or other related fields preferred.

Candidate is expected to have prior clinical research experience and feel comfortable interacting in a medical setting with medical teams and medically compromised adolescents and young adults.

Although not necessary, the ideal candidate would have prior research experience in a medical setting, experience with SPSS, Endnote and Redcap, and experience with and comfort with digital health platforms.

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.

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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.

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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.