Clinical Research Assistant I - Hematology

Children's Hospital of Philadelphia; Philadelphia (Philadelphia County); On-site; USD 60,317,000 - 75,504,000; Full time

Job summary

Children's Hospital of Philadelphia (CHOP) is seeking a Hands-on Clinical Research Support role under PI supervision. The position involves scheduling participants, data collection and entry, regulatory submissions, and essential documentation across studies.

Candidates should have an HS diploma (Bachelor's preferred) and at least one year of clinical research experience. The role emphasizes HIPAA compliance and adherence to protocols.

Qualifications

• High School Diploma or GED required.
• Bachelor's degree preferred.
• Previous clinical research experience required.
• At least 1 year of relevant clinical research experience preferred.

Responsibilities

• Provide technical and administrative support in the conduct of clinical research.
• Schedule patient/research participant visits and screen for inclusion/exclusion criteria.
• Assist data collection, entry, management, and regulatory submissions.
• Process laboratory samples and support study procedures and documentation.
• Maintain study source documents and ensure IRB/HIPAA compliance.

Skills

IRB knowledge

Education

High School Diploma / GED

Bachelor's Degree preferred

Job description

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

Under the direct supervision of the Principal Investigator and/or other study team members, this role provides support in the conduct of clinical research. Job responsibilities may include human subject research activities including but not limited to subject enrollment, data/sample collection, data entry, and regulatory submissions support.

What you will do

• Provide technical and administrative support in the conduct of clinical research:
• Patient/research participant scheduling
• Patient/Research Participant screening for inclusion/exclusion criteria or case history
• Data collection
• Data entry
• Data management
• Laboratory sample processing
• Clinical research study procedures or questionnaire administration
• Organization of research records and/or other study related documentation
• Research Study Compliance
• Adhere to IRB approved protocols and compliance with HIPAA and handling confidential materials
• Comply with Institutional policies, SOPs and guidelines
• Comply with federal, state, and sponsor policies
• Additional Responsibilities may include:
• Consent subjects, with appropriate authorization and training
• Document and report adverse events
• Maintain study source documents
• Complete case report forms (paper and electronic data capture)
• Assist with IRB/regulatory submissions
• Complete case report forms or other study documentation (paper and electronic data capture)
• Follow-up care
• Order materials/supplies
• Schedule research meetings

Education Qualifications

• High School Diploma / GED Required
• Bachelor's Degree Preferred

Experience Qualifications

• Previous relevant clinical research experience Required
• At least one (1) year of relevant clinical research experience Preferred

Skills and Abilities

• Familiarity with IRB and human subject protection.

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

$21.05 - $26.35 Hourly

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.