Clinical Research Assistant Eating DisorderResearch Program - Part time

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A Brief Overview

The Timko Research Group (see https://www.med.upenn.edu/timkolab/) in the Eating DisorderResearch Program at Children's Hospital of Philadelphia (CHOP) is seeking a research assistant forstudies focused on adolescents with eating disorders, with a particular focus on anorexia nervosa.

The RA will be responsible for recruitment, enrollment, assessment, and follow up for adolescentsand their parents who are enrolled in various studies. The RA will be responsible for

1) Assistingin the day-to-day administration of research projects

2) Maintaining subject tracking system andscheduling subjects for assessments

3) Creating reports regarding enrollment rates

4) Creating and maintaining the study database

5) Conducting follow-up interviews with families and
medical providers

6) Data abstraction from the electronic medical record.

Importantly, the RA must be able to move betweenCHOP sites, including multiple locations within the city of Philadelphia and the Middleman FamilyPavilion in King of Prussia.

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.

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SALARY RANGE:

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.