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Mitochondrial Myopathy Clinical Research Assistant

1 month ago


Philadelphia, United States The Children’s Hospital of Philadelphia Full time
JOB DESCRIPTION

SHIFT:

Day (United States of America)

We are seeking a motivated individual to join our Mitochondrial Myopathy Research Group in the Children's Hospital of Philadelphia Mitochondrial Medicine Frontier Program (MMFP) in the Division of Human Genetics. 
The Mitochondrial Myopathy Research program focuses on clinical research efforts to develop and validate new outcome measures in Mitochondrial Myopathy for natural history studies and clinical trials as well as to establish new diagnostic approaches and validation of novel methods to measure mitochondrial function.
 
This full-time Clinical Research Assistant role is focused on Clinical Research and Translational research studies including quantitation of physiologic responses to passive exercise therapy. 

Responsibilities would include RedCap data entries from all clinic visits, organization of baseline and longitudinal data, preparing data for the statistician, coordination of collaborator meetings and update presentations, extensive literature review, assist to prepare presentation slides, conference abstracts and manuscripts, and participate in statistical analysis under the guidance and oversight of the statistician. The individual would be working directly with the PI, Dr. Zolkipli-Cunningham and the multidisciplinary Clinical Research team.
 

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 diverse talent who can help us deliver on our mission to be a world leader in the advancement of healthcare for children.

We strongly encourage all candidates of diverse backgrounds and lived experiences to apply.

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 be fully vaccinated against COVID-19 and receive an annual influenza vaccine.

Employees may request exemptions for valid religious and medical reasons. Start dates may be delayed until candidates are immunized or exemption requests are reviewed.

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