Clinical Research Associate- Magnetic Resonance Spectroscopy

Children’s Hospital of Philadelphia•Philadelphia, PA

About The Position

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 This role performs clinical research activities with a focus on technical and analytical work in support of the data analysis and data management needs of the team. Gathering, analyzing, and making recommendations or decisions based on data is key as it relates to manuscript writing and reporting to different federal agencies. May have minimal patient-facing coordination responsibilities. The Saleh Lab at the Children’s Hospital of Philadelphia (CHOP) has a Clinical Research Associate opening for individuals who are interested in building novel magnetic resonance spectroscopy sequences and reconstruction. The project(s) will use these novel methods to enhance understanding of diseases and progression in individuals with brain diseases. This CRA position will broaden your skillset, scientific background, and research capabilities. Successful applicants will be highly self-motivated, detail-focused, flexible, and fast learners who enjoy working in bustling research and clinical environments. This research is overseen by Dr. Muhammad Saleh (principal investigator) and Dr. Timothy Roberts. As a Program in Advanced Imaging Research (PAIR) member at CHOP, the individual can participate in outreach events and attend lectures and seminars on various diseases and development research, allowing exposure to scientific and clinical leaders in the field.

Requirements

Bachelor's Degree - Required
At least one (1) year quantitative analysis, data management or regulatory research experience - Required
Advanced knowledge of medical terminology
Intermediate knowledge of clinical research methods
Intermediate knowledge of international regulations regarding research, Good Clinical Practices (ICH / GCP)
Intermediate knowledge of HIPPA regulations and policies and procedures governing human subjects research
Basic knowledge of Institutional Review Board (IRB) processes and policies
Basic knowledge of research design, data analysis and writing
Intermediate proficiency with electronic medical record software (EPIC)
Intermediate proficiency with office software (Microsoft Office) including word processing, spreadsheet, and presentation software (Word, Excel, PowerPoint)
Basic proficiency with academic / reference management applications (EndNote, Mendeley)
Basic proficiency with electronic data management systems (REDcap)
Familiarity with survey software (Qualtrics), online crowdsourcing marketplaces (MTurk) and statistical software (SPSS/SAS) R/Python
Excellent verbal and written communications skills
Excellent critical thinking / problem-solving skills

Nice To Haves

Master's Degree in a related field - Preferred
At least three (3) years quantitative analysis, data management or regulatory research experience - Preferred
At least three (3) years of relevant and complex clinical research experience - Preferred

Responsibilities

Plan and direct activities, methods, and treatments.
Collaborate internally to review, improve and promote processes and procedures.
Manage related data collection, analysis, management and databases / system use.
Ensure activity compliance and quality control with protocol and regulatory requirements.
Coordinate compliance, documentation and submissions for regulatory agencies.
Direct and maintain related documentation, records, and events.
Assist with activities including assessments, enrollment and collection.
Assist with researching to develop methodologies, instrumentation and procedures.
Participate in department presentations and publications.
Supporting Investigators in grant preparation (draft methods, contribute to strategy component)
Presentations, Publications, and related development
Assists in reporting (progress) and methods for applications
Patient coordination