Clinical Research Coordinator - Grant-Funded Ethnography

University of Pennsylvania; Philadelphia (Philadelphia County); Hybride; USD 53 000 - 58 000; Plein temps

Avantages offerts par ce poste

Health benefits

Tuition benefits

Retirement benefits

Professional development

Health and wellness programs

Résumé du poste

The University of Pennsylvania’s Perelman School of Medicine in Philadelphia is seeking a Clinical Research Coordinator B to support day-to-day research and administrative activities across MEHP projects. This full-time role offers a variable hybrid schedule with 2–5 days in person depending on project needs.

Responsibilities include participant recruitment, data management, IRB documentation, and coordination with researchers, clinicians, patients, and staff to advance grant-funded studies

Qualifications

• Bachelor of Science and 2–3 years of experience or equivalent combination of education and experience.
• Knowledge of HIPAA privacy rules and IRB procedures.
• Ability to work across disciplines — medicine, law and medical ethics.
• Experience working with patients and families desired.

Responsabilités

• Recruit participants and manage ongoing communications and payments for participants and collaborators.
• Collect and manage ethnographic data, writings, and interview materials.
• Develop ethnographic processes and interview guides for varied participants.
• Conduct ethnographic observations and qualitative interviews.
• Synthesize observations, communications, and interviews; assist manuscript development.
• Coordinate and oversee IRB study documentation.

Connaissances

HIPAA knowledge

IRB procedures

Interdisciplinary collaboration

Patient interaction

Formation

Bachelor of Science

Description du poste

The University of Pennsylvania’s Perelman School of Medicine in Philadelphia is seeking a Clinical Research Coordinator B to support day-to-day research and administrative activities across MEHP projects. This full-time role offers a variable hybrid schedule with 2–5 days in person depending on project needs.

Responsibilities include participant recruitment, data management, IRB documentation, and coordination with researchers, clinicians, patients, and staff to advance grant-funded studies