Plastic Surgery Research Coordinator (Clinical Trials)

Opportunity for Health; Philadelphia (Philadelphia County); Hybrid; USD 45,000 - 48,000; Full time

Benefits offered by this job

Health insurance

Tuition benefits

Retirement plans

Time Off (vacation/sick leave)

Job summary

The Division of Plastic Surgery at the University of Pennsylvania invites applications for the Research Scholar position. This role offers an opportunity for current medical students or medical residents to work closely with the Division of Plastic Surgery as a member of a research team.

The position focuses on organizing and managing research projects, gaining experience in study design, IRB submissions, data management, and conducting retrospective and prospective clinical trials under senior

Qualifications

• Bachelor's degree and 1 to 2 years of experience or equivalent combination of education and experience is required.
• Current medical/surgical resident or current medical student who at minimum completed first year of medical school.
• Two letters of recommendation and a personal statement for the application process. This position is contingent upon grant funding.

Responsibilities

• Organize, gain approval, and manage the majority of the research produced within the division under direction from senior clinical research staff.
• Develop skills in planning, implementation, and conducting retrospective and prospective clinical trials and in managing and analyzing institutional and national datasets.
• Prepare abstracts for scientific meetings and manuscripts for publication; assist in divisional quarterly research meetings and conference posters/presentations.

Education

Bachelor's degree

Job description

The Division of Plastic Surgery at the University of Pennsylvania invites applications for the Research Scholar position. This role offers an opportunity for current medical students or medical residents to work closely with the Division of Plastic Surgery as a member of a research team.

The position focuses on organizing and managing research projects, gaining experience in study design, IRB submissions, data management, and conducting retrospective and prospective clinical trials under senior