Clinical Research Coordinator — Multisite Trials Lead

University of Pennsylvania Perelman School of Medicine; Kirkkonummi; On-site; EUR 42,000 - 48,000; Full time

Job summary

University of Pennsylvania Perelman School of Medicine in Philadelphia, PA is seeking a Clinical Research Coordinator A/B to manage and monitor multi-site clinical trials within the Department of Surgery. You will coordinate subject recruitment, data entry, IRB submissions, and ensure compliance with protocols and regulatory requirements.

The role supports study teams, mentors coordinators, and collaborates with partner institutions to develop budgets and manage study expenses, with emphasis on

Qualifications

• Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required. (CRC-A)
• Bachelor of Science and 2 to 3 years of experience or equivalent combination of education and experience is required. (CRC-B)

Responsibilities

• Coordinate and conduct clinical studies, including subject recruitment, informed consent, chart maintenance and data entry.
• Coordinate IRB submissions and renewals in accordance with FDA and IRB guidelines.
• Assure compliance with the protocol and regulatory requirements including data capture and source documentation.
• Oversee study preparation and blood sample processing and analysis.
• Database management and analysis.
• Ordering and stocking supplies, maintaining equipment.
• Educate patients and family members.
• Promote good clinical practice and knowledge of regulations in human subject protection.
• Other duties and responsibilities as assigned.

Education

Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience (CRC-A)

Bachelor of Science and 2 to 3 years of experience or equivalent combination of education and experience (CRC-B)

Job description

University of Pennsylvania Perelman School of Medicine in Philadelphia, PA is seeking a Clinical Research Coordinator A/B to manage and monitor multi-site clinical trials within the Department of Surgery. You will coordinate subject recruitment, data entry, IRB submissions, and ensure compliance with protocols and regulatory requirements.

The role supports study teams, mentors coordinators, and collaborates with partner institutions to develop budgets and manage study expenses, with emphasis on