Clinical Research Project Manager A

Job Description Summary

The Project Manager A will organize, coordinate and implement multiple clinical trials under the guidance of senior staff. They will maintain and oversee all aspects of regulatory. They will oversee the creation of source documents and ensure that all data is of high quality and meets all regulations. They will serve as a liaison between investigators, external collaborators and internal staff, meeting regularly. They will be responsible for training new staff.

Job Responsibilities

• Managing day-to-day study activities, including subject recruitment, screening, enrollment, and conducting study visits.
• Preparing and maintaining essential study documentation such as protocols, informed consent forms, and IRB submissions to ensure adherence to federal and institutional guidelines.
• Overseeing the construction of databases and case report forms (CRFs), as well as performing data entry, cleaning, and quality control for interim analyses.
• Serving as a primary liaison between investigators, internal study teams, and external collaborators to track project milestones and timelines.
• While typically working under moderate supervision, they may provide limited guidance/training orientation or task coordination to research coordinator.

Position Contingent Upon Funding

Qualifications

Bachelor's Degree with 3-5 years of related experience or equivalent combination of education and experience is required.

Preferred:

• Experience assisting with study start-up activities (e.g., preparing protocols, consent forms, and SOPs).
• Familiarity with IRB submissions and human subjects' protection regulations.
• Proficiency in data tools like REDCap and Excel.
• Strong organizational and communication skills for coordinating with internal teams and external collaborators.
• Master's Degree

Job Location - City, State

Philadelphia, Pennsylvania

Department / School

Perelman School of Medicine