Clinical Research Coordinator - part time in Eye

This part‑time Study Coordinator, working closely with the Principal Investigator (PI) and other study investigators, is funded by PEDIG. The study is named “Myopia Treatment Study 2 (MTS2)”. This individual will coordinate research through project recruitment, scheduling and retention of study subjects, and exercise appropriate communication skills when acting as a liaison between the Drexel site, the lead site, and study participants. This individual will conduct data entry, submit materials to the Institutional Review Board, maintain study records, and execute certain administrative tasks. While this is a hybrid role, the majority of on‑site work will occur at The Eye Institute and occasional visits to the Drexel University, Elkins Park Campus and Drexel University, University City Campus will be required. Additionally, there will be online study group meetings monthly. The Coordinator will be assisting with this study and other studies as needed.

Essential Functions

• Assist in identifying, recruiting, and obtaining informed consent from eligible participants for research study.
• Ensure coordination of subjects and study personnel as required by protocol and Good Clinical Practice (GCP) guidelines.
• Act as liaison between the Drexel Institutional Review Board and external site Institutional Review Boards while utilizing the SMART IRB Reliance System.
• Encourage and motivate participants to maintain compliance and attendance throughout the study and coordinate all retention aspects.
• Maintain study records and related documentation as required by protocol and regulatory bodies (internal and external).
• Work with external study sites and coordinating centers as required.
• Schedule, participate in, and record minutes for study meetings (in‑person and virtually) as required.
• Maintain the highest level of confidentiality regarding patient and study records.
• Support and complete all study related paperwork including submissions to the Internal Review Board.
• Other related duties as assigned.

Required Qualifications

• Minimum of a Bachelor's Degree in the related field or the equivalent combination of education and work experience.
• Minimum of 3 years in a similar administrative position.
• Experience in clinical trials or other health‑related programs/research preferred.
• Demonstrated experience with research and project coordination.
• Demonstrated experience in research data collection and quality control.
• Experience with data entry, including knowledge of database, word processing, and spreadsheet applications (e.g., REDCap, MS Word, Excel).
• Experience maintaining files and keeping research records.
• Experience preparing and submitting Institutional Review Board documentation such as amendments, continuing reviews, and reportable new information submissions.
• Excellent written, verbal, and interpersonal communication skills, including tact, diplomacy, and flexibility.
• Excellent planning, organizational skills, and ability to work in a changing, multiple demand setting.
• Thorough knowledge of protocol and goals of studies.

Physical Demands

Typically sitting at a desk/table.

Location

The Eye Institute - Oak Lane.

Additional Information

This position is classified as Part Time Non-Exempt, grade J. Compensation for this grade ranges from $22.74 to $34.11 per hour. The offered rate for this position typically aligns with the minimum to midrange of this grade, but it can vary based on the successful candidate’s qualifications and experience, department budget, and an internal equity review. Applicants are encouraged to explore the Professional Staff salary structure and Compensation Guidelines & Policies for more details on Drexel’s compensation framework. For information about benefits, please review Drexel’s Benefits Brochure.