Remote Clinical Trials Research Program Assistant II

The Johns Hopkins University; Baltimore (MD); On-site; USD 22,000 - 37,000; Part time

Job summary

The Johns Hopkins University in Remote location is seeking a Research Program Assistant II to support clinical trials and studies. You will assist with recruitment, data collection, and administration of the protocol, ensuring data quality and compliance.

Responsibilities include coordinating participant activities, maintaining study documents, and communicating with the research team and IRB. The role requires strong organizational and analytical abilities and attention to detail.

Qualifications

• High school diploma or GED required.
• At least one year of related experience.
• Education may substitute for experience and vice versa as permitted by JHU policy.

Responsibilities

• Collect study data by recruiting and coordinating activities of study participants.
• Explain the study background and rationale to participants.
• Assist in developing recruitment strategy for one or more studies.
• Implement recruitment techniques (ads, physicians, events).
• Set up tools and procedures for data collection and study processes.
• Perform data entry and organize data in approved systems.
• Serve as liaison between study team and IRB for routine admin matters.
• Prepare routine reports related to accrual, trends, and efficiency.
• Contact participants to confirm, schedule, and retain participants.
• Other duties as assigned.

Skills

Administrative skills

Clinical research

Data entry

Data collection & reporting

Data management & analysis

Organizational skills

Interpersonal skills

Communication skills

Attention to detail

Education

High school diploma or GED

One year related experience

Bachelor’s degree in a related field

Tools

MS Word

Excel

PowerPoint

Job description

The Johns Hopkins University in Remote location is seeking a Research Program Assistant II to support clinical trials and studies. You will assist with recruitment, data collection, and administration of the protocol, ensuring data quality and compliance.

Responsibilities include coordinating participant activities, maintaining study documents, and communicating with the research team and IRB. The role requires strong organizational and analytical abilities and attention to detail.