Clinical Research Assistant II — Study Coordination & Data

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

Job summary

The Johns Hopkins University in Baltimore, MD, seeks a Clinical Research Assistant II to support the Behavioral Pharmacology Research Unit. The role includes administrative duties and protocol-specific tasks under the supervision of the Sr. Clinical Research Manager.

Responsibilities cover recruitment, data collection, IRB coordination, and routine reporting. A strong attention to detail, organizational skills, and privacy compliance are essential.

Qualifications

• High school diploma or graduation equivalent.
• One year of related experience.
• Additional education may substitute for required experience to the extent permitted by the JHU equivalency formula.
• Preferred: Bachelor's Degree in a related field.

Responsibilities

• Recruit and coordinate activities of study participants.
• Explain the study background to potential and current participants.
• Assist in developing recruitment strategies for one or more studies.
• Implement recruitment techniques (print/web ads, referrals, community 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 administrative matters.
• Prepare routine reports on accrual, trends, and efficiency issues.
• Contact participants to confirm, schedule, and retain participants.
• Other duties as assigned.

Skills

Administrative Skills - Awareness

Clinical Research Knowledge -Awareness

Data Entry - Awareness

Data Collection and Reporting -Awaren

Interpersonal Skills - Awareness

Organizational Skills - Awareness

Education

High school diploma or GED

Bachelor's Degree in a related field

Job description

The Johns Hopkins University in Baltimore, MD, seeks a Clinical Research Assistant II to support the Behavioral Pharmacology Research Unit. The role includes administrative duties and protocol-specific tasks under the supervision of the Sr. Clinical Research Manager.

Responsibilities cover recruitment, data collection, IRB coordination, and routine reporting. A strong attention to detail, organizational skills, and privacy compliance are essential.