Clinical Research Assistant II (Behavioral Pharmacology Research Unit)

Johns Hopkins University•Baltimore, MD

1d•Onsite

About The Position

The Behavioral Pharmacology Research Unit is seeking a Clinical Research Assistant II who reports to the Sr. Clinical Research Manager. Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. The Clinical Research Assistant II will support the research team by implementing steps and processes of a clinical research protocol. The position will perform both administrative tasks related to day-to-day clinical research operations, and protocol-related duties requiring an understanding of research procedures.

Requirements

High school diploma or graduation equivalent.
One year of related experience.
Additional education may substitute for required experience and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.

Nice To Haves

Bachelor's Degree in a related field.
Administrative Skills - Awareness
Clinical Research - Awareness
Clinical Research Knowledge - Awareness
Data Entry - Awareness
Data Collection and Reporting - Awareness
Data Management and Analysis - Awareness
Information Gathering - Awareness
Interpersonal Skills - Awareness
Organizational Skills - Awareness

Responsibilities

Collect study data by recruiting and coordinating activities of study participants.
Utilize a basic understanding of the clinical study background and rationale to explain the study to potential and current participants.
Assist in developing recruitment strategies for one or more studies.
Implement a variety of techniques for recruitment, e.g., print and web based advertisements, contact referring physicians, participate in community events, etc.
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 related to study accrual, study trends, efficiency-related issues.
Contact participants to confirm, schedule, and retain.
Perform data entry, edit, and verify data collected in test sessions to ensure accuracy.
Maintain current backups of research data and ensure the security and confidentiality of all study data.
Organize data in approved systems and maintain study logs across multiple platforms and study phases.
Administer questionnaires and clinical assessments under the direction of senior research staff.
Collect, process, and handle urine specimens; support post-draw biospecimen handling, storage, and shipping preparation.
Other duties as assigned.