The Department of Neurology is seeking a Research Assistant, Safety that will support the BIOS Clinical Trial Coordinating Center (CTCC), which manages multi-center, 20+ million dollar federally funded clinical trials and multiple site-specific pharmaceutical sponsored trials.

Specific Duties & Responsibilities

Safety and Risk Assessment, Surveillance, and Management

• Monitor, document, and resolve safety events for multiple multi-center studies

• Update data and safety monitoring plans in accordance with study modifications

• Develop and document internal safety monitoring processes

• Develop and coordinate clinical event committee tasks, meetings, and regulatory documentation

• Organize and facilitate multi-disciplinary Risk Assessment meetings / Risk Management meetings

• Facilitate Safety Monitoring Plan draft development and version management per funded project

• Facilitate QA Monitoring Plan draft development and version management per funded project

• FDA file management as needed for projects managed by BIOS CTCC

• Manage BIOS CTCC SOP/WI/Form library and training documentation for all Operational plans, FDA submission documents, workflow supporting materials (email templates, CAPA plans, etc.),

• Data management of RACT REDCap, QA effort tracking and various EDC system navigation, Safety Event workflow tracking and various EDC system navigation, FDA system use and submission tracking, financial management to pay MM contractors

• Report to weekly team meeting (per team), weekly trial operations meetings (per trial supported), BIOS Monthly Ops (monthly), manuscript preparation (ad hoc)

Research Support

• Assist with annual reports, IRB applications, and FDA reporting.

• Handle source documents, literature searches, write summaries, assist with writing grants and standard operational procedures, and prepare journal manuscripts.

• Provide analytical support to data analysts and research support as required to include PowerPoint presentations and general correspondence.

• Participate in project related meetings and develop-implement needed quality control procedures and tasks. Organize materials and maintain filing systems.

• Provide telephone and correspondence management.

• Perform data entry and data editing.

• Assist with basic data management tasks such as running queries on existing databases, organizing, and editing data, conducting reliability checks.

• Comply with all regulatory and institutional requirements related to clinical research.

• Combine, distribute, and ship documents.

• Perform other duties as required.

Minimum Qualifications

• Bachelor's Degree in related discipline.

• Additional related experience may substitute for required education, to the extent permitted by the JHU equivalency formula.

Classified Title: Research Assistant

Job Posting Title (Working Title): Research Assistant, Safety

Role/Level/Range: ACRO40/E/03/CD

Starting Salary Range: $17.20 - $30.30 HRLY (Commensurate with experience)

Employee group: Full Time

Schedule: M-F 8:30 am - 5:00 pm

Exempt Status: Non-Exempt

Location: Hybrid/School of Medicine Campus

Department name: SOM Neuro BIOS

Personnel area: School of Medicine

The listed salary range represents the minimum and maximum Johns Hopkins University offers for this position, based on a good faith estimate at the time of posting. Actual compensation will vary depending on factors such as location, skills, experience, market conditions, education, and internal equity. Not all candidates will qualify for the highest salary in the range.

Johns Hopkins provides a comprehensive benefits package supporting health, career, and retirement. Learn more: https://hr.jhu.edu/benefits-worklife/.

Equal Opportunity Employer

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

EEO is the Law

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