Neurodegenerative Clinical Research Coordinator II

Washington University in St. Louis; St. Louis (MO); On-site; USD 55,000 - 82,000; Full time

Benefits offered by this job

Vacation & holidays

Health insurance

Transit fare benefits

Tuition assistance

Job summary

Washington University in St. Louis seeks a coordinator in the THuNDR Laboratory for postmortem brain research and coordination across AD and movement disorder studies.

You will liaise with school leadership, PIs, and research sites to ensure protocol compliance and smooth study operation. Responsibilities include developing plans, writing manuals, coordinating forms, reviewing literature, coordinating data collection, and preparing progress reports and manuscripts; this is a non-clinical

Qualifications

• Bachelor’s degree or combination of education and/ or experience may substitute for minimum education.
• 2 years of clinical research experience.
• Basic Life Support (BLS) certification.

Responsibilities

• Assist develop plans for research projects and interpret results; collaborate on manuscripts and grant proposals.
• Coordinate forms, questionnaires, and data collection; write manuals for study progress and coding.
• Implement all phases of study; ensure protocol compliance and regulatory requirements.
• Evaluate clinical data; prepare reports and summaries with progress insights.
• Perform other duties as assigned.

Skills

Clinical Research

Clinical Study Protocols

Communication

Interpersonal Communication

Interpersonal Dynamics

Interpersonal Interactions

Interpersonal Relationships

Research Projects

Spreadsheet Analysis

Education

Bachelor’s degree

Basic Life Support (BLS)

Clinical Research – 2 years

Job description

Washington University in St. Louis seeks a coordinator in the THuNDR Laboratory for postmortem brain research and coordination across AD and movement disorder studies.

You will liaise with school leadership, PIs, and research sites to ensure protocol compliance and smooth study operation. Responsibilities include developing plans, writing manuals, coordinating forms, reviewing literature, coordinating data collection, and preparing progress reports and manuscripts; this is a non-clinical