Clinical Research Coordinator II: Bone Marrow & Leukemia Trials

Washington University; United States; On-site; USD 55,000 - 82,000; Full time

Benefits offered by this job

Vacation days

Holiday leave

Sick time

Health insurance

Metro U‑Pass

Retirement plan

Tuition assistance

Caregiver leave

Job summary

Washington University in St. Louis seeks a research study coordinator to assist investigators on a complex clinical trial in St. Louis, MO. You will liaise with the school, sponsor, community and participants, and manage all phases of the protocol to ensure compliance.

This role requires a bachelor’s degree and 2 years of clinical research experience, plus BLS certification. You will develop forms, monitor adverse events, and prepare reports while upholding regulatory standards.

Qualifications

• Bachelor’s degree or combination of education and experience may substitute for minimum education.
• Basic Life Support certification (AHA and Red Cross).
• Minimum 2 years of clinical research experience.
• Driver’s license not required.
• Strong record-keeping and regulatory compliance.

Responsibilities

• Assists in developing plans for research projects and discusses the interpretation of results.
• Collaborates in manuscript preparation and grant proposals to sponsors.
• Coordinates amendments to protocols and study design as appropriate.
• Develops forms, questionnaires and data collection procedures.
• Writes instructional manuals for study progress, data collection and coding.
• Monitors adverse events and participant progress with regulatory oversight.
• Ensures protocol compliance and communicates with funding agencies.
• Prepares progress reports and presentations with data analyses.

Skills

Clinical research

Clinical study protocols

Database management

Spreadsheet analysis

SAS

Education

Bachelor’s degree

Job description

Washington University in St. Louis seeks a research study coordinator to assist investigators on a complex clinical trial in St. Louis, MO. You will liaise with the school, sponsor, community and participants, and manage all phases of the protocol to ensure compliance.

This role requires a bachelor’s degree and 2 years of clinical research experience, plus BLS certification. You will develop forms, monitor adverse events, and prepare reports while upholding regulatory standards.