Senior Clinical Research Coordinator — Study Oversight

Washington University in St. Louis; Ann Arbor (MI); Sur place; USD 36 000 - 54 000; Plein temps

Avantages offerts par ce poste

Vacation time

Health insurance

Transit benefit

Tuition assistance

Résumé du poste

Washington University in St. Louis in Saint Louis, MO, seeks a Clinical Research Coordinator to assist investigators on a complex study, potentially handling multiple studies at once.

You will liaise with the school, sponsoring agency, community, and participants, ensuring compliance with the study protocol. The role involves plans for research projects, development of forms and manuals, data collection and coding, regulatory oversight, and analysis of clinical data.

Qualifications

• Education: Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• Certifications / Professional Licenses: Basic Life Support (BLS) from American Heart Association or Red Cross.
• Work Experience: Clinical Research (2 Years).
• Skills: Not applicable to list here.

Responsabilités

• Assists in developing plans for research projects and discusses interpretation of results; helps prepare manuscripts and grant proposals.
• Coordinates development of forms, questionnaires, and procedures; writes instructional manuals for study progress and data collection.
• Implements and manages all phases of study/protocol; ensures regulatory compliance; maintains records; monitors participant progress; reports adverse events; liaises with funding agencies.

Connaissances

Clinical Research

Clinical Study Protocols

Database Management

Research Projects

Spreadsheet Analysis

SAS

Formation

Bachelor’s degree or combination of education and/or experience

Outils

Basic Life Support

Description du poste

Washington University in St. Louis in Saint Louis, MO, seeks a Clinical Research Coordinator to assist investigators on a complex study, potentially handling multiple studies at once.

You will liaise with the school, sponsoring agency, community, and participants, ensuring compliance with the study protocol. The role involves plans for research projects, development of forms and manuals, data collection and coding, regulatory oversight, and analysis of clinical data.