Senior Clinical Research Coord: Lead Multi-Site Trials

Washington University in St. Louis; St. Louis (MO); On-site; USD 64,300 - 99,700; Full time

Job summary

Washington University in St. Louis in St. Louis, MO, is seeking a Senior Clinical Research Coordinator to oversee complex, multi-site studies under the Cruchaga lab.

You will coordinate regulatory compliance, supervise coordinators, and ensure smooth clinical operations. You will liaise with the PI, manage study startup, data collection, and site visits, and assist in drafting manuscripts and grant proposals.

Qualifications

• Bachelor's degree or equivalent education/experience may substitute for minimum education.
• Basic Life Support certification is required per the posting.
• Clinical Research experience of 3 years is noted.

Responsibilities

• Acts as the primary liaison to PI in developing plans for clinical research projects; collaborates in manuscript preparation and grant proposals.
• Evaluates and interprets collected data; prepares presentations and reports with progress trends.
• Manages study startup, launch, and regulatory document maintenance; ensures regulatory compliance; coordinates with funding agencies.
• Develops forms, questionnaires, and manuals; assists in budget review and invoicing.
• Trains and supervises research staff; participates in hiring and evaluations.
• Facilitates site visits by monitors and auditors.
• Oversees data collection and specimen handling; coordinates study/project management tasks.

Skills

Clinical Research Management

Clinical Study Protocols

Computer Systems

Database Management

Data Entry

Detail-Oriented

Freezerworks (Software)

Interpersonal Communication

Microsoft Office

Ordering Supplies

Organizing

Participant Recruiting

Research Projects

Research Support

Written Communication

Education

Bachelor's degree or equivalent

Tools

Freezerworks (Software)

Job description

Washington University in St. Louis in St. Louis, MO, is seeking a Senior Clinical Research Coordinator to oversee complex, multi-site studies under the Cruchaga lab.

You will coordinate regulatory compliance, supervise coordinators, and ensure smooth clinical operations. You will liaise with the PI, manage study startup, data collection, and site visits, and assist in drafting manuscripts and grant proposals.