Description

The Semel Institute is seeking to hire a part-time Assistant Clinical Research Coordinator who will contribute to the overall operational management of research/study activities from design, set up, conduct, through closeout. 

 

In this position you will be responsible for:

 

Coordination of research activities for one or more studies.  Recognizing and performing necessary tasks to coordinate projects and prioritizes work to meet necessary deadlines.  Participating in planning and organizing necessary tasks to ensure adherence to the study protocol an applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP).  Collaborating with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. 

The responsibilities outlined in the job description provide a general overview of duties and tasks performed by Clinical Research Coordinators. Performance of duties and tasks will vary based on the department operations, the type of study and scope of service.

 

Pay Range: $27.08 – $43.55 hourly