Research Associate - Administrative
Compu-Vision Consulting Inc. | Santa Monica | www.resume-library.com |
Clinical Research Coordinator
Location: 1000 Veteran Ave 32-59, Los Angeles, CA 90095
Duration: 26 week contract
Shift: Monday through Friday, 8:00 am to 5:00 pm
REQUIRED EXP: At least 1-2 years of study coordinator experience. Must have experience with PI initiated studies, including study setup, source documentation, etc. PREFERRED: ACRP cert
Job duties include:
The Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The position has responsibility for the implementation of research activities for one or more studies.
The incumbent recognizes and performs necessary tasks to manage projects and prioritizes work to meet necessary deadlines. The incumbent is responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP).
The Clinical Research Coordinator collaborates 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.
Required Experience:
At least 1-2 years of study coordinator experience
Must have experience with Principal Investigator initiated studies, including study setup, source documentation, etc.
Location: 1000 Veteran Ave 32-59, Los Angeles, CA 90095
Duration: 26 week contract
Shift: Monday through Friday, 8:00 am to 5:00 pm
REQUIRED EXP: At least 1-2 years of study coordinator experience. Must have experience with PI initiated studies, including study setup, source documentation, etc. PREFERRED: ACRP cert
Job duties include:
The Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The position has responsibility for the implementation of research activities for one or more studies.
The incumbent recognizes and performs necessary tasks to manage projects and prioritizes work to meet necessary deadlines. The incumbent is responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP).
The Clinical Research Coordinator collaborates 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.
Required Experience:
At least 1-2 years of study coordinator experience
Must have experience with Principal Investigator initiated studies, including study setup, source documentation, etc.
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