Senior Clinical Research Coordinator - Hematology/Oncology (Santa Barbara)
Santa Barbara, CAFull-time
Behavioral Health Market Context
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Job Description
nical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities. Recognize and perform necessary project management tasks and prioritizes work to reach scheduled goals. The Senior Clinical Research Coordinator is a technical leader responsible for ensuring the study protocol and procedures have been completed accurately, safely, and in a timely manner. This position may supervise and train others on projects as necessary. Work with PIs, departments, sponsors, institutions, and other entities as needed to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of studies.
The full annual salary range for this position is: $89,454.77 - $143,904.50
The full annual salary range for this position is: $89,454.77 - $143,904.50
Qualifications
Benefits
- •The full annual salary range for this position is: $89,454.77 - $143,904.50
Responsibilities
- •The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout
- •The ideal candidate is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities
- •Recognize and perform necessary project management tasks and prioritizes work to reach scheduled goals
- •The Senior Clinical Research Coordinator is a technical leader responsible for ensuring the study protocol and procedures have been completed accurately, safely, and in a timely manner
- •This position may supervise and train others on projects as necessary
- •Work with PIs, departments, sponsors, institutions, and other entities as needed to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of studies
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