Clinical Research Specialist

2 months ago


Irvine, United States Kelly Science, Engineering, Technology & Telecom Full time

Join Kelly FSP as a Clinical Research Specialist with our Medical Device client in Irvine, CA

This is a hybrid position Tuesday/Thursday and every other Friday on site.



RESPONSIBILITIES


Serves as a Clinical Research Specialist within the Clinical R&D Operations CoE operations group to execute company sponsored clinical trials for the Medical Device Franchises

Serves as a member of the clinical trial/study core team and may serve as the liaison with the Clinical R&D Franchise and Clinical R&D BSDM for projects under his/her responsibility

May serve as the primary contact for clinical trial sites

Manage operational activities of assigned clinical studies within the Clinical R&D Operations group

Solves problems with support from Clinical Management arising during clinical trial execution

Provide internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders

May be involved in other tasks to support Clinical R&D Operations and R&D Clinical Franchise as needed

Track assigned projects budgets to ensure adherence to business plans

Support the implementation of new clinical systems/processes, and provide support for publications, as needed.

Interface and collaborate with site personnel, IRBs/ECs, Competent Authorities/MoH, contractors/vendors, and company personnel

Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance

Ensure efficient use of resources within the clinical study/program to provide high quality deliverables.


Business Leadership Responsibilities:

Accountable for quality, compliance with regulations and company procedures, timelines, and budgets for assigned clinical trials.

May lead several non-regulated small clinical trials and/or a small number of non-regulated medium trials that may involve other clinical operations staff (i.e.,



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