Clinical Research Specialist - Contract

TalentBurst, Inc.

Irvine, CA

JOB DETAILS
SALARY
$45–$55 Per Hour
SKILLS
Clinical Data Management, Clinical Practices/Protocols, Clinical Research, Clinical Study Publications, Clinical Trial, Contract Management, Cross-Functional, Documentation, FDA (Food and Drug Administration), GCP (Good Clinical Practices), Process Analysis, Process Development, Process Improvement, Regulations, Regulatory Compliance, Regulatory Requirements, Research Contracts, Standard Operating Procedures (SOP), Startup
LOCATION
Irvine, CA
POSTED
Today

Position: Clinical Research Specialist, Req# 18246-1

This is an in-house CRA Role.
Location: Irvine, CA (100% onsite)
Duration: 12+ monthscontract to hire

 

Job Description:

The main function of a clinical research specialist is to perform study start-up and conduct activities including ICF review that meet regulatory requirements, creating study specific essential document lists, managing and communicating the status of study progress and activities.

 

Education and Experience: 

  • Bachelor's Degree or equivalent in a related field
  • 2-4 years of experience required
  • Clinical background, familiar with clinical study process, monitoring, GCP and clinical study relevant regulations.
  • High compliance requirements and understanding that the rights and well-being of human subjects should be protected during a clinical study

 

Key Responsibilities: 

  • Perform study start-up and conduct activities including ICF review that meets regulatory requirements, creating study specific essential document lists, managing and communicating the status of study progress and activities
  • Identify and investigate discrepancies in study documentation by applying clinical protocol and GCP knowledge and develop processes to mitigate reoccurrence throughout study phases
  • Identify and investigate discrepancies in study documentation by applying clinical protocol and GCP knowledge and develop processes to mitigate reoccurrence throughout study phases
  • Conduct in-house and site (if applicable) reviews of associated documentation and participate in internal and competent authority (e.g., FDA, DEKRA, PMDA) audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Edwards internal SOPs, and US and OUS regulations
  • Assess current processes, identify opportunities and propose solutions to improve process efficiency within and across related functional areas
  • Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution

 #TB_PH
#ZR

About the Company

T

TalentBurst, Inc.

For over 20 years, TalentBurst Inc. has been an award-winning provider of cutting-edge Workforce Management Solutions. With a strong commitment to staying ahead in the tech landscape, we pioneer innovative approaches to talent acquisition. Our expertise spans Life Sciences, and Healthcare Staffing, Banking, Financial, IT, and Engineering, as well as Global Employer of Record (EOR), Agent of Record (AOR), State, Local Government and Education (SLED), and IC validation/compliance services. Additionally, our division, TalentProcure, leads the industry with offerings such as High Hazard Payroll, Managed Services, and Vendor on Premise (VOP) solutions.

Due to our prioritization of excellent standards, we are Joint Commission Certified and are a certified Minority Business Enterprise (MBE) in the USA and Canada. Supporting over 130 Fortune 500 companies globally, we excel in navigating the landscape of talent acquisition. In a world of constant change, we embrace developing people-centric solutions that address the unique demands of our clients. Stay connected by visiting our website and following us on social media!

 

COMPANY SIZE
5,000 to 9,999 employees
INDUSTRY
Staffing/Employment Agencies
FOUNDED
2002
WEBSITE
http://www.talentburst.com/