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Assoc Analyst, Device Management

Date Posted: 7/11/2019

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Job Description

A large, global medical device company in Irvine has an opportunity for an Associate Analyst, for Device Managememt.  Will Identify, develop, recommend, and implement basic process development and process improvement solutions to trial workflow timelines (e.g., device accountability data) with guidance from management Analyze site data of device accountability Collaborate with stakeholders (e.g., Finance, Customer Service) on variance discrepancies between site and JDE data Regular communicate with site to resolve basic queries Provide training on electronic database for cross functional team members (e.g., clinical specialist and field monitors) Partner with Quality to resolve device related issues Work is performed independently on sections of projects and/or lines of work and reviewed for accuracy and soundness Participates in arranging own activities in accomplishing objectives Contributes to the completion of sections of organizational projects and goals Errors in judgment or failure to achieve results may require some expenditures of resources to rectify Develops solutions to a variety of problems of basic scope and complexity Participates in basic process improvements

We are an equal opportunity employer and make hiring decisions based on merit. Recruitment, hiring, training, and job assignments are made without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, or any other protected classification. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Job Requirements

Skills:
• Good understanding and knowledge of fundamental principles, theories, and concepts relevant to clinical trial management
• Good understanding and knowledge of clinical device accountability
• Good problem-solving, organizational, analytical and critical thinking skills
• Ability to manage confidential information with discretion
• Good knowledge of regulatory requirements (e.g., CFR, GCP) and documents
• Good knowledge in Microsoft Office Suite, including Excel, JDE, electronic database (e.g., Salesforce) required
• Good written and verbal communications skills
• Good problem-solving skills
• Ability to manage confidential information with discretion
• Strict attention to detail
• Ability to interact professionally with all organizational levels
• Ability to manage competing priorities in a fast-paced environment
• Must be able to work in a team environment, including immediate supervisor and other team members in the section or group
• Ability to build productive internal/external working relationships

Education & Experience
• Bachelor’s degree in related field required
• 1 year of previous clinical trial management experience required
Posted By: tlebeau@ultimatestaffing.com

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Job Snapshot

  • Employee Type:Full-Time
  • Location:Irvine, CA
  • Job Type:Science
  • Experience:Not Specified
  • Education:Not Specified
  • Date Posted:7/11/2019
  • Contact: Teresa LeBeau (949) 250-3511
  • Pay Range: $0.00 - $0.00 Annually
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Job Reference: JO-1907-64267