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General Information

Work Location: Los Angeles, USA
Onsite or Remote
Fully On-Site
Work Schedule
Monday-Friday, 8am-5pm
Posted Date
07/19/2024
Salary Range: $33.63 - 54.11 Hourly
Employment Type
2 - Staff: Career
Duration
Indefinite
Job #
18061

Primary Duties and Responsibilities

Join our dynamic team as a Clinical Research Coordinator, where you will play a vital role in managing clinical research projects from inception to completion.

In this key position, you will:

  • Lead and Manage Studies: Oversee the design, setup, conduct, and closeout of one or more clinical studies, ensuring every phase aligns with study objectives and regulations.
  • Coordinate Research Activities: Implement and manage research activities, ensuring projects stay on track and meet deadlines efficiently.
  • Ensure Compliance: Plan and organize tasks to adhere to study protocols and regulations, including institutional policies, FDA CFR, and ICH GCP guidelines.
  • Collaborate Effectively: Collaborate with Principal Investigators, ancillary departments, research infrastructure teams, sponsors, and other stakeholders to support all aspects of study administration. 

Your responsibilities will also include ensuring compliant conduct, managing financial aspects, and providing adequate personnel support for the studies.

Salary: $33.63 - $54.11 hourly


Job Qualifications

Required: 

  • Bachelors Degree or 1-3 years of previous study coordination or equivalent clinical research coordination experience/training. 
  • Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborative relationships.
  • Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.
  • Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.
  • Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.
  • Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.
  • Ability to handle confidential material information with judgement and discretion.
  • Working knowledge of the clinical research regulatory framework and institutional requirements.
  • Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
  • Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.

As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.