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Senior Clinical Research Coordinator - Urology

$82.71k - $133.07k

University of California

Job Title

Work Location: Los Angeles, CA, USA

Onsite or Remote Fixed Hybrid Work Schedule Monday-Friday 8am-5pm; hours may vary

Salary Range: $82705.68 - 133068.24 Annually Employment Type 2 - Staff: Career Duration Indefinite

Primary Duties and Responsibilities

Press space or enter keys to toggle section visibility

Job Qualifications

Required:

  • Bachelor's Degree or three-to seven years of study coordination or clinical research coordination experience
  • Ability to work efficiently and complete tasks with a high degree of accuracy.
  • Ability to organize multiple projects for efficiency and cost-effectiveness.
  • Analytical skills sufficient to work and solve problems.
  • Ability to work flexible hours to accommodate research deadlines.
  • Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.
  • Ability to be flexible in handling work delegated by more than one individual or in the course of delegating work.
  • Strong interpersonal communication skills to effectively and diplomatically interact with others, including institutional leadership.
  • Strong written communication skills, ability to compose advanced correspondence and manage large file systems.
  • Advanced typing and computer skill/ability including word-processing, use of spreadsheets, email and data entry.
  • Ability to handle confidential material with judgement and discretion.
  • Skill in managing diverse, complex tasks and information transfer among multiple constituents.
  • Sufficient math ability and knowledge of clinical trials budgeting processes to manage the preparation of clinical trial budgets.
  • Advance knowledge of the clinical research regulatory framework and institutional requirements.
  • Ability to supervise and delegate clerical work as needed.
  • Advanced knowledge of Good Clinical Practice (GCP) for clinical research.
  • Strong knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
  • Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc
University of California
Vacancy posted 6 days ago
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