Senior Clinical Research Coordinator, Santa Monica

The
Senior Clinical Research Coordinator plays a critical role in the overall
operational management of clinical research/trial/study activities from design,
set up, conduct, through closeout. The ideal candidate is an experienced
professional or leader who has direct responsibility for the implementation of
research activities for one or more studies which may include multicenter
clinical trials (both NIH and industry-sponsored), local investigator-initiated
clinical trials, and/or programmatic clinical research activities. Recognize
and perform necessary project management tasks and prioritizes work to reach
scheduled goals. The Senior Clinical Research Coordinator is a technical leader
responsible for ensuring the study protocol and procedures have been completed
accurately, safely, and in a timely manner. This position may supervise and
train others on projects as necessary. Work with PIs, departments, sponsors,
institutions, and other entities as needed to support and provide guidance on
the administration of the compliance, financial, personnel and other related
aspects of studies.

Salary
offers are determined based on various factors including, but not limited to,
qualifications, experience, and equity. The full annual salary range for this
position is: $82,713.61 - $133,060.10

Required:

• Bachelor's Degree or three-to seven years of study coordination or
  clinical research coordination experience
• 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.
• 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.