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.