Senior Clinical Research Coordinator (Flexible Hybrid)

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.