Asheville, North Carolina, North Carolina
Bossier City, Louisiana
Cary, North Carolina
Mitchell, South Dakota
Posted: 15-Jul-24
Location: Torrance, California
Salary: Open
Categories:
Internal Number: 140056101
TheSenior Clinical Research Coordinator plays a critical role in the overalloperational management of clinical research/trial/study activities from design,set up, conduct, through closeout. The ideal candidate is an experiencedprofessional or leader who has direct responsibility for the implementation ofresearch activities for one or more studies which may include multicenterclinical trials (both NIH and industry-sponsored), local investigator-initiatedclinical trials, and/or programmatic clinical research activities. Recognizeand perform necessary project management tasks and prioritizes work to reachscheduled goals. The Senior Clinical Research Coordinator is a technical leaderresponsible for ensuring the study protocol and procedures have been completedaccurately, safely, and in a timely manner. This position may supervise andtrain others on projects as necessary. Work with PIs, departments, sponsors,institutions, and other entities as needed to support and provide guidance onthe administration of the compliance, financial, personnel and other relatedaspects of studies.
Salaryoffers are determined based on various factors including, but not limited to,qualifications, experience, and equity. The full annual salary range for thisposition is: $82,713.61 - $133,060.10
Required:
- Bachelor's Degree or three-to seven years of study coordination orclinical 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 thatcontains distracting stimuli and competing deadlines.
- Ability to be flexible in handling work delegated by more than oneindividual or in the course of delegating work.
- Skill in managing diverse, complex tasks and information transferamong multiple constituents.
- Sufficient math ability and knowledge of clinical trials budgetingprocesses to manage the preparation of clinical trial budgets.
- Advance knowledge of the clinical research regulatory frameworkand institutional requirements.
- Ability to supervise and delegate clerical work as needed.
- Advanced knowledge of Good Clinical Practice (GCP) for clinicalresearch.
