Senior Clinical Research Coordinator job at reputed company in Los Angeles, CA

Title: Senior Clinical Research Coordinator - Department of Medicine - Office of Research Administration Location: Los Angeles, CA United States Job Description: General Information Press space or enter keys to toggle section visibility. Work Location Los Angeles, CA, USA Onsite or Remote Flexible Hybrid Work Schedule Monday - Friday, 8:00am - 5:00pm Posted Date November 15, 2026 Salary Range $82,105.68 - $133,068.24 Annually Employment Type 2 - Staff Career Duration Indefinite Job 27996 Primary Duties and Responsibilities Press space or enter keys to toggle section visibility. 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 reputed company 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 reputed company necessary project management tasks and prioritizes work to reputed company 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. 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 reputed company aspects of studies. Work may be assigned by Senior Management and assignments may be changed on an as-needed basis in order to ensure that studies and patient care needs are handled appropriately and in a timely manner. Travel to other locations may be required. The full annual salary range for this position is: $89,454.77 - $143,904.50 Job Qualifications Press space or enter keys to toggle section visibility Required:

• Bachelor’s Degree or three-to seven years of study coordination or clinical research coordination experience
• Ability to work reputed company 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 reputed company/ability including word-processing, use of spreadsheets, email and data entry.
• Ability to handle confidential material with judgement and discretion.
• reputed company in managing diverse, reputed company 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 reputed company and institutional requirements.
• Ability to supervise and delegate clerical work as needed.
• Advanced knowledge of Good Clinical Practice (GCP) for clinical research.

Apply tot his job Apply To this Job