Senior Clinical Research Coordinator
Job Description
UCLA
Internal Number: 144808691
The Department of Medicine’s Lung Cancer Research Program is looking to a hire an experienced Senior Clinical Research Coordinator to play a vital role in managing and executing complex clinical trials and research initiatives, including multicenter NIH and industry-sponsored studies, investigator-initiated projects, and programmatic research. This position ensures all protocols are implemented accurately, safely, and on schedule while overseeing compliance, financials, and personnel. As a technical leader, you will collaborate with PIs, departments, sponsors, and institutions, as well as mentor and train team members. This role is essential to supporting the Department’s growing portfolio of newly awarded and ongoing grants, driving impactful advancements in lung cancer research.
Annual range: $82,713.61-$133,060.10
- Bachelor’s Degree or three-to seven years of study coordination or clinical research coordination experience
- Ability to work efficiently 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 skill/ability including word-processing, use of spreadsheets, email and data entry.
- Ability to handle confidential material with judgement and discretion.
- 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.
Source ⇲
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