Description Are you passionate about clinical research and looking to make a meaningful impact? Join our dynamic team as a Study Coordinator, where you'll play a key role in driving innovative research and improving patient outcomes. In this exciting position, you'll oversee every phase of clinical trials-from study design and initiation to execution and closeout-focused on Hereditary Hemorrhagic Telangiectasia (HHT) projects. As a vital part of our team, you'll: + Manage research activities + Prioritize tasks + Ensure deadlines are met while maintaining full compliance with protocols and regulatory standards. collaborate with Principal Investigators, research teams, sponsors, and stakeholders to ensure smooth operations + Compliance and financial management to staffing support. This is your chance to be part of groundbreaking work in a fast-paced, impactful environment where your contributions truly matter. Salary: $33.63 - $54.11 hourly Qualifications Required: + Bachelors Degree or equivalent experience/training + Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships. + Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness. + Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines. + Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines. + Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications. + Ability to handle confidential material information with judgement and discretion. + Working knowledge of Institutional Review Board review and reporting requirements, institutional committee application and approval process, Contracts and Grants and departmental policies and procedures. Working knowledge of Institutional Review Board and Internal Scientific Peer Review Committee. + Working knowledge of FDA Code of Federal Regulations and ICH good clinical practices for clinical research. + Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc. Preferred: + 1-3 years of study coordination experience + Bilingual (English and Spanish) UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.