Clinical Research Technician, MOSAAIC Study of Asian Americans

* Coordination and management of quality control for observational and interventional, including both clinic and community-based studies, within the Institute for Population and Precision Health.
* This may include multi-institutional and some international studies, many of which are federally funded or funded by pharmaceutical sponsors.
* Includes oversight of the collection of clinical data, survey data, environmental data, and associated samples and biospecimens.
* Assist with subject engagement, screening, recruitment, consent, data and specimen collection, and subject follow-up and retention activities primarily at the location of our community partners.
* Monitor study participants, schedule, and conduct study-related procedures (eg. interviews, phlebotomies, and follow-ups) and establish data quality control checks).
* Work with the Scientific Directors and Research Manager in the planning, development, and evaluation of research.
* Coordination of data acquisition, entry, QC, and query response.
* Assist in the preparation of presentations, media and curricular materials relating to research.
* Accountable for all tasks in moderately complex clinical studies.
* Facilitates and participates in the daily activities of moderately complex clinical studies and performs various activities including patient data retrieval, documenting clinical research records, and participation in program audits.
* Performs all tasks in moderately complex clinical studies.
* Assists with and performs various administrative and operational tasks under direct supervision.
* Participates in the daily activities of moderately complex clinical studies and performs various activities including patient data retrieval, documenting clinical research records, and participation in program audits. Contributes to the problem solving on assigned clinical research studies and tasks.
* Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples.
* Performs other related work as needed.
* 2–5 years of experience in clinical research coordination, management, or a related role.
* Experience overseeing observational and interventional studies, including multi-institutional or international research projects.
* Strong knowledge of clinical research methodologies, data collection, and analysis techniques.
* Understanding of IRB processes, regulatory policies, and compliance requirements.
* Ability to maintain accuracy and consistency in data management, documentation, and reporting.
* Strong analytical and critical thinking skills to identify issues, develop solutions, and implement improvements.
* Ability to manage multiple tasks, projects, and deadlines effectively.
* Excellent verbal and written communication skills for collaboration with study teams, participants, and stakeholders.
* Capability to train, mentor, and supervise frontline research staff.
* Ability to work collaboratively in a multidisciplinary research environment while maintaining independence.
* Skilled in Microsoft Office and relevant research software applications.
* Competence in recruiting, consenting, and retaining study participants while ensuring a positive experience.

When applying, the document(s)
** MUST
* * be uploaded via the
** My Experience
** page, in the section titled
** Application Documents
** of the application.

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