University of Miami

Healthcare

Sr.ResearchAssociate1

$1–1k Miami, Florida, United States FULL TIME
The Brief

“Sr. Research Associate 1 at University of Miami. Skills: Research coordination, Protocol implementation, Staff supervision, Data quality. Collect research data. Analyze research data”

Industry & Context.

Healthcare
Problems you'll solve

Analyze problems; Solve problems

Eligibility Requirements

Occasional evening hours, Occasional weekend hours, Travel to research sites, Light lifting

What They're Looking For.

Must Have

Master's degree required, Demonstrated leadership experience, Proficiency in Microsoft Office, Experience with REDCap, Experience with EPIC/Cerner, Knowledge of IRB procedures, Knowledge of federal regulations, Knowledge of data privacy standards

Nice to Have

Master's degree in public health, Master's degree in social work, Master's degree in psychology, Fluency in Spanish, Fluency in Haitian Creole, Experience with underserved communities, Experience conducting health disparities research, Phlebotomy certification, Experience collecting biological samples, Experience with NVivo, Experience with rapid analysis techniques, Knowledge of medical terminology, Knowledge of medical record abstraction

What You'll Do.

Collect research data

Analyze research data

Present research data

Maintain research databases

Interpret research protocols

Participate in publication

Maintain current knowledge

Ensure good research practice

Ensure compliance with guidelines

Safeguard University assets

Lead research studies

Coordinate research studies

Manage research protocols

Ensure regulatory compliance

Oversee implementation

Supervise recruitment

Supervise data collection

Manage stakeholder relationships

Conduct performance assessments

Support professional development

Ensure standardization

Develop recruitment strategies

Conduct informed consent

Collect biological specimens

Maintain participant relationships

Maintain community relationships

Oversee IRB submissions

Prepare IRB documents

Submit IRB amendments

Submit adverse event reports

Submit protocol deviations

Ensure research compliance

Maintain documentation

Ensure regulatory binders complete

Monitor data integrity

Conduct qualitative analysis

Coordinate data analysis

Maintain participant records

Prepare enrollment summaries

Prepare interim reports

Prepare project deliverables

Coordinate grant reporting

Schedule team meetings

Prepare meeting agendas

Ensure follow-up on action items

Monitor study supplies

Collect biological specimens

Coordinate laboratory drop off

Coordinate laboratory storage

Adapt to project needs

Travel to research sites

How You'll Work.

Team & Collaboration

Multidisciplinary research team; Junior research staff; Community partners; Funding agencies; Principal Investigators; Internal stakeholders; External stakeholders; Collaborators; Sponsors; Regulatory offices

Communication Scope

Written communication; Verbal communication; Scientific monographs

Process & Methodology

Protocol implementation, Timeline management, Budget management

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