ECHO Research Associate 3

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CORE JOB SUMMARY
The Research Associate 3 GAB assumes responsibility for the design and performance of research focused on the development of novel experimental therapies for assigned area. The incumbent contributes to collaborations with scientists within the University of Miami or elsewhere. Moreover this individual works as part of a team and assists with the maintenance of laboratory equipment protocols and supplies.

The Research Associate 3 (RA III) ECHO provides advanced research support for the Environmental Influences on Child Health Outcomes (ECHO) study through a combination of clinical operations participant-based research activities and laboratory support.

This role is responsible for coordinating study visits supporting participant scheduling and engagement conducting protocol-driven research activities and assisting with biospecimen collection and processing. The Research Associate 3 ensures accurate compliant and efficient execution of study protocols across clinical and laboratory settings while supporting research staff and maintaining consistency in workflows.

CORE JOB FUNCTIONS
1. Maintains daily operations and performs procedures related to new and on-going research projects.
2. Assists with ordering purchasing and maintenance of all required reagents and supplies for laboratory activities and monitors and maintains inventory of supplies and stocks.
3. Assists with the maintenance of institutional biosafety and animal care protocols laboratory safety records and standard operating procedures.
4. Performs and assists other research staff with standard laboratory techniques.
5. Develops adapts and implements new laboratory procedures.
6. Records organizes and writes up experimental results for submission of manuscripts and for scientific presentations.
7. Keeps abreast of latest literature in the field and searches for references to technical problems.
8. Maintains current knowledge of the methods and techniques related to the specific field of research.
9. Adheres to University and unit-level policies and procedures and safeguards University assets.

This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.

CORE QUALIFICATIONS
Education:
Bachelors degree in relevant field required

Experience:
Minimum 5 years of relevant experience required

Certification and Licensing:
Refer to department description for applicable certification requirements

Knowledge Skills and Abilities:

• Learning Agility: Ability to learn new procedures technologies and protocols and adapt to changing priorities and work demands.
• Teamwork: Ability to work collaboratively with others and contribute to a team environment.
• Technical Proficiency: Skilled in using office software technology and relevant computer applications.
• Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.

Department Job Functions

Coordinates clinical study activities including participant scheduling visit flow and protocol adherence

Maintains and manages participant scheduling systems to ensure efficient coordination of study visits

Conducts participant study visits and research activities in accordance with study protocols

Performs data collection procedures including surveys assessments and study instruments

Supports participant recruitment scheduling and follow-up to maintain engagement and retention

Assists with biospecimen collection labeling handling processing storage and shipment

Maintains accurate documentation of participant data study activities and biospecimen tracking in research systems

Ensures compliance with study protocols regulatory requirements and biosafety standards

Maintains chain-of-custody for biospecimens and ensures proper handling procedures

Coordinates with clinical laboratory and operations staff to ensure seamless execution of study activities

Provides training and guidance to research assistants on study procedures workflows and participant interaction

Supports onboarding and ongoing training of research staff

Monitors study workflows and identifies issues related to scheduling visit execution data integrity or laboratory processes

Assists in the implementation and improvement of study procedures and workflows

Maintains inventory of study materials laboratory supplies and data collection tools

Communicates operational or workflow concerns to leadership as appropriate

Adheres to University and unit-level policies and procedures and safeguards University assets

DEPARTMENT ADDENDUM

1. Clinical Scheduling and Coordination

• Coordinate participant scheduling and manage study visit calendars
• Ensure accurate tracking and completion of study visits
• Adjust schedules based on participant and staffing needs

2. Study Visit Execution

• Conduct participant study visits and protocol-driven procedures
• Perform data collection and ensure accurate documentation
• Support participant engagement and retention

3. Laboratory and Biospecimen Support

• Process biospecimens in accordance with study protocols
• Maintain accurate labeling tracking and storage of samples
• Support laboratory workflows and compliance with biosafety standards

4. Research Staff Training and Support

• Train research assistants on study procedures and workflows
• Provide ongoing guidance to ensure consistency and quality
• Support onboarding of new research staff

5. Workflow Monitoring and Compliance

• Monitor study workflows for efficiency and protocol adherence
• Identify and communicate operational or compliance concerns
• Support audit readiness and proper documentation practices

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