Research Assistant 1, Per Diem
The University of Miami
Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review this tip sheet. The UHealth system at the University of Miami has an exciting opportunity for a Per Diem - Part Time Research Assistant 1 in the Public Health Sciences Department. This position is located in the Health District. SUMMARY The Research Assistant 1 (A) contributes to research investigators by providing research and experimentation support while following established protocols. The Research Assistant 1 (A) performs a clerical role to ensure the smooth operations of office facilities. CORE JOB FUNCTIONS
Part time Employee Type:
Temporary Pay Grade:
A1
- Sets up and operates various scientific apparatus and makes minor repairs.
- Prepares correspondence and answers phones.
- Formulates and maintains bibliographies and completes applications and forms.
- Orders laboratory supplies and maintains culture media reagents.
- Reviews and edits various materials for publication and prepares publication schedules.
- Maintains appropriate logs, records, and study notebooks.
- Adheres to University and unit-level policies and procedures and safeguards University assets.
- Skill in completing assignments accurately and with attention to detail.
- Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
- Ability to process and handle confidential information with discretion.
- Ability to work evenings, nights, and weekends as necessary.
- Commitment to the University's core values.
- Ability to work independently and/or in a collaborative environment.
- Organizes and maintains a system for monitoring of subjects enrolled on longitudinal studies and assures collection of data in a timely manner.
- Prepares and organizes data to promote efficient computer entry. Demonstrates knowledge of Good Clinical Practice Guidelines, IRB review, reporting requirements and regulatory affairs.
- Oversees schedule and follows-up on progress in patient's chart and performs retrospective chart reviews.
- Participates in the consent process as guided by institutional policy and assists with the development of the consent forms.
- Communicates with internal and/or external regulatory oversight entities (e.g. IRB, NIH).
- Participates in the development of protocol roadmaps or flow sheets and may participate in the completion of reports and forms.
- Strong bilingual (English and Spanish) reading, writing and oral communication skills preferable.
Part time Employee Type:
Temporary Pay Grade:
A1
Vacancy posted 3 days ago
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