Research Center Administrator - Biochemistry & Grants Lead

University of Vermont

Colchester (VT)

On-site

USD 110,000 - 117,000

Full time

14 days+

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Job summary

University of Vermont is seeking a Research Program Admin MG4 X to define, develop, and lead a robust research enterprise centered on grants, contracts, and fee-for-service work. You will oversee grant preparation, budgets, protocols, and daily LCBR operations, supervising senior staff to maintain timelines and priorities for technical teams.

The role requires a Master’s degree in biochemistry, epidemiology, or related field, plus 4–6 years of related experience in clinical labs or research

Qualifications

  • Master’s degree in biochemistry, epidemiology, or related field.
  • Four to six years’ related experience including administrative experience in a clinical laboratory or clinical research setting.
  • Experience designing and implementing large-scale clinical trials and/or epidemiological studies.
  • Experience with budget building and extramural training; preparing Manuals of Operations; supplying phlebotomy kits.

Responsibilities

  • Define, develop, implement, and lead a robust research enterprise with grants, contracts, and a fee-for-service account.
  • Perform grant preparation, budget creation and management, and protocol development.
  • Oversee daily operations of the Laboratory of Clinical Biochemistry Research (LCBR) and supervise senior staff.
  • Act as key contact for outside agencies, representing the LCBR and making decisions for principal investigators.

Skills

Grant management
Budget planning
Supervisory experience
Clinical research design
SPSS

Education

Master’s degree in biochemistry/epidemiology or related field

Tools

SPSS

Job description

University of Vermont is seeking a Research Program Admin MG4 X to define, develop, and lead a robust research enterprise centered on grants, contracts, and fee-for-service work. You will oversee grant preparation, budgets, protocols, and daily LCBR operations, supervising senior staff to maintain timelines and priorities for technical teams.

The role requires a Master’s degree in biochemistry, epidemiology, or related field, plus 4–6 years of related experience in clinical labs or research

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