Project Staff Assistant

Stony Brook Medicine

Stony Brook, NY, United States1w ago

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Key details

Location
Stony Brook, NY, United States
Work style
Onsite
Level
Entry level
Job type
Full-time
Experience
3–6 yrs
Function
Administrative
Focus area
other
Posted
1w ago

Skills

budgetingexcelgcphipaamicrosoft officemicrosoft wordregulatory compliance

About the role

Required Qualifications (as evidenced by an attached resume):

Bachelor’s degree (foreign equivalent or higher) in Public Health, Health Administration, Biological Sciences, Research Administration, or a related field. Three (3) years of full-time experience in research administration or grant management in an academic or healthcare research environment. Working knowledge of NIH, foundation funding mechanisms, and federal compliance requirements. Experience with grant submission platforms (e.g., Grants.gov, ASSIST, eRA Commons, ProposalCentral.com, institutional routing systems) and forms (e.g., SciENcv, NIH biosketch formats). Proficiency with Microsoft Office (especially Excel and Word). Experience managing IRB submissions, regulatory compliance activities, and clinical research operations in an academic medical center or healthcare research setting. Working knowledge of federal regulations related to human subject’s research, including IRB requirements, HIPAA compliance, and/or clinical trial SOPs.

Preferred Qualifications:

Master’s degree in public health, Business, Research Administration, or related field. Five (5) or more years of full-time experience in research administration or grant management in an academic or healthcare research environment. Grants’ management certification (e.g., GPC, GMCP, CGMS) by start date. Experience with OBGYN or Women’s Health Research. Familiarity with post-award management, effort reporting, and subcontract management. Experience supporting multi-investigator or multi-site grant applications. Experience with clinical trial oversight and management in an academic medical center or healthcare setting, including regulatory compliance and study operations.

Brief description of duties:

Provide comprehensive pre-and-post award grant administration, research compliance, and regulatory support for departmental research activities. Manage funding applications, post-award processes, IRB submissions, and compliance requirements while serving as a liaison between investigators, sponsors, and institutional offices to support the successful conduct of research programs. The ideal candidate will have strong budgeting, organizational, and project-management skills including high attention to detail. The ideal candidate will have Strong budgeting, organizational, and project-management skills including high attention to detail.

Duties:

Grant administration

  • Monitor and identify relevant federal, foundation, and industry funding opportunities for OBGYN faculty and research teams.

  • Support preparation of grant applications, including budget development, biosketches, facilities/other resources, and required documentation.

  • Coordinate internal routing and ensure compliance with institutional, sponsor, and regulatory requirements.

  • Serve as primary liaison with the institution’s grants and contracts office, sponsors, and collaborating departments.

  • Manage post-award activities such as reporting, budget tracking, effort monitoring, and award modifications.

  • Assist faculty and trainees with research administration needs, timelines, and best-practice guidance.

  • Maintain organized grant records, deadlines, and shared resources for the department.

Human Subjects Research Regulatory Compliance

  • Coordinate and support Institutional Review Board (IRB) submissions, including initial applications, amendments, continuing reviews, reportable events, study closures, and related regulatory documentation.

  • Ensure research projects maintain compliance with IRB, HIPAA, Good Clinical Practice (GCP), institutional policies, and applicable federal regulations governing human subjects’ research.

  • Serve as a liaison between investigators, the IRB office, compliance offices, and study teams to facilitate timely regulatory approvals and renewals.

  • Maintain regulatory binders, approval records, consent documents, and study-related compliance documentation to support audits and monitoring activities.

  • Track regulatory deadlines and provide investigators with proactive guidance regarding IRB submissions, approvals, and reporting requirements.

Advance OBGYN Research mission

  • Identify, research and analyze issues within Research Division operations for senior leadership and Department Chair

  • Work with staff to publicize and disseminate research findings

  • Build cross-departmental collaborations to advance interdisciplinary research

Other duties as Assigned

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