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NCIRE - The Northern California Institute for Research and Education, Inc. · 2 months ago

Staff Research Associate IV, Supervisor

San Francisco, CA

Full-time

Hybrid

Senior Level, Lead/Staff

$69K/yr - $120K/yr

5+ years exp

NCIRE - The Northern California Institute for Research and Education, Inc. is seeking a Staff Research Associate IV, Supervisor. This role involves overseeing a diverse portfolio of research activities, including managing clinical trials and supervising a research team, while ensuring compliance with regulatory and budgetary standards.

BiotechnologyHealth CareMedicalNon Profit

No H1B

U.S. Citizen Only

Responsibilities

Directly supervises the planning, development, implementation, running, and management of clinical trials at the SFVA Hematology/Oncology Research Program

Exercises supervisory authority, including hiring, transferring, suspending, promoting, managing conduct and performance, discharging, assigning, rewarding, disciplining, and/or approving hours worked of at least 3 to 6 full-time equivalent (FTE) employees

Manages, assigns, and performs clinical trial project coordination services for Principal Investigator

Provides assistance with managing Principal Investigator lab and biospecimen studies and coordinating cross-cutting efforts of bench science with clinical trials

Contributes to the development of protocols, related documents, manuscripts, and Case Report Forms

Implements quality assurance standards and compliance in regulatory and budgetary areas of the clinical trials

Qualification

Clinical trial managementResearch project managementRegulatory complianceBudget managementEmployee supervisionOrganizational skillsCommunication skillsAttention to detailFlexibility

Required

Master's degree or Bachelor's degree with relevant supervisory or budget management experience required

At least two years of research project management experience

At least two years of employee supervision experience

At least 2 years of industry trial experience

At least 2 years of regulatory work experience in clinical trials

Excellent organizational and communication skills (both written and verbal)

Strong attention to detail

Flexibility to work both independently and collaboratively

Understand critical aspects of project management including tracking, enrollment, retention, regulatory compliance, data management and staff supervision