Full-Time

Site Manager

Irvine Clinical Research

Irvine Clinical Research

Compensation Overview

$100k - $120k/yr

Inglewood, CA, USA

In Person

Category
Operations & Logistics (1)
Requirements
  • Demonstrated success in managing a research site, specifically with complex clinical drug trials.
  • Exceptional attention to detail and proven ability to manage multiple high-priority tasks simultaneously.
  • Excellent communication skills, both written and verbal.
  • Track record of building, motivating, and sustaining a cohesive team.
  • Strong interpersonal, customer service, and hands-on problem-solving skills.
Responsibilities
  • Lead Site Operations: Oversee the entire research site, acting as the primary problem-solver for all day-to-day and ad-hoc operational needs.
  • Team Management: Direct and motivate a team poised for significant, immediate growth across clinical investigators, coordinators, and staff. This includes hiring (with network support), onboarding, scheduling, and performance evaluations.
  • Drive Financial & Enrollment Goals: Ensure the site meets all targets for participant enrollment, financial growth, and long-term business sustainability.
  • Clinical Study Oversight: Be accountable for the successful execution and participant recruitment for all clinical studies conducted at the site.
  • Compliance and Quality: Maintain data integrity and quality across all electronic systems (eSource, EDC, CTMS). Own the successful completion of regulatory requirements and sponsor monitoring visits.
  • Strategic Communication: Serve as the key liaison to site network management to implement strategic initiatives and coordinate with local partners for services like community outreach and imaging.
  • Relationship Management: Foster effective working relationships with all stakeholders: study participants, Sponsors/CROs, and staff.
Irvine Clinical Research

Irvine Clinical Research

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