Jobs · Administrative · Texas

Site Management Associate II

PSI CRO · Austin, TX · 2 wk ago
HybridAdministrativeFull-time

About the role

Start your career in clinical research, streamlining communication, maintaining systems and managing documents.

Responsibilities

  • Main site contact for all non-trial-participant related and non-protocol related issues, including vendors, trial supplies and access management
  • Manages records flow with sites and off-site facilities
  • Prepares regulatory and ethics committee submission/notification documents and records
  • Coordinates payments to sites and off-site facilities
  • Prepares for and follows up on site audits and inspections
  • Reviews and coordinates site-specific query resolution with Monitors and sites
  • Reviews site-specific EDC completion progress and provides the Monitor with regular updates
  • Serves as the main contact point for other company departments in administrative site-related issues
  • Organizes, participates in, and prepares reports of internal project team meetings
  • Collaborates with sites and project team on Investigator Meetings' organization
  • Under supervision, provides on-the-job coaching of Site Management Associates I and Clinical Operations Administrative Support staff
  • Arranges and tracks initial and ongoing trial training for investigator site teams in all vendor-related systems
  • Provides training in courier management and trial supplies ordering to the investigator sites
  • Files trial records in the TMF and performs regular TMF checks on a site and country level
  • Participates in and follows up on TMF and systems audits
  • Prepares, distributes, and updates Investigator Site Files (ISF) and ISF checklists
  • Coordinates the translation process for trial records on a site and country level
  • Collects IP-REDs and compiles IP-RED packages for further review

Qualifications

  • College or university degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities is considered sufficient
  • Minimum 2 years experience within the clinical research industry, corporate or academic environment where administrative experience and technical skills have been gained
  • Basic proficiency in MS Word, MS Excel, MS Outlook, and MS PowerPoint
  • Knowledge (following proper training) of applicable software and project specific systems
  • Basic typing skills in English (min. 40 words per minute)

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