Site Management Associate II
King of Prussia, United States · Full-time
- Posted 2w ago
- From PSI CRO AG’s careers page
- Location
- King of Prussia, United States
- Type
- Full-time
- Level
- Entry Level
- Experience
- 2+ years
- Department
- Business Operations
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About the role
Job Description
Start your career in clinical research, streamlining communication, maintaining systems and managing documents.
The scope of responsibilities will include:
- 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 year experience within the clinical research industry, corporate or academic environment where administrative experience and technical skills have been gained.
- Basic proficiency in MS Word.
- Basic proficiency in MS Excel.
- Basic proficiency in MS Outlook.
- Basic proficiency in MS Power Point.
- 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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About PSI CRO AG
A global CRO for clinical trialsPSI CRO is a global contract research organization that manages clinical trials, with expertise in pivotal Phase 2 and Phase 3 studies.
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