Job Summary
The Senior Site Management Associate acts as the main liaison for various site-related administrative matters, which encompass vendor collaboration, management of trial materials, and oversight of access protocols. This position involves handling regulatory documentation, conducting site audits, maintaining the Trial Master File (TMF), and offering guidance to junior personnel.
Responsibilities
- Serve as the principal point of contact for administrative concerns related to the site.
- Coordinate vendor activities and manage trial supplies efficiently.
- Handle access management to ensure appropriate site entry and security.
- Oversee the maintenance of regulatory documentation and support site audits.
- Ensure proper upkeep of the Trial Master File (TMF).
- Provide coaching and support to junior team members.
Qualifications
- A college or university degree is required.
- Minimum of 3 years of experience in the clinical research field, ideally within a Contract Research Organization (CRO).
- Strong proficiency in Microsoft Office applications.
- Capability to manage regulatory tasks and administrative duties tailored to site requirements.
PSI CRO provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
