Senior Site Management Associate
- Location
- US, US, United States
- Work mode
- Remote
- Employment type
- Full-time
About the job
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Job Description 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 & II 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
- Main vendor contact for all non-trial participant related issues, including pre-trial testing of vendor systems
- Tracks vendor-related supplies on a site, country/regional level
- Exchanges information and records with vendors
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 3-year experience within the clinical research industry, CRO preferred, in similar role or equivalent to Site Management Associate II
- 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.
Additional Information Become a full-fledged clinical research professional with the support of a knowledgeable and professional team. You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects. For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.
From PSI CRO's careers page (SmartRecruiters), checked 29 Oct 2026.
How to apply
- Select Apply on jobs.smartrecruiters.com. It opens PSI CRO's own application form in a new tab, run on SmartRecruiters.
- Fill in the form and upload your résumé there. Jobiwork never sees your application.
- PSI CRO will reply to you directly. No real employer asks you for money to apply.
Posted 29 Oct 2026 · checked 29 Oct 2026 · Report this job