Site Management Associate I

PSI CRO·Buenos Aires, Buenos Aires, Argentina

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About the role

Supports clinical research projects in Buenos Aires by coordinating communication between sites, CRAs and vendors; managing CTMS, TMF and ISF documentation; overseeing clinical supplies, regulatory submissions, training, audits and safety information flow. Requires a college/university degree in Life Sciences, English proficiency, MS Office proficiency, local regulations knowledge, and clinical research-related experience, with CTA/CRO experience preferred.

Key requirements

• College/University Degree in Life Sciences
• Required skills: Clinical research support, Site communication and coordination, Query resolution, EDC completion support, Vendor and study supply coordination, Clinical supplies management, CTMS management, Regulatory and ethics committee submissions and notifications, Audit and inspection preparation, Trial Master File (TMF) management, Investigator Site File (ISF) management, Project training coordination, Document management, Safety information flow, Local regulations knowledge, English language proficiency, MS Office proficiency, Planning, Communication, Collaboration
• Required language: English

Opportunity details

• Workplace: Hybrid
• Posted: Sep 18, 2026
• Original advert language: English

Full vacancy

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Employer’s role description

Job title: Site Management Associate I

Location: Buenos Aires, Buenos Aires, Argentina

Employment type: Full-time

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 2,800 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

Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.

Only CVs in English will be accepted.

You will be responsible for:

Being the main point of contact between site personnel and CRA involved in the project helping on query resolution and EDC completion.
Serves as the primary sites’ contact point for vendors, study supplies, and access management.
Ensure that pre-study testing (scans, MRI/CT qualification questionnaires, test ECGs, etc.) of local site facilities is completed.
Assists the Monitors in their prompt completion of all subject event and site event information in CTMS. Track the resolution status of site issues and action items in CTMS.
Act as the one who will ensure the order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies.
Ensures regulatory and ethics committee submissions and notifications, meaning you will need to be up to date on local regulations and dispositions.
Coordinate preparation for and follow-up on site, TMF and systems´ audits and inspections.
Manage the TMF on a site and a country level for regularly and file documents. Prepare, distribute, and update Investigator Site Files (ISF) and ISF checklists.
Arrange and track initial and on-going project training for site teams in all vendor-related systems.
Document Management and translations status review of the study.
Ensures proper safety information flow with investigative sites.

Qualifications

College/University Degree in Life Sciences;
Administrative work experience, preferably in an international settings;
Prior experience working as CTA for CROs;
Prior experience working in Clinical Research;
Local regulations knowledge;
Full working proficiency in English;
Proficiency in MS Office applications;
Ability to plan and work in a dynamic team environment;
Communication and collaboration skills.

Additional Information

Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.