Jobs at PSI CRO

Supports clinical trial site operations by coordinating site and vendor communication, clinical supply management, regulatory and ethics submissions, CTMS/EDC documentation, TMF/ISF maintenance, training, vendor qualification tracking, audit preparation, and serving as primary site contact for study logistics and safety information.

Contribute to statistical programming for global clinical trials: develop analysis datasets, write program specs, produce Tables/Listings/Figures (TFLs), validate SAS programs, prepare documentation, and liaise with project teams.

Support clinical research projects by managing communication, documents, and inventory related to clinical supplies and site management, ensuring compliance and organization.

The Director of Business Development will expand the client base, develop business plans, manage sales processes, and maintain customer satisfaction in the medical research field.

Provide administrative and operational support for clinical trial sites: manage supplies, regulatory submissions, CTMS/EDC/TMF records, vendor and site communications, training, and audit preparation.

The Site Management Associate II will manage site communication, documentation, and training in clinical research, ensuring compliance and efficiency.

The Site Coordinator supports clinical study activities, acts as a liaison, tracks patient enrollment, and manages study documentation and data entry.

The role involves managing site communications, document management, and training in clinical research, serving as a liaison with sites and vendors.

Verify and process country expense reports, ensure compliance with company and client requirements, produce accrual and cumulative passthrough reports, perform reconciliations at project close or termination, and complete administrative and clerical tasks supporting project teams.

Manage clinical trial data including eCRF design, EDC testing, data entry/validation, SAE reconciliation, coding, metrics tracking to database lock, QC checks, audits, and training site staff on data management processes.

Lead local clinical site operations, build relationships with sponsors/CROs and investigators, assess study feasibility, supervise trials per ICH-GCP, manage budgets and timelines, promote and expand site network, support marketing, and represent the company at conferences and meetings.

Provide site management support for clinical trials: manage site communication, clinical supplies, regulatory/ethics submissions, TMF/ISF and document control, CTMS/EDC updates, safety information flow, audit preparation, and coordination of meetings and vendor/site payments.

Lead strategy and expansion of PSI's clinical trial operations in Thailand/APAC: develop operational growth plans, identify and evaluate sites, maintain site databases, monitor market and competitor trends, build stakeholder relationships, analyze enrollment feasibility and performance, support feasibility processes with Operations, and represent PSI at scientific conferences.

Provide administrative and document management support for clinical research projects: exchange project data, manage clinical supplies, maintain TMF/OSF, assist audits, support meetings, and ensure safety information flow between sites and project teams.

Lead country-level study activation, manage startup tracking systems, support contracts and budgets, collect regulatory documents, prepare submissions under supervision, communicate with sites and project teams, develop site timelines, review translations, and supervise TMF maintenance during startup.

Lead strategy and expansion of clinical trial operations in Malaysia and APAC. Identify and evaluate sites, build site databases, monitor market and competitors, support feasibility and enrollment, cultivate stakeholder relationships, and represent PSI at scientific meetings.

Hybrid BA/Developer who gathers stakeholder requirements, designs and builds database structures and Power BI reports, writes and optimizes SQL, supports Agile delivery, testing, deployments, and UAT to deliver accurate, scalable data solutions.

Provide clinical sites with technical support for study technologies (MRI, nuclear medicine, radiology); design and implement study-related technology forms and manuals; coordinate imaging data collection and documentation; organize technical training; perform site initiation and technical visits; advise site monitors and communicate technical resource needs.

Provide daily technical support for desktop systems and peripherals: troubleshoot and diagnose issues, handle support requests, install/configure and maintain hardware, manage asset inventories and licensing, document problems/resolutions, and assist with basic IT training.

Lead business development in Japan for a global CRO: prospect and manage enterprise accounts, develop sales strategies and proposals, lead pitches, coordinate with Operations and Project teams, negotiate contracts and changes in scope, maintain client relationships, monitor satisfaction, and ensure successful hand-offs to project teams.