PSI CRO

Burlingame
Total Offices: 3
1,939 Total Employees
Year Founded: 1995

Jobs at PSI CRO

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Recently posted jobs

18 Days AgoSaved
Hybrid
Austin, TX, USA
Pharmaceutical
Provide site administrative support for clinical trials: act as main non-clinical site contact, manage records and TMF/ISF processes, prepare regulatory submissions, coordinate payments, support audits, track EDC completion, organize meetings and training, and coach junior site management staff.
6 Days AgoSaved
Remote
US
Pharmaceutical
Plans and executes B2B marketing campaigns across email, social, paid advertising, content, PR, and internal communications. Creates content, manages vendors and budgets, updates the website, supports digital and in-person events, tracks and optimizes campaign performance, contributes to marketing strategy, and mentors junior team members.
6 Days AgoSaved
Remote
US
Pharmaceutical
Executes B2B digital marketing initiatives across email, social media, lead generation, and nurture campaigns. Monitors and qualifies inbound leads, manages HubSpot workflows and CRM data, coordinates with Business Development, develops campaign content, and analyzes performance metrics. Supports email strategy, reporting dashboards, audience targeting, marketing automation, webinars, conferences, and continuous process improvement.
23 Days AgoSaved
Remote
US
Pharmaceutical
Lead regional delivery of clinical trials across multiple countries, partnering with PMs, CRAs, sponsors and cross-functional teams. Manage planning, KPIs, timelines, site startup/monitoring, regulatory submissions, safety reporting, budgets and team performance while ensuring ICH-GCP and sponsor/QMS compliance. Mentor and train project teams and monitors, prepare study documentation and support audit/inspection readiness.
25 Days AgoSaved
Remote
US
Pharmaceutical
Provide operational support for clinical study startup in the US: site activation, feasibility research, eTMF tracking, site agreements and budgets, IRB/IEC and IP-RED document collection, communication with sites/vendors, progress reporting, and preparation of study dossiers and audit documentation.