Jobs at PSI CRO

Lead and deliver statistical activities for global clinical trials: design and conduct interim/final/DSMB and PK analyses, develop and review protocols, SAPs and ADaM datasets, manage statistical deliverables, train staff, support audits, liaise with data management, and act as biostatistics project lead and client-facing statistical contact.

Lead and perform statistical activities for global clinical trials, including interim/final/DSMB and PK analyses. Develop and review protocols, SAPs, ADaM dataset specs, and deliverables. Lead project teams, provide training, support audits, liaise with data management, and contribute to quality systems and bid/kick-off meetings.

Provide operational support for UK clinical study startup, manage site activation activities, compile and file TMF and IP-RED packages, coordinate site agreements/budgets, oversee investigational product distribution, and develop site-specific startup timelines.

Manage end-to-end oversight of clinical trial committees (IDMC, Safety, Adjudication), coordinating meetings, member selection, charters, FMV assessments, documentation, audits, and stakeholder communications to ensure compliant, high-quality committee governance across studies.

Manage end-to-end clinical trial committee activities (IDMC, Safety Review, Adjudication), coordinate meetings and communications, develop charters and documentation, select and engage external experts, perform Fair Market Value assessments, support audits/inspections, and improve committee processes and training to ensure compliant, high-quality oversight throughout the clinical trial lifecycle.

Manage end-to-end clinical trial committee activities (IDMC, Safety Review, Adjudication), coordinate meetings and members, maintain charters and documentation, perform FMV assessments, support audits/inspections, and drive process and training improvements across global project teams.

Manage end-to-end clinical trial committees including setup, member selection, meeting coordination, charter and documentation development, FMV assessments, audit support, training, and stakeholder communication to ensure compliant, high-quality oversight throughout the trial lifecycle.

Manage end-to-end clinical trial committees (IDMC, Safety, Adjudication): setup, member selection, meetings, charters, FMV/honoraria, audits, and training to ensure compliant, high-quality oversight.

Provide administrative support for clinical research projects: maintain databases and tracking systems, manage documents and filings, serve as primary site contact for vendors and supplies, coordinate site communications, training, query resolution, payments, meeting arrangements, and drafting agendas/minutes. Requires a Life Sciences degree and business-level Japanese (JLPT N2), plus Thai and English language ability.

Lead country-level study activation and support clinical research teams to ensure timely site activation. Maintain startup tracking systems, facilitate budgets and contracts, support regulatory document collection and submissions, manage site timelines and TMF maintenance, communicate with project teams and sites, and assist with translations as needed.

Develop and maintain relationships with clinical investigators and healthcare organizations to identify, onboard, and support qualified clinical research sites. Represent the company at meetings and events, evaluate site capabilities, collaborate with internal teams to support business development, and ensure ongoing site engagement and satisfaction.

Lead Project Manager oversees small-to-medium international clinical trials, ensuring deliverables meet quality standards, timelines, and budgets. Co-manages complex programs, provides project team leadership, mentors and trains staff, participates in feasibility and business development activities, and implements company practices and compliance.

Lead and deliver medium-to-large global clinical projects, ensuring on-time, on-budget, high-quality deliverables. Manage project teams, vendors, client escalation, mentor regional leads, support feasibility and business development, and enforce company standards and compliance.

Lead full-cycle recruitment for US and Canada: source, screen, interview, present offers, run background checks, maintain ATS candidate databases, develop job ads, build talent pipelines, liaise with hiring managers and agencies, report analytics, and improve recruiting processes while promoting the employer brand.

Lead full-cycle recruitment for US and Canada roles: source candidates, post ads, screen resumes, conduct first-stage interviews, manage ATS, build talent pipelines, liaise with hiring managers and agencies, run background checks, report metrics, promote employer brand, and improve recruiting processes.

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.

The Study Startup Manager leads startup operations across 1 to 3 countries, ensures compliance, and oversees team training and quality assurance initiatives.

The intern provides administrative support for the Study Startup department, assists with feasibility research, and maintains tracking systems and electronic files during the startup phase.

Lead and execute B2B marketing campaigns across email, social, paid ads, content and PR; create content; track and optimize campaign performance; manage vendors, budgets, website updates, and events; support sales initiatives and contribute to marketing strategy while mentoring junior team members.

Lead country-level study activation by coordinating site activation, agreements, contract and budget negotiations, IRB/IEC and authority submissions, translations, IP distribution, site documentation exchange, and timelines to meet site activation targets.