The Study Startup Specialist facilitates the study activation process, manages project timelines, and ensures smooth startup communications and documentation for clinical research trials.

Assist in clinical research projects by managing communication, documentation, regulatory submissions, and safety information, while ensuring compliance with audits.

Produce and edit short- and long-form marketing and BD content (blogs, white papers, case studies, website copy). Research topics, interview SMEs, build editorial calendars, and collaborate to ensure brand consistency and measure content performance.

Create and edit marketing and business development content (blogs, white papers, case studies, website copy); research topics and sources; interview SMEs; build editorial calendars; collaborate with marketing to ensure brand consistency and monitor content performance.

Create and edit short- and long-form content (blogs, white papers, case studies, website copy) to support business development and marketing. Research topics, interview SMEs, build editorial calendars, monitor content performance with digital marketing, and ensure consistency with PSI branding and style guide.

Create and edit short- and long-form marketing and business development content (blogs, white papers, case studies, website copy). Research topics, interview SMEs, build editorial calendars, and collaborate with marketing to ensure brand consistency and monitor content performance.

The Full-Stack Developer will create and maintain in-house applications, ensuring adherence to development standards while improving skills and tracking tasks.

As a Data Analyst at PSI, you will collect, prepare, and analyze data to generate insights, validate datasets and create visualizations to support decision-making.

The role involves managing study startup processes for clinical trials, including budget negotiations, document collection, and timeline management.

The Site Identification Specialist develops strategic relationships with clinical research sites, optimizes site identification, and supports clinical trials throughout the startup phase.

The Site Management Associate I supports clinical research projects by managing communications, documents, and supplies, ensuring regulatory compliance, and assisting in audits and team meetings.

Lead and coordinate clinical project teams in Japan, ensuring compliance and achievement of study milestones while managing stakeholder communications.

The HR Associate supports onboarding and offboarding, vendor management, employee queries, and maintains employee files while ensuring compliance with employment laws.

The Marketing Director leads strategic marketing initiatives, mentoring a team, managing campaigns, and enhancing the brand's global presence in the clinical research industry.

The Lead Site Coordinator oversees clinical trial activities at medical institutions, ensuring compliance with protocols and regulations, facilitating communication, supervising staff, and tracking recruitment efforts while supporting training and logistics for successful trial conduct.

The Junior IT Systems Administrator will provide technical support for desktop systems, manage IT operations, and assist with asset management and documentation.

Plan and conduct internal audits across the PSI Group, prepare audit reports, support risk-based audit plans, assess risk management, and improve internal controls in collaboration with stakeholders.

As a Senior Clinical Research Associate, you will conduct monitoring visits, manage site communication, and support regulatory submissions in various therapeutic studies.

The Junior IT Systems Administrator will provide technical support, troubleshoot computer systems, manage assets, document issues, and assist in training staff.

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.