Jobs at PSI CRO

Plan, coordinate, and execute international meetings for clinical projects. Manage logistics, vendors, travel, budgets, compliance with HCP interaction rules, registration systems, invoicing, investigator reimbursements, and post‑event follow-up and reporting to finance.

Manage clinical trial data lifecycle: track database setup, design eCRFs, develop data management and validation plans, test EDC, ensure data entry and validation, code medical data, reconcile SAEs, report metrics to database lock, maintain DM documentation, perform QC and audits, and train site staff and project teams.

Plan, coordinate, and execute international investigator and project meetings. Manage logistics, vendors, travel, budgets, invoices, registration systems, compliance with HCP rules, and post‑event follow-up and expense reporting.

Provide administrative support to clinical research projects: maintain databases and tracking systems, manage document processing and translations, coordinate communications with sites and vendors, handle mail/calls, assist meeting logistics, and prepare agendas and minutes. Serve as primary contact for site query resolution, training, and system access.

Provide operational support for clinical study startup in Türkiye: site identification, regulatory/ethics documentation, site contracts and budgets, communication with stakeholders, monitoring startup timelines and metrics, and driving process improvements until site activation.

Provide site-level support for clinical trials: primary contact for sites and vendors, manage supplies, regulatory submissions, TMF/ISF, CTMS/EDC tasks, training coordination, and document management ensuring safety information flow.

Provide administrative support for clinical research projects: maintain databases and tracking systems; act as primary contact for sites, vendors, and study supplies; manage documents, mail, payments, meeting arrangements, and minutes; coordinate site queries, training, and vendor system access; communicate with internal departments and external stakeholders.

Provide legal support focused on clinical research contracts: review, draft and negotiate agreements with medical institutions, suppliers and partners; advise internal teams; ensure policy compliance; research legal issues and support regional legal matters.

Provide administrative support for clinical research: maintain databases and tracking systems, manage and file documents, coordinate site communications, assist meeting logistics, and prepare agendas and minutes.

The Grants Expense Coordinator ensures timely payments for physicians and hospitals involved in clinical trials, handling budgets and payment calculations while coordinating across teams.

Provide administrative and site-facing support for clinical trials, including vendor and supplies coordination, regulatory and TMF document preparation and checks, site payments and training coordination, audit support, and basic coaching of junior site staff.

Lead US business development for a CRO: prospect and win new accounts, build executive relationships, develop account-specific sales strategies and proposals, lead pitches, coordinate with Operations and Proposal teams, negotiate contracts and scope changes, ensure smooth hand-off to project teams, monitor customer satisfaction, and represent the company at industry events.

Coordinate non-participant site operations, manage regulatory and trial documentation (TMF/ISF), support site payments, audits, EDC completion tracking, training, and internal communications. Serve as main administrative site contact and coach junior site staff.

Facilitate negotiation and execution of clinical trial site agreements and budgets, customize and track site-specific contracts, coordinate signatures and translations, file executed agreements in the Trial Master File, and update stakeholders on contracting status.

Manage the feasibility process, evaluate clinical sites, develop patient recruitment strategies, and ensure compliance with timelines and quality standards.

The Coordinator of Project Expense Management is responsible for verifying expense reports, ensuring compliance, producing accrual reports, and performing administrative tasks.

Provide supervised daily IT support and troubleshooting for desktop systems and peripherals; handle ticketing, asset management, installations, configurations, documentation, and basic user training under team supervision.

Provide administrative support for clinical research projects: maintain databases and tracking systems, manage documents, coordinate site and vendor communication, assist with meetings, manage payments, and prepare agendas and minutes.

The Site Coordinator facilitates communication between sponsors and clinical sites, oversees monitoring visits, tracks patient enrollment, and manages documentation according to protocols.

Identify, qualify, and onboard medical institutions into a clinical site network; conduct outreach and introductory meetings; build sponsor/CRO and site relationships; support trial identification, site profiling, and implementation; coordinate documentation and provide business development support to place clinical trials.