Global Site Contracts Specialist

Who we areWho we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we...

Negotiates and finalizes clinical research contracts remotely for a leading CRO, ensuring compliance with international regulations.

Who We Are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.Who We Are We’re a global, midsize CRO that pushes...

Fortrea Spain S.A. seeks a Site Regulatory & Contract Manager to lead country-level study start-up and regulatory submissions, ensuring trials activate on time and within budget. You will coordinate with Clinical Trial Coordinators, CRAs, regulatory, legal, finance and vendors, manage CTRAs and oversee quality, risk, and timelines across multiple studies in...

Fortrea in Madrid seeks a Site Regulatory & Contract Manager to lead country-level study start-up activities. You will oversee regulatory submissions, approvals, and contract negotiations to initiate trials on schedule. This role requires strong project management, budgeting, and cross-functional coordination with CRAs, regulatory, legal, finance, sites,...

The Site Regulatory & Contract Manager is responsible for leading and overseeing country-level study start-up activities, ensuring clinical trials are initiated on time, within budget, and in compliance with applicable regulations and quality standards. Key Responsibilities Lead country-level regulatory submissions, approvals, and study start-up...

Worldwide Clinical Trials is seeking a Site Contracts professional to manage the drafting, negotiation and finalization of site contracts and related budgets for clinical studies. You will liaise with the Worldwide Legal Department, study teams and regulatory colleagues to ensure compliant, timely execution across multiple sites. The role requires 3–5...

IQVIA Biotech in Madrid, Spain, is seeking a Senior Site Contracts Associate to support start-up contracting for sponsors across Spain, Portugal and Greece, with homebased assignments. You will develop investigator grant estimates, maintain templates, coordinate with sponsors and RSU regions, and ensure compliance with GCP/ICH and regulatory standards. A...

Sulzer, a leading engineering company, invites applications for a Billing Administrator in Madrid (Rivas). This role ensures accurate invoicing, contract administration, and precise customer documentation to support revenue recognition. You will work with Sales and internal teams to maintain efficient billing processes. The ideal candidate has strong...