Una candidatura hecha para este puesto de trabajo — un currículum y una carta de presentación adaptados que responden directamente a la oferta.
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 years in Clinical Research or CRO with investigator/site contracts, excellent English and local language skills, and proficiency with MS Word,
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 years in Clinical Research or CRO with investigator/site contracts, excellent English and local language skills, and proficiency with MS Word,