Medical Monitor - MBBS/ MD qualification - clinical research
This role supports the safe and effective delivery of clinical trials by providing medical expertise and oversight throughout the study lifecycle. You will act as a key point of contact for sites, ethics committees, and internal teams to ensure protocol compliance and patient safety. The position plays an important part in maintaining high standards of clinical data quality and trial integrity within a growing clinical research environment.
Key responsibilities
* You will review study protocols and offer medical input.
* You will respond to queries and clarifications from ethics committees and institutional review boards.
* You will answer medical and protocol-related questions from investigative sites and the project team.
* You will review patient eligibility and assess adverse events and serious adverse events. You will deliver protocol training to site staff, clinical research associates, and investigators.
* You will attend drug safety meetings, independent data monitoring committees, and investigator meetings, participating or presenting as required.
Essential qualifications and experience
* You will hold an MBBS or MD qualification.
* You will have a minimum of three years of experience working in clinical research.
* You will be familiar with clinical trial operations, electronic data capture systems, and data review tools.
* You will demonstrate excellent written and verbal English communication skills. You will show proficiency in using Microsoft Office applications.
* The ability to evaluate, interpret, and synthesise scientific data.
* A customer-oriented approach with strong planning and organising skills.
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