Assist in developing and reviewing the study protocol and associated documents, ensuring they are accurate and adhere to ethical guidelines. Develop clinical trial protocols and objectives. Monitor trial participants and collect data on their reactions to treatments. Oversee data collection, entry, and verification to maintain the integrity of results. Communicate trial progress and findings to stakeholders, including sponsors, regulatory bodies, and other researchers. Prepare detailed reports and scientific papers based on trial outcomes. Coordinate with external vendors, such as laboratories or imaging centers, for any outsourced services needed for the study.

Oversee budgets for clinical trials, ensuring that resources are used efficiently

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Requires a bachelors degree in medicine and at least two years of experience working in the medical field.