Assisting in the design of clinical trials and development of study protocols that outline the objectives, methodology, participant eligibility criteria, and endpoints of the trial.

Providing expertise in regulatory requirements and obtaining necessary approvals from regulatory authorities for conducting clinical trials.

Identifying and selecting appropriate clinical trial sites, managing site initiation visits, providing training to site staff, and overseeing site activities
throughout the trial.

Conducting regular monitoring visits to clinical trial sites to ensure adherence to protocol, Good Clinical Practice (GCP) guidelines, and regulatory requirements.

Collecting, managing, and analyzing clinical trial data, ensuring data accuracy, integrity, and confidentiality.

Monitoring and reporting adverse events and safety data throughout the duration of the trial, and ensuring compliance with safety reporting requirements.

Conducting quality assurance activities and audits to ensure compliance with regulatory requirements, protocol adherence, and data integrity.

Overseeing all aspects of the clinical trial, including timelines, budgets, and resource allocation, to ensure timely and successful completion of the study.

Preparing clinical study reports, regulatory submissions, and other documentation required for regulatory approval and publication of trial results.

Planning and execution of research and continuing medical education (CME) programmes, contributing to existing scientific evidence, expert advisory board members, enhancing knowledge and best practices.