Heather Mcdonald Email & Phone Number

As a Site Monitor at Discovery Life Sciences, I oversee the progress of clinical studies, both on-site and remotely, and ensure they are conducted, recorded, and reported in accordance with site protocols, SOPs, ICH-GCP, and regulatory requirements. I have years of experience in clinical trial management, spanning multiple therapeutic fields and phases of research.I am passionate about supporting clinical research through enhanced study oversight and quality control, and I collaborate with internal and external stakeholders to execute processes for maximum effectiveness and performance. I also contribute to the development and maintenance of tracking tools, web portals, training materials, and metric reports. I will be graduating with a dual focus master's degree in clinical research management & regulatory science. I also have several certifications in relevant skills, such as data analysis, communication, and feedback. Additionally, I have published research on the Latretium phage virus as a contributing researcher.

Listed skills include Career Management, Clinical Trials, Career Path Planning, Informed Consent, and 46 others.