Amina Dockery

Background

About Amina Dockery

I am a seasoned Clinical Trial Manager with nearly 20 years of report monitory and process development experience in the pharmaceuticals sector. Recognized for demonstrating a natural aptitude for ensuring regulatory compliance, as well as for optimizing process flows and conducting effective quality control reviews, I have a verifiable history of contributing directly to company growth and expansion throughout my career. As such, I have consistently exceeded performance goals and I am adept at leveraging cross-functional collaboration and seamless operations to achieve desired results. Professional focal points include timely task execution, efficient organization, multi-task prioritization, team collaboration, and interpersonal communication. Delivering superior administration on the latter areas of expertise requires utilization of effective communication skills, analytical skills, as well as industry acumen, systems analysis, project management and resource management to support efficiency and maximum returns. Currently, I am the Clinical Trial Manager II with Alexion Pharmaceuticals. Under my leadership, I ensure quality of Trial Master files by conducting quality content (QC) review of document packages submitted for entry into the TMF and collaborating with project teams to identify and resolve any issues. I also monitor update of registration of a protocol in ClinTrials.gov/EUdract throughout various studies’ life cycle to ensure compliance with regulations and SOP. In addition, I directly assist CPL with CRO interactions, as well as with ensuring and enforcing compliance to all study level plans, industry regulations, and SOP. I am pursuing new opportunities and can be reached through this profile, or by email at amina.dockery@yahoo.com.