.We're in relentless pursuit of breakthroughs that change patients' lives. We innovate every day to make the world a healthier place.To fully realize Pfizer's purpose – Breakthroughs that change patients' lives – we have established a clear set of expectations regarding "what" we need to achieve for patients and "how" we will go about achieving those goals.Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple: empower healthcare decisions regarding the safe and appropriate use of medicines for patients.What You Will AchieveYou will facilitate in conducting clinical trials and monitoring their progress. You will coordinate all activities that support the clinical trials and assist the managers in conducting them. As an associate, your focus on the job will contribute to achieving project tasks and goals.It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.How You Will Achieve ItContribute to completion of project milestones and organize own work to meet project task deadlines.Maintain Pfizer Trial Master File (PTMF) in accordance with International Council for Harmonization - Good Clinical Practice (ICH-GCP) and Standard Operating Procedures (SOPs).Review shared space to ensure others are updating tracking and files as requested by the team.Update the trial and site information as necessary in Corporate Clinical Trial Registry in a timely manner.Support and coordinate the Clinical Trial Application to ethics committee and regulatory authority, if applicable, to obtain approval within required timeline.Provide protocol and Informed Consent Document (ICD) Administrative Support to global Project Managers and Study Managers.Support and coordinate any activities as requested by PMs/SMs and as assigned within required timelines.Maintain/develop local tracking spreadsheets for study-related documents, data, activities and prepare site supportive material.Attend appropriate training programs and project teleconferences as applicable.Assist team with the preparation of any documents or tracking and updating information.Identify and implement process improvements for inspection readiness, Pfizer Trial Master File (PTMF) compliance, Investigator Meeting organization
