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Clinical Trial Coordinator

hace 2 meses

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{"h3": "Clinical Trial Assistant Role Overview", "p": "At Pfizer, we are committed to improving healthcare and transforming lives. As a Clinical Trial Assistant, you will play a vital role in facilitating the conduct of clinical trials and ensuring their progress. Your focus will be on coordinating activities that support the trials and assisting managers in conducting them. Your hard work and dedication will contribute to achieving project tasks and goals, making Pfizer ready to achieve new milestones and help patients across the globe.", "ul": [{"li": "Contribute to the completion of project milestones and organize your work to meet project task deadlines."}, {"li": "Maintain the Pfizer Trial Master File (PTMF) in accordance with International Council for Harmonization - Good Clinical Practice (ICH-GCP) and Standard Operating Procedures (SOPs).", "ul": [{"li": "Review shared spaces to ensure others are updating tracking and files as requested by the team."}, {"li": "Update trial and site information as necessary in the Corporate Clinical Trial Registry in a timely manner."}, {"li": "Support and coordinate the Clinical Trial Application to ethics committees and regulatory authorities, if applicable, to obtain approval within required timelines."}, {"li": "Provide protocol and Informed Consent Document (ICD) administrative support to global Project Managers and Study Managers."}, {"li": "Support and coordinate any activities as requested by PMs/SMs and as assigned within required timelines."}, {"li": "Maintain or develop local tracking spreadsheets for study-related documents, data, activities, and prepare site supportive material."}, {"li": "Attend appropriate training programs and project teleconferences as applicable."}, {"li": "Assist the team with the preparation of any documents or tracking and updating information."}, {"li": "Identify and implement process improvements for inspection readiness, Pfizer Trial Master File (PTMF) compliance, Investigator Meeting organization."}, {"li": "Ensure the reconciliation of Trial Master File and the Site Master File on a periodic basis."}]}, "h3": "Requirements", "ul": [{"li": "Bachelor's Degree"}, {"li": "Relevant work experience in a health-related discipline, pharmaceutical, or medical research"}, {"li": "Demonstrated ability to introduce new ideas"}, {"li": "Knowledge of all relevant Standard Operating Procedures"}, {"li": "Ability to prioritize multiple tasks and develop strategies for the completion of all required activities"}, {"li": "Ability to build collaborative working relationships with colleagues and associates both within and external to the organization"}], "h3": "Nice-to-Have", "ul": [{"li": "Experience in the management of clinical trials and/or regulatory documents"}, {"li": "Knowledge of International Conference on Harmonization Good Clinical Practices and local regulations"}, {"li": "Knowledge of applications used in clinical trials"}, {"li": "Experience with managing site payments"}], "p": "Work Location Assignment: Mexico City (hybrid work model)", "p": "EEO (Equal Employment Opportunity) & Employment Eligibility", "p": "Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.", "h3": "About Us", "p": "Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We're looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place."}