Clinical Research Coordinator

hace 4 semanas


Xico, México Pfizer A tiempo completo
Empowering Healthcare Decisions

Pfizer Worldwide Medical and Safety colleagues play a pivotal role in connecting evidence-based medical decision support with colleagues and stakeholders to drive better health and treatment outcomes. Our mission is to empower healthcare decisions regarding the safe and appropriate use of medicines for patients.

Key Responsibilities
  • Facilitate the conduct of clinical trials and monitor their progress.
  • Coordinate all activities that support clinical trials and assist managers in conducting them.
  • Contribute to the completion of project milestones and organize work to meet project task deadlines.
  • Maintain the Pfizer Trial Master File (PTMF) in accordance with International Council for Harmonization - Good Clinical Practice (ICH-GCP) and Standard Operating Procedures (SOPs).
  • Review shared spaces to ensure others are updating tracking and files as requested by the team.
  • Update trial and site information as necessary in the Corporate Clinical Trial Registry in a timely manner.
  • Support and coordinate the Clinical Trial Application to ethics committees and regulatory authorities, if applicable, to obtain approval within required timelines.
  • Provide protocol and Informed Consent Document (ICD) administrative support to global Project Managers and Study Managers.
  • Support and coordinate activities as requested by PMs/SMs and as assigned within required timelines.
  • Maintain or 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 the 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.
  • Ensure the reconciliation of Trial Master File and the Site Master File on a periodic basis.
Requirements
  • Bachelor's Degree
  • Relevant work experience in a health-related discipline, pharmaceutical, or medical research
  • Demonstrated ability to introduce new ideas
  • Knowledge of all relevant Standard Operating Procedures
  • Ability to prioritize multiple tasks and develop strategies for completion of all required activities
  • Ability to build collaborative working relationships with colleagues and associates both within and external to the organization
Work Location Assignment

Mexico City (hybrid work model)

EEO (Equal Employment Opportunity) & Employment Eligibility

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.



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