Work Schedule Standard Mon-Fri Environmental Conditions Office RCR Specialist Admin Regulatory Compliance Review Regulatory Affairs Perform global regulatory compliance review of essential documents supporting the customization of study-specific Essential Document Checklists Respond to project teams on queries on Essential Document Checklist requirements Where required applicable facilitate discussion of requirement of deviation to the RCR process with the project teams Ensure effective management and coordination of the Essential Document Checklist Process Maintain knowledge and understanding of PPD SOPs Client SOPs directives and current regulatory guidelines as applicable to services provided Responsible for reviewing finalizing and posting of the Essential Document Checklists Other duties as required Qualifications Education and Experience Bachelor s degree or equivalent and relevant formal academic vocational qualification Previous experience that provides the knowledge skills and abilities to perform the job comparable to 1 to 3 years Knowledge Skills and Abilities Good English language written and oral communication skills as well as local language where applicable Good attention to detail and quality as well as editorial proofreading skills Good interpersonal skills to work effectively in a team environment Good computer skills including the use of Microsoft Word Excel Power Point capable of learning new technologies Basic organizational time management and planning skills to create and follow timelines conduct long-range planning adapt to changing priorities and handle multiple projects Basic knowledge of global regional national country requirements regulatory affairs procedures for clinical trial authorization licensing lifecycle management Valuable analytical investigative and problem-solving skills Capable of interpreting data