Fsp - Sr. Regulatory And Start Up Specialist In Brazil

Detalhes da Vaga

Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and contractual/budgetary guidelines.
May also include maintenance activities.Essential Functions• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.
Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables, and project timelines.• Perform start-up and site activation activities according to applicable regulations, SOPs, and work instructions.
Distribute completed documents to sites and internal project team members.• Prepare site regulatory documents, reviewing for completeness and accuracy.• Ensure accurate completion and maintenance of internal systems, databases, and tracking tools with project-specific information.• Review and provide feedback to management on site performance metrics.• Review, establish, and agree on project planning and project timelines.
Ensure monitoring measures are in place and implement contingency plans as needed.• Inform team members of completion of regulatory and contractual documents for individual sites.• Review, track, and follow up on the progress, approval, and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.• Provide local expertise to SAMs and project team during initial and ongoing project timeline planning.• Perform quality control of documents provided by sites.• May have direct contact with sponsors on specific initiatives.Qualifications Needed• Bachelor's degree in Health Sciences.• +2 years of experience in the Site Activation/Regulatory department in:ICF customizationPreparation and submission of studies in startups to local and central ethics committeesCollection of essential documents from the sitesPreparation of initial DEEC for ANVISAExperience in annual and final study reports• Advanced level of English.• Excel knowledge.This is a home-based position!
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Salário Nominal: A acordar

Fonte: Whatjobs_Ppc

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