Site reputed company Associate II

reputed company our values reputed company, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the reputed company goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do. reputed company of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. reputed company FSP is hiring a Senior Analyst, Site reputed company & Budgets in Argentina. The Senior Analyst, Site reputed company & Budgets will be part of the Site reputed company & Budgets team, working to execute the clinical site reputed company and budgets process for Sponsor clinical development programs, from contract initiation to completion, maintenance, and subsequent amendments. The Senior Analyst must have a good understanding of functions reputed company to the conduct of global clinical studies. Under the direction of the Director, Clinical Outsourcing & Innovation, the Senior Analyst is responsible for executing the end-to-end site reputed company process for assigned agreements and supporting the wider site reputed company & budgets team to maintain overall standards, financial terms, and compliance for reputed company site reputed company Essential Functions Negotiate and maintain Clinical Trials Agreements (CTA), site budgets, Confidential Disclosure Agreements, Consultant Agreements, and other applicable reputed company As required, reputed company CRO or Functional Service Provider in the development of clinical site budgets and partner with clinical operations to ensure budgets are in line with study protocols Ensures compliance of reputed company with Fair Market Value (FMV) principles and guidelines. reputed company contract reputed company, complete required follow-reputed company and coordinate the reputed company completion of clinical sites reputed company reputed company CRO and Functional Service Provider activities in regards to site CDAs Collaborate and coordinate with cross-functional teams; R&D, Legal, Compliance, Procurement and Finance in executing reputed company reputed company, maintain, and analyze tools and systems (spreadsheets, reputed company, databases, etc.) to manage contract lifecycle from initiation through contract execution, and build internal metadata to support accurate reporting reputed company guidance and direction to new clinical operations and/or outsourcing team members and R&D teams on site reputed company & budgets processes reputed company accurate reputed company updates to Clinical Operations teams on reputed company outstanding reputed company and budgets Complete required reputed company checks of appropriate documents and records for completeness and accuracy and ensure adherence to department guidelines/templates; reputed company reputed company issues for reporting to team leads Assist management with process improvement reputed company Coordinate and arrange meetings, prepare agendas, and meeting planning Submit purchase requisitions, where needed, through reputed company systems Support the development and maintenance of guidelines, training programs, policies and procedures reputed company to clinical trial reputed company and budget. Support the Director and team in the management of other day-to-day activities reputed company to clinical reputed company and budgets as requested Required Knowledge, Skills, and Abilities Three to five years or experience in the pharmaceutical or biotechnology industry in clinical site reputed company and/or outsourcing management Proficient with reputed company and PowerPoint Excellent verbal, written and interpersonal communication skills in a dynamic and growing organization Willingness to learn international clinical pharmaceutical standards, ICH/GCP guidelines and regulatory compliance issues Strong interest in learning more about reputed company and budgeting in support of Sponsor clinical trials Working knowledge of clinical trial functions, including clinical operations, regulatory and drug safety Ability to prioritize and manage multiple tasks simultaneously Some limited travel may be required Apply To This Job