Site Contract Specialist

Há 12 horas

São Paulo, Brasil Alimentiv Tempo inteiro

Get AI-powered advice on this job and more exclusive features. The Site Contract Specialist will be responsible for the execution, negotiation and administration of assigned site contracts and supporting documents including confidentiality agreements, clinical trial agreements, letters of indemnity and authorization. The incumbent will coordinate with sites, sponsors, vendors and internal stakeholders to facilitate the timely execution of contracts in accordance with project, corporate, industry and regulatory best practices and guidelines. Provide training on internal site contract processes and some mentoring of department staff. Support the department and company in achieving objectives and strategic goals. Site Contract Management and Execution Coordinate the review and negotiation of new site contracts and amendments and secure the approvals from internal stakeholders, sponsors, and clinical trial sites, required for the execution of contracts and supporting documents on a timely basis. Ensure all work and final documents align with SOPs and project protocols, corporate, industry and regulatory standards and legal best practices. Engage the services/guidance of outside legal counsel as required. Ongoing Site Contract Process Development Support Manager, Contracts & Compliance in developing site contracting processes and policies. Assist Manager, Contracts & Compliance in the creation and ongoing maintenance of site agreement templates. Act as an escalation point for Contract Coordinators for legal or process questions arising in site contracts. Corporate Contract Services Support Provide support to the Legal team in the review and execution of corporate contracts including project orders, change orders and confidentiality agreements, particularly those related to full-service projects. Qualifications Minimum experience: 1-3 years of related experience, post-secondary certificate/diploma (College, Training Institute, etc.). Preferred experience: 4-6 years of related experience, (Honors) bachelor’s degree. Language requirements: High level of fluency in written English to facilitate contract negotiations; Knowledge of other languages (e.g. Polish, Hungarian, Spanish, French, Italian) is an asset. Additional Knowledge/Skills Preferred legal-related diploma, degree, designation or paralegal certificate. Contract management and negotiation experience is required, preferably within the pharmaceutical, biotechnology, or contract research organization (CRO) industry. Experience with clinical trial agreements and site contracts preferred. Working Conditions Home based. Accommodations for job applicants with disabilities are available upon request. Accommodations for persons with disabilities are available on request in respect of all aspects of the recruitment and selection lifecycle. Requests can be directed to #J-18808-Ljbffr

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