
10,000+ employees
Founded 1983
âïž Healthcare Insurance
đ§Ź Biotechnology
đ Pharmaceuticals
đ° Venture Round on 1990-01
Healthcare Insurance âą Biotechnology âą Pharmaceuticals
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
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10,000+ employees
Founded 1983
âïž Healthcare Insurance
đ§Ź Biotechnology
đ Pharmaceuticals
đ° Venture Round on 1990-01
Healthcare Insurance âą Biotechnology âą Pharmaceuticals
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
âą Responsible for negotiation with sites, finalization, and execution of all types of site contracts required for site activation including budget negotiations âą Manage the negotiation, finalization, and execution of any amendments to the original contracts post site activation âą Ensure the highest standard of quality of final documents and compliance with relevant regulatory requirements including ICH â GCP âą Ensure that contracts meet needs of both clients and clinical trial sites, protecting best interests of clients and the company while nurturing positive relationships with clinical trial sites
âą 2 to 5 years of experience in clinical research site contracts support or related field âą Experience negotiating, reviewing, and managing legal, commercial, or clinical trial-related agreements âą Experience working with contract language, budgets, and financial terms âą Strong analytical skills with the ability to interpret legal language and budget information âą Excellent negotiation, organizational, interpersonal, and communication skills âą Demonstrated ability to manage multiple projects and priorities in a fast-paced environment âą Strong attention to detail and commitment to quality âą Fluent written and spoken English âą University degree in a related field; candidates with a degree in Law are highly relevant âą Conversational Portuguese is a plus but not mandatory.
âą N/A
Apply Nowđ July 8
Deal Desk Associate supporting operational execution and strategic responsibilities in a global SaaS company. Contributing to order management and process improvements within a flexible and remote team.
đŠđ· Argentina â Remote
đ” $24.6k - $55.3k / year
â° Full Time
đą Junior
đĄ Mid-level
âš Associate
đ«đšâđ No degree required
đ June 19
Support management of clinical trial sites ensuring compliance with study protocols. Collaborate with cross-functional teams and maintain operational efficiency in clinical research.