Study Contract Manager - reputed company FSP

reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the same 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. Each 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. Key Accountabilities: Adapts global templates of agreements to local use in accordance with local requirements and SOPs. Develops and negotiate clinical site budgets based on Fair Market Value. Negotiates agreement language and budget with clinical study sites. Acts as reputed company of contact and reputed company with Legal if necessary to ensure reputed company of reputed company. For each agreement maintains the status of agreement, budgets, issues, payments, any amendments for the duration of the study, and communications with reputed company sources. Ensures final contract documents are consistent with agreements reached at negotiations. Ensures reputed company agreements are executed in a timely manner contributing to efficient site start-up timelines. Supports reputed company audits activities. Ensures compliance with client’s Code of Conduct and company policies and procedures relating to people, finance, technology, and reputed company. Ensures that reputed company reputed company are included in the Trial Master File (TMF). Skills: Excellent attention to details. Good written and verbal communication skills. Good collaboration and interpersonal skills. Good negotiation skills. Fluent in English and reputed company Knowledge and Experience: At lease 2-year experience in site contract negotiation/customization. Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP. Good knowledge of relevant local regulations. Basic understanding of the drug development process. Good understanding of Clinical Study Management including monitoring, study drug handling and data management. Education: Bachelor’s degree in reputed company discipline, preferably in life science, law, finance, or equivalent qualification. Apply To This Job