Aidez-nous protger Glassdoor en confirmant que vous tes une personne relle. . Theres also regular training with my supporting managers, who I can discuss my ambitions with and together we work on goals I want to achieve. . Caso continue recebendo esta mensagem, When youre travelling between sites and have a period of time away from home, its important to plan in advance to ensure you can see friends and family and visit the places youd like to go. Senior Project Manager 18 days ago Typically, a clinical research career path begins with a degree in life sciences or a related field. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients lives. These numbers represent the median, which is the midpoint of the ranges from our proprietary Total Pay Estimate model and based on salaries collected from our users. enva un correo electrnico a Study Start-Up Associate salaries at ICON can range from $61,563-$74,738. scusiamo se questo pu causarti degli inconvenienti. I appreciate their genius and out-going, down-to-earth nature. The estimated total pay for a Study Start-up is $140,592 per year in the United States area, with an average salary of $125,851 per year. envie um e-mail para Ci Thats why we have developed additional learning opportunities & training programmes for continued growth in various career paths. . Ci Our diverse teams enable us to become a better partner to our customers and help us to fulfil our miss, Our people are our greatest strength, are the core of our culture and the driving force behind our success. If youre just starting your clinical research career and need help navigating your options, we can help. ICON offers a broad range of specialised services to assist pharmaceutical, biotechnology and medical device companies to bring new drugs and devices to market faster. The Role To review and negotiate clinical site investigator contracts and budgets. Stay connected with Investigative sites, sponsors and internal personnel regarding the status of contracts and contract-related documents Prepare and coordinate preparation of contractual documents and correspondence Facilitate the indemnification process between the study sponsor and the site. Function as the internal consultant on study budgets (investigator payments, develop and update training documentation and conduct group training as necessary, mentor and train new and junior personnel in the SSU department, and act as consultant on the Investigator Contract and Budget development process from origination through execution).What you need A bachelors degree in Paralegal Studies, Juris Doctor (law) degree, or related experience is preferred SSU experience is desirable but not required. Experience in a clinical research environment with specific experience in study contracts review and budget negotiation or in related field such as where contract or legal document review is a primary part of you role.Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. They work closely together with our customers to tackle complex issues that can improve the health of patients and the care they receive. Onze 100% Remote Job Full-Time Employee US National 7+ years' relevant work experience with a focus on clinical data management, 4+ years as a Trial Data Manager with full accountability across study startup, conduct, and lock. para informarnos de que tienes problemas. The people at ICON! Aydanos a proteger Glassdoor y demustranos que eres una persona real. om ons te informeren over dit probleem.

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