Local Clinical Trial Application Regulatory Manager Ubicación: Buenos Aires, Argentina Permanent, Full time Acerca del rol The Clinical Trial Application Regulatory Manager (CTA-RM) is the responsible person to ensure that the regulatory dossiers related to Clinical studies (New initial CTA, Amendments,
PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services
Local Clinical Trial Application Regulatory Manager page is loaded Local Clinical Trial Application Regulatory Manager Apply locations Buenos Aires Santiago time type Full time posted on Posted Yesterday job requisition...
Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add and established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group...
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to...
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether
PPD is a leading global contract research organization. At PPD we are passionate, deliberate, and driven by our purpose - to improve health. Site and Patient Access is a global department working to provide rapid site
We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD clinical research services — thousands of employees in locations worldwide connected by tenacity and
PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but
Job Overview Under general direction, manage all laboratory aspects of assigned clinical trial projects for a Customer or a specific program for a Customer. May have responsibility for a specific Customer, drug program, indication or drug compound. Acts
Job Overview Responsible for Project Management operational delivery. Serve as key contact for internal/external business relationships. Manage the design/launch of non-standard, complex clinical research studies as assigned. Review processes, to develop, integrate, administer, and maintain current Project
Job Overview Leader of the Centralized Monitoring team, partner with the project and clinical lead to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction per contract, while optimizing speed, quality and cost of
Job Overview Under general direction, manage all laboratory aspects of assigned clinical trial projects for a Customer or a specific program for a Customer. May have responsibility for a specific Customer, drug program, indication or drug compound. Acts
Are you a freelance translator with a passion for life sciences content? Join us on an exciting journey and become a member of our growing global community of linguists. The IQVIA Translation Services team is looking
Come and join our Oncology team! Regarding the role. Senior Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Senior Project
Job Overview Provide support to the Project Manager and related team members by performing routine procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g. start-up, maintenance and
Coordinating CRA (CCRA) PURPOSE OF THE ROLE To take the lead on behalf of the CFSP Clinical Monitoring department, as representative on the Study Team for our function. Responsible for operational management of a team of Monitors
Job Overview Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include
HOW MIGHT YOU DEFY IMAGINATION? You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and...
Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary...
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