Job Summary Location: Spain and Hungary Functional Goal: Responsible for the strategic and tactical operational planning and execution of R&D sponsored clinical programs for all corporate sponsored programs for Phase I - Phase IV. Main Tasks: Responsible and accountable for planning, coordinating, overseeing, and conducting complex global clinical trials in one or more therapeutic areas. Collaborate in a global environment, using best practices and knowledge of internal and external business issues to improve processes, standards, and services. Accountable to plan, drive and monitor protocol related activities throughout the lifecycle of the project ensuring targets are met according to timelines, budget and quality expectations. Lead (multiple) cross-functional teams and drive oversight of CRO’s and vendor management and has in-depth business knowledge and strategic understanding of how cross-functional teams jointly achieve objectives and goals of trial team, utilizing knowledge of the organization, processes, customers, and key business drivers to increase effectiveness. Understand the different requirements of agencies related to the clinical packages and plans manages accordingly the different functions (i.e. CSR, TFLs, ISS etc.) Responsible for inspection readiness. Accountable for CAPAS related to clinical programs within the field of Clinical Operations. Accountable and responsible for the financial planning, budget, accruals, forecasts contribution. Preparing clinical program updates and/or contribution to them as needed. Qualification profile: Advance degree in life sciences (graduate degree), e.g. Biology, Chemistry, Pharmaceuticals preferred or medical background At least 7 years’ experience in clinical research in industry, and at least 5 years in clinical trial management Understanding GxP and global requirements Strong project management skillsets Excellent communication skills and ability to manage cross functional teams Ability to deal with complex situations and drive solution orientated thinking Fluent in English Excellent team player, ability to work under high pressure and pronounced resiliency Experience working in an international and cross-functional team Ability to present and defend the perspective Experienced in Microsoft project, Excel, Power point Other Tasks: Participate in relevant meetings Plan and set up cross-functional meetings, meetings with vendors and others as needed Own and/or contribute to SOP development /reviews Support sponsor oversight through participation in site visits, including Site Initiation Visits (SIVs) and Co-Monitoring Visits, as required Regular Fresenius Kabi (www.fresenius-kabi.com) is a global health care company that specializes in injectable medicines, biosimilars, and technologies for infusion, transfusion, and clinical nutrition. Our expansive portfolio of products and global network of science and manufacturing centers provide essential support for the care of critical and chronically ill patients. With more than 40,000 employees working in 60 countries, our dedicated team is united by our shared purpose: to put lifesaving medicines and technologies in the hands of people who care for patients - and to find answers to the challenges they face. We call this purpose committed to life. We are proud to be part of the Fresenius Group with its more than 190,000 employees worldwide. Everyday, we use our dedication, expertise, and passion to help advance healthcare opportunities and make a difference in people’s lives everywhere. Follow us on Linkedin to learn more.

Senior Manager Clinical Operations (m/f/d).

more at Freseniusglobal.

Senior Manager Regulatory Affairs Lead

Senior Manager European Patent Attorney (m/f/d)

Internship Marketing

similar roles.

QC Inspector

Operator Shift B

Case Management Specialist - Generalist

Case Management Specialist - Generalist

Facilitadores de Sociedad I

Especialista em Inovação e Novos Modelos Programáticos II