The IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client’s project team to set-up and execute clinical trials. As Clinical Trial Leader (m/w/d) you will be accountable for the operational performance
Company Description PSI is a global Contract Research Organization (CRO) with over 30 years of experience supporting clinical research around the world. We combine the stability of an established organization with the agility and innovation needed
This is Readly / Cafeyn Readly offers unlimited access to thousands of national and international magazines and newspapers, all in one app. We’ve partnered with 1,200+ world-famous publishers, providing readers with 5,000+ titles and over 290,000
This is Readly / Cafeyn Readly offers unlimited access to thousands of national and international magazines and newspapers, all in one app. We’ve partnered with 1,200+ world-famous publishers, providing readers with 5,000+ titles and over 290,000
Project Manager / Clinical Trial Lead - sponsor dedicated - Germany Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development
Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice
Senior CRA - Phase I oncology trials - Hamburg/Berlin region Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and
IQVIA Clinical Functional Service Partnerships (Clinical FSP) department is providing highly skilled professionals to our client’s project team to set-up and execute clinical trials. Site Management Lead is a key member of global Clinical Trial Team nominated to a
Your responsibilities will include Assessing data sharing requests, reviewing informed consent forms for data sharing feasibility Redaction of clinical trial documents and anonymisation of individual patient data Preparing Redaction Proposal Document Packages (RPDP) for submission to EMA
Mainz, Germany | full time | Job ID: 9134 BioNTech SE is seeking an insurance professional with a strong legal background to support and further develop our global liability insurance portfolio. While the role has a
Description The Project Manager II, EPTR has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The Project Manager II, EPTR oversees and coordinates study resources to ensure compliance
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
APM Terminals At APM Terminals, a global leader in port and terminal operations, we enable global trade and drive sustainable growth. What drives us forward is a mindset of always improving — observing how work happens,
APM Terminals At APM Terminals, a global leader in port and terminal operations, we enable global trade and drive sustainable growth. What drives us forward is a mindset of always improving — observing how work happens,
Your Talent, our Vision – together we see beyond. Your start at ZEISS Vision Care. As a leading manufacturer of ophthalmic lenses, we help people around the world achieve a clearer vision – sustainable and with
Munich, Germany; London, United Kingdom; Mainz, Germany | full time | Job ID: 11648 About the Role As a (Senior) Director of Clinical Development at BioNTech, you will collaborate closely with the VP of Clinical Development
Munich, Germany | full time | Job ID: 11640 As a Project Manager in the CMC Project Management Team at BioNTech, you will be part of cross-functional project teams in a variety of late phase CMC development
Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join
The Position We at Boehringer Ingelheim Medicine share one vision: to turn patient-focused innovations into life-changing treatments. We focus on driving medical innovation, combining scientific and patient insights to develop and deliver safe and effective solutions.