Associate Director Clinical Data Management, Oncology

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and...

**Clinical Research Associate - World Leading CRO - Permanent** We are seeking an experienced Clinical Research Associate to take on an exciting opportunity with an international CRO that is continuing to lead from the front in the industry. Utilising their unique experience and global reach, this CRO has regularly demonstrated why they are market leaders...

Proclinical are partnering with a biotech organisation who are recruiting for an individual to join their team. This role is on a permanent basis with the ability to work remotely from anywhere in Germany. The opening position that is currently available is for an Associate Director Statistical Programming. **Responsibilities**: - Assist with the...

Proclinical are partnering with a biotech organisation who are recruiting for an individual to join their team. This role is on a permanent basis with the ability to work remotely from anywhere in Germany. The opening position that is currently available is for an Associate Director Statistical Programming. Responsibilities:Assist with the development and...

Job Overview The Vice President Medical Strategy and Head of the Hematology/Oncology COE provides strategic medical and scientific leadership, subject matter experience and expertise to IQVIA and to IQVIA’s clients in Hematology and Oncology. The overarching remit is to grow IQVIA’s market share in hematology and oncology and will develop strategies...

Title: Global Clinical Operations Manager Location: Remote anywhere in Germany (with travel)✉️ Contact: frankie@elemed.eu The companyHere is a rare and great opportunity to join an international manufacturer in surgical devices and be part of this company’s new digitalized Clinical & Medical Affairs processes. You will be reporting directly to...

Hobson Prior are seeking for a Clinical Research Coordinator to join a fantastic CRO on a contract basis located in Frankfurt. Our client is focused on maximising the speed and effectiveness of the people who conduct clinical trials. Please note that to be considered for this role you must have the right to work in this location. **Key...

**Location**: Frankfurt, Germany or London, UK, with the flexibility to work from home regularly **Duration**: Permanent **Salary**: Competitive, plus benefits **Hours**: 40 per week **About the role**: **Reports to**: Director, Investor Relationships The Associate Director of Investor Relationships will contribute to International Sustainability Standards...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific...

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. Joining the sponsor-dedicated team provides the opportunity to work with early phase clinical research projects (phase I and IIa) in different therapeutic areas.   As...

**The Role**: We are looking for a high-performing and initiative-taking Associate/Senior Associate Director with exquisite corporate comms experience, who will be responsible for managing large client projects, leading cross-border activities, delivering client-ready materials and reviewing the work product of junior team members. You can be based at either...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific...

Overview: The Senior Safety Specialist is responsible for ensuring accurate collection, database entry, review, and reporting of clinical trial and post-marketing safety data. They will be required to assist senior staff in signal generation, safety analysis activities, and to be proactive in the development and implementation of departmental processes and...

Job Description The Opportunity: Embry-Riddle Aeronautical University - Worldwide is seeking an Associate Campus Director (AsCD) to support the Europe Campus location in Frankfurt am Main, Germany. This role participates in student services and the general administrative responsibilities of the campus. Essential Job Functions, Duties, or...

Unternehmensbeschreibung Turner & Townsend zählt zu den führenden, globalen Projektmanagement- und Bauberatungsunternehmen. Mit einem internationalen Netzwerk aus über Mitarbeiter:innen in 48 Ländern unterstützen wir private und öffentliche Bauherren und Investoren bei der Steuerung und Realisierung komplexer Bauprojekte und zukunftsorientierter...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to...

**The Position**: Join our IT EDS Master Data Platform Services - Customer Engagement team as a Senior System Engineer/ Solution Architect. We are a forward-thinking team, always designing new and innovative systems in Master Data Management. In this role, you will be a key player in shaping the future of our data management systems. If you are passionate...

Unternehmensbeschreibung Turner & Townsend zählt zu den führenden, globalen Dienstleistungsunternehmen. Mit einem internationalen Netzwerk aus 118 Büros und über Mitarbeitern unterstützen wir private und öffentliche Bauherren und Investoren bei der Steuerung und Realisierung komplexer Bauprojekte und zukunftsorientierter Infrastrukturprojekte....

Our Purpose We work to connect and power an inclusive, digital economy that benefits everyone, everywhere by making transactions safe, simple, smart and accessible. Using secure data and networks, partnerships and passion, our innovations and solutions help individuals, financial institutions, governments and businesses realize their greatest potential. Our...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to...