Data Management Leadership Position for Oncology Trials

Job SummaryWe are seeking an experienced Oncology Trial Data Manager to join our team at Fortrea. The successful candidate will have a strong background in clinical data management and experience leading studies in a CRO/Pharma setting.This role offers an exciting opportunity for a skilled professional to take ownership of data management for oncology trials...

About the RoleWe are seeking a seasoned Clinical Data Management expert to lead complex oncology clinical trials. As a Senior Clinical Data Manager, you will oversee the full cycle of CDM queries, from leadership to hands-on tasks.Job SummaryThe successful candidate will be responsible for:Leveraging expertise in leading complex oncology clinical trials and...

We are seeking a highly experienced Clinical Data Management Leader to join our team in EMEA. This role is responsible for providing leadership and operational expertise in the strategic planning and delivery of Clinical Data Management (CDM) deliverables at program and/or project level.Key Responsibilities:Provide CDM leadership for one or more assigned...

Unlock a Rewarding Career in Oncology Clinical TrialsWe are seeking an exceptional Senior Clinical Data Manager to join our team at Lifelancer, a leading talent-hiring platform in Life Sciences and Pharma. As a key member of our organization, you will play a vital role in the delivery of complex oncology clinical trials.About the Role:This is a fantastic...

About the RoleAs a Senior Statistical SAS Programmer in our Oncology team, you will play a crucial role in the successful delivery of complex clinical trials for renowned pharmaceutical companies.You will be responsible for developing and validating SAS programs for data presentations and analyses, and providing programming support to your global project...

About the RoleWe are seeking an experienced Statistical Programmer to join our team in a Senior role. In this position, you will be responsible for developing and validating SAS programs for data presentations and analyses, as well as providing programming support to your global project team.This is an excellent opportunity to participate in the development...

Senior Statistical SAS Programmer RoleLifelancer, a talent-hiring platform in Life Sciences and IT, is seeking an experienced Senior Statistical SAS Programmer to join our team. As a key member of our Flexible Solutions business unit, you will be responsible for delivering high-quality clinical trials (phases I-III) for top pharmaceutical companies.About the...

Job OverviewFortrea is seeking an experienced Clinical Trials Data Specialist to join our sponsor-dedicated Flexible Solutions business unit. As a key member of our global project team, you will be responsible for developing and validating SAS programs for data presentations and analyses.The ideal candidate will have a strong background in statistical...

About the RoleWe are seeking a highly experienced Clinical Data Management Lead to join our team at Fortrea, a global contract research organization. This is an excellent opportunity for a skilled professional to lead complex oncology clinical trials and contribute to the development of life-changing therapies.The successful candidate will have extensive...

Director of Oncology Medical AffairsAt AbbVie, we are seeking a highly skilled Director of Oncology Medical Affairs to lead our UK Oncology Medical Affairs Department. This is a critical leadership role that requires a strong background in oncology, experience in managing complex teams, and a deep understanding of the pharmaceutical industry.Key...

Job SummaryFortrea is seeking a highly skilled Senior Clinical Data Manager to join our team in EMEA. As a Senior Clinical Data Manager, you will be responsible for leading complex oncology clinical trials and providing CDM leadership for one or more assigned projects or indications. You will demonstrate leadership and operational expertise in the strategic...

Data Management Leadership Opportunity at FortreaFortrea, a leading global contract research organization, is seeking a Senior Clinical Data Manager to join our team. As a Senior Clinical Data Manager, you will play a key role in the drug development cycle, overseeing the management of clinical data on large-scale projects. You will work closely with our...

Fortrea is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.We are currently...

Job Title: Clinical Trial ManagerAbout the Role:This role is part of a dynamic, centralized study management team responsible for the execution of global clinical trials. As a Senior Clinical Trial Manager, you will be a key member of the study team, working independently and as part of a cross-functional partnership to plan, execute, and manage clinical...

As a leading global contract research organization with a passion for scientific rigor, MAI Fortrea Development Limited provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across multiple therapeutic areas.Fortrea is currently seeking a proactive Clinical Trial...

Key ResponsibilitiesThe successful Senior Clinical Data Specialist will be responsible for leading complex oncology clinical trials and ensuring timely delivery of high-quality data.They will develop and implement strategic plans for CDM deliverables, manage vendor contracts, and oversee budget management.The ideal candidate will have a strong understanding...

As a global leader in clinical development, Fortrea is seeking a proactive Clinical Trial Administrator to join our expanding team in Central London. This client-dedicated role is a great opportunity to work with a wide range of clinical trials and therapeutic areas.The ideal candidate will have at least 1-2 years of experience supporting clinical trials in...

Job Title OverviewThe Regulatory Affairs Project Manager will support the Regulatory Affairs Manager's vision and leadership by providing patient-centric and compliant regulatory expertise.  Key ResponsibilitiesSupport the business of the company, including involvement in product launches, acquisitions, and divestitures as a Regulatory Affairs...

Job Description:At MAI Fortrea Development Limited, we are seeking an experienced Clinical Research Associate to join our team. This is a full-time and permanent position.About the Role:We are currently recruiting for a CRA II in Scotland to work on a range of therapeutic areas, including Oncology, Haem-oncology & Immunology.Responsibilities:Conduct...

As a leading contract research organization (CRO) with a strong commitment to scientific excellence and decades of experience in clinical development, we provide pharmaceutical, biotechnology, and medical device customers a wide range of solutions across various therapeutic areas.We have over 19,000 staff conducting operations in more than 90 countries,...