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Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan. Significant clinical trial management experience in the area of oncology. You love having responsibility and a say in how clinical trials are run.

The Clinical Risk Manager role demands a solid clinical trial management experience within an industry setting as you will need to demonstrate a proactive approach to managing risk in clinical research. Ideally, 7 years work experience in life sciences or medically related field, including 4 years o

You will be central to the delivery of clinical trials, ensuring compliance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Home Office regulations. Support training and supervision of junior staff, and deliver clinical trial training across teams. If you're passionate abou

The post holder will be responsible for designing, implementing, and maintaining database systems and resources for the recording of clinical trials data, ensuring that they are compliant with appropriate regulatory requirements. About you: You will have significant data management experience, withi

The Clinical Risk Manager role demands a solid clinical trial management experience within an industry setting as you will need to demonstrate a proactive approach to managing risk in clinical research. Clinical Trial Managers candidates who are ready to take a leading role in a new team of Clinical

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our. Communicate and collaborate on global study activities; working clo

Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders. Must have knowledge of protocol and clinical drug development processes, clinical tria

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Candidates should expect to have an

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Nephrology are welcome to continue to work in their area of expertise or t

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Our global Clinical Operations colleagues within our PPD clini

Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders. Must have knowledge of protocol and clinical drug development processes, clinical tria

As a Clinical Trial Manager, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. BA/BS degree with at least 3 years of clinical trial experience, or an advanced degree with at least 2 years. Develop core trial documents, trial

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career

How many years of oncological therapeutic experience do you have as a Clinical Research Associate ,Clinical Lead and/or Clinical Trial Manager? Please list the oncological trials you had been working on, including the indication and phase of the trial. How many years of experience as a Clinical Lead

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Communicate and collaborate on globa

Support the Global Clinical Trial Manager, Global Early Clinical Development Manager, Local Trial Manager, Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials. Work with the clinical trial management staff to support

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Candidates should expect to have an

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Our global Clinical Operations colleagues within our PPD clini

Drives and leads the successful execution, oversight and approval of all clinical trial documents and operational plans of global clinical trials using strong project management, leadership, and organizational skills. Represents Global Clinical Operations (GCO) within the Global Trial Team and serve

Sales Executive – Pharmacovigilance/Clinical Trial IT Solutions (Life Sciences). Reporting to our VP of Sales & Marketing in Paris, you will be responsible for selling our Pharmacovigilance and Clinical Trials solutions to clients in the life sciences and healthcare sectors located in Europe, and

Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) are vital in ensuring our clinical research programs are executed with quality and excellence, providing the care and passion patients deserve. At least 2 years’ experience as a Clinical Trial Manager, Clinical Operations Leade

Plan logistics and resource usage for clinical trials, including the allocation of staff, equipment, and materials, to ensure that trials are conducted smoothly and without delays. Sr Clinical Trial Manager (Sponsor Dedicated) UK. Ensure compliance with applicable regulations globally and by region,

The role of the Senior Clinical Trial Administrator (Sr CTA) is to perform daily administrative activities and support the Project Manager(s), Project Director(s) and cross-functional study team(s) through expert knowledge and effective use of the systems, tools and processes available with a focus

You will be central to the delivery of clinical trials, ensuring compliance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Home Office regulations. Support training and supervision of junior staff, and deliver clinical trial training across teams. If you're passionate abou

As a Clinical Trial Manager you will take overall responsibility for the day-to-day management of multi-centre randomised clinical trials. Previous experience of working in a UKCRC registered clinical trials unit and previous involvement in development of clinical reporting forms are desirable. You

In response to emerging industry needs, we expanded our services to include Scout Clinical, one of the top providers of clinical trial patient travel and reimbursements, and Scout Academy, our secure, online, on-demand learning management system that ensures global compliance. The Scout Clinical Tri

Provide day-to-day oversight of Clinical Research Associate (CRA) tasks on assigned projects; provide oversight of the CRA’s management of sites and monitoring of the clinical trial data; review and approve site trip reports and escalate site issues as needed to trial assigned Director, CTI execut

The Clinical Risk Manager role demands a solid clinical trial management experience within an industry setting as you will need to demonstrate a proactive approach to managing risk in clinical research. Ideally, 7 years work experience in life sciences or medically related field, including 4 years o

Join Worldwide Clinical Trials for an unparalleled CRO experience, where you can drive extraordinary scientific breakthroughs and contribute to the very heart of every successful clinical trial. Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role. We are Worldwide Clinic

This has been driven by the successful delivery of clinical trials of the highest standards, through their people, innovation and transparency. VP Global Clinical Trial Management. Reporting to the Senior Vice President Clinical Operations, you will be a key member of the executive leadership team,

The Clinical Risk Manager role demands a solid clinical trial management experience within an industry setting as you will need to demonstrate a proactive approach to managing risk in clinical research. Clinical Risk Manager / Clinical Trial Manager. Clinical Risk Manager / Clinical Trial Manager.

You will be central to the delivery of clinical trials, ensuring compliance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Home Office regulations. Support training and supervision of junior staff, and deliver clinical trial training across teams. If you're passionate abou

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred;. Project Manager/Clinical Tria

Drives and leads the successful execution, oversight and approval of all clinical trial documents and operational plans of global clinical trials using strong project management, leadership, and organizational skills. Leads the development of the clinical trial strategy and delivers the clinical ope

Clinical Research Experience required, including at least 1 year of experience in Clinical Trial Management. Collaborates with cross functional internal and external stakeholders to ensure timely execution, budget execution of clinical trial deliverables within the country. Primary point of contact

Drives and leads the successful execution, oversight and approval of all clinical trial documents and operational plans of global clinical trials using strong project management, leadership, and organizational skills. Leads the development of the clinical trial strategy and delivers the clinical ope

As a Clinical Trial Vendor Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working fully embedded within a growing, top 5 Pharmaceutical company, you will be independently managing all vendor related aspects o

The Opportunity:As the Clinical Trial Lead, you will be accountable for the planning, set-up and execution of assigned drug trials, which may include: pre/post-proof of concept (POC) interventional drug trials, Clinical Pharmacology normal healthy volunteer clinical trials, pre-approval access and p

Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders. Must have knowledge of protocol and clinical drug development processes, clinical tria

The role of the Senior Clinical Trial Administrator (Sr CTA) is to perform daily administrative activities and support the Project Manager(s), Project Director(s) and cross-functional study team(s) through expert knowledge and effective use of the systems, tools and processes available with a focus

Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in the performance of clinical trial management activities. Candidates should expect to have an intensive training period and show the desire a

As a Senior Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Contribute to quality Site Selection through participation in site feasibility ensuring consistent conduct of pre-trial assessment vis

Working as a Senior Clinical Vendor Manager at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. In this role, you will be independently accountable for all vendor related oper

A degree in a relevant biomedical subject and relevant work experience in clinical trial management or as a clinical research nurse. Trial Administrators are responsible for the administration and collection of clinical research data for one or more cancer trial protocols. Ensure smooth day-to-day r