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Hobson Prior is seeking a Clinical Trial Manager - Virology to join a biotechnology organization on a contract basis.

Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science. Hobson Prior is seeking a Clinical Trial Manager - Virology to join a biotechnology organization on a contract basis. In this role, you will oversee regional management of clinical trials (Phase Ib-III) with a focus on the EMEA region. You will work closely with global teams and external partners to ensure the successful execution of studies from start-up to close-out. This position requires a mix of onsite presence (3-5 days per week) and remote work. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: • Manage regional aspects of clinical trials, ensuring timelines and budgets are met., • Draft and review key study documents such as protocols, consent forms, and reports., • Collaborate with vendors and CROs to execute studies effectively., • Monitor study progress and address any issues that arise., • Train investigators, coordinators, and vendors on study requirements., • Oversee site budget and contract processes., • Support data review and preparation of study reports., • Contribute to study logistics, planning, and stakeholder management., • Provide expertise on country-specific regulations and site suitability., • Participate in cross-functional team activities and initiatives. Key Skills and Requirements: • Background in a scientific discipline or nursing qualification., • Experience in managing or coordinating clinical studies., • Familiarity with virology is beneficial but not essential., • Knowledge of FDA, EU regulations, ICH guidelines, and GCP standards., • Strong organizational, communication, and problem-solving skills., • Ability to prioritize tasks and adapt to changing environments., • Monitoring or co-monitoring experience is desirable., • Willingness to travel internationally as needed. For more information, please contact Athi Singata. If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - .

Clinical Trial Manager - Virology, london (uxbridge). Hobson Prior is seeking a Clinical Trial Manager - Virology to join a biotechnology organization on a contract basis. Manage regional aspects of clinical trials, ensuring timelines and budgets are met.

Social network you want to login/join with:.Clinical Trial Liaison – Oncology (Europe, Field-Based).An innovative global biotech company is seeking a Clinical Trial Liaison to drive site and patient engagement for oncology trials across Europe, with a focus on breast cancer and other high-priority

Liaise with country offices and central team (Clinical Supply Operations, Operation Leads, Protocol Managers, Medical Monitor, Safety, Quality Person) to ensure that Clinical trial application activities are in compliance with study timelines, BMS SOPs, worldwide regulatory guidelines and regulation

Sign in to set job alerts for “Senior Clinical Trial Manager” roles. Clinical Trial Vendor Manager - Novartis Dedicated (home-based anywhere in Europe). Senior Clinical Trial Vendor Manager - Remote - FSP.

As a Clinical Trial Manager (CTM), you will oversee the planning, execution, and close-out of clinical trials to ensure they are conducted to the highest standards of quality, compliance, and patient safety. Lead and manage the execution of assigned clinical trials from start-up through to completio

Hobson Prior is seeking a Clinical Trial Manager - Virology to join a biotechnology organization on a contract basis. In this role, you will oversee regional management of clinical trials (Phase Ib-III) with a focus on the EMEA region. Manage regional aspects of clinical trials, ensuring timelines a

Working closely with Clinical Development, Clinical Operations, and external clinical trial site staff, the clinical scientist will ensure scientific integrity and operational excellence in AIRNA’s clinical trials. The Clinical Scientist supports the design, execution, and analysis of clinical tri

The Submission Manager, Clinical Trials manages and coordinates the timely, compliant, and accurate delivery of the core submission documents and dossiers to Bristol Myers Squibb (BMS) HA/EC Applicants and CRO. Prepare and distribute the global Clinical Trial Application dossier and subsequent subst

Join Us as a Clinical Trial Manager. The role will oversee trials in the UK, Ireland and the Nordics. If you thrive in a fast-paced, collaborative environment and have a passion for clinical excellence - this role is for you!.

In this role, you will oversee regional management of clinical trials (Phase Ib-III) with a focus on the EMEA region. Manage regional aspects of clinical trials, ensuring timelines and budgets are met. Hobson Prior is seeking a Clinical Trial Manager - Virology to join a biotechnology organization o

Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targete

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 Us as a Clinical Trial Manager. Ensure inspection readiness of assigned trials within country. The role will oversee trials in the UK, Ireland and the Nordics.

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

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

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

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. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career

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

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. Demonstrates core understanding of medical term

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 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

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

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

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

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. Clerkenwell Health is an innovative and leading Research Organisation specialising in the delivery of scientifically grounded

VP Global Clinical Trial Management. Reporting to the Senior Vice President Clinical Operations, you will be a key member of the executive leadership team, leading the Clinical Operations and Project Management functions operationally and strategically. VP Global Clinical Trial Management.

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. We are growing our Team and hiring a UK-homebased Clinical Trial Manager to work as a Clinical Ri

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

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

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

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

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

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. Minimum of 5 years of experience in clinical trial management, with a

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. Minimum of 7 years in clinical research in a CRO or Pharmaceutical/Biotechnology I

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 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. Data Management services meet the standards required to maintain UKCRC

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 potentially in Asia. Sales Executive – Pharmacovigilance/Clinical Trial IT Soluti

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

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

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. We are growing our Team and hiring a UK-homebased Clinical Trial Manager to work as a Clinical Ri

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. Clerkenwell Health is an innovative and leading Research Organisation specialising in the delivery of scientifically grounded

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

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

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

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. Compile and maintain project-specifi

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

As a Clinical Trial Manager, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. Develop core trial documents, trial plans, and system setups, ensuring operational excellence. BA/BS degree with at least 3 years of clinical tria

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

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

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