📑 Gabriel Roberts is working with a startup CRO who are looking for their first CTA to join their small but passionate team! My client has very strong core values which results to a great work environment and very happy staff! This role is working in remotely in the UK. This is a unique opportunity to grow with a company an ...
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📑 We are currently seeking a talented and experienced Senior Regulatory Affairs Manager to join our client's team in Surrey. Our client is an established cosmetics/pharmaceuticals company looking for someone with expertise in global cosmetic regulations. In collaboration with a highly skilled international team you will help to manage the ...
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📑 Associate Director, Clinical Project Scientist (Oncology) - 2406181923W **Description** At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions ar ...
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📑 Jordan Griffiths is currently seeking a highly motivated Clinical Research Associate (CRA) to join our top CRO client. As a CRA, you will be responsible for the execution and management of clinical trials across various therapeutic areas in South West England.Key Responsibilities: Conduct site initiation, monitoring, and close ...
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📑 Precision for Medicine is seeking an experienced Senior Clinical Data Associate to provide comprehensive data management support throughout all phases of the clinical trial data management process. Under direct supervision, you will ensure adherence to Standard Operating Procedures (SOPs), regulatory guidelines, and study-specific plans. This ro ...
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📑 The Associate Engineer, R&D Software Engineering is responsible for the specification and design of software to meet defined requirements by following agreed design standards and principles. Clario is a 50+ year old company that delivers industry leading clinical trial endpoint technology solutions. The future of clinical trials is vibrant, with ...
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📑 Jordan Griffiths is currently seeking a highly motivated Clinical Research Associate (CRA) to join their top CRO clients. As a CRA, you will be responsible for the execution and management of clinical trials, ensuring adherence to study protocols, regulatory requirements, and timelines.Key Responsibilities: Conduct site initia ...
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📑 Smart Solutions are working with an award winning manufacturer based in Swansea. We are seeking for an enthusiastic experienced Clinical Trials Manager to join our Clinical and Application Research department. You will be responsible for all aspects of clinical trial management. The post holder will have a significant level of responsibility. Dutie ...
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📑 At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science ...
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📑 About this job : As the Manager of Clinical Transparency, your role is pivotal in overseeing and executing the clinical trial disclosure process for assigned studies conducted by Astellas globally. You will play a key part in ensuring compliance with clinical trial disclosure laws, industry guidance, and corporate policy. Your responsibili ...
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📑 Summary The Trial Coordinator will be a member of one or more trial working groups, responsible for the management and organisation of the trial(s) office for the conduct of large, clinical trial protocols and administration of the clinical collaborative groups. They are expected to be capable of the continued development, critical app ...
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📑 Every year 3 million documents are uploaded in the electronic Trial Master Files to preserve the story of the study and ensure innovative medicines can reach even more patients worldwide. But in this world of digital and technological transformation, we must also continue to evolve our approaches to clinical document management and unleash the powe ...
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📑 Role: Clinical Trial Assistant (CTA / Associate CPM) Location: Hybrid (4 days remote and 1 day per week in London)Company: Small Biopharmaceutical Company Salary: £35,000 - £42,000 (depending one experience) RBW Consulting are excited to announce an exciting opportunity to join a unique small pharmaceutical client of ours. They are pioneering techn ...
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📑 Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medi ...
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📑 Gabriel Roberts is working with a startup CRO who are looking for their first ever Clinical Trial Managers to join their small but passionate team! My client has very strong core values which results to a great work environment and very happy staff! This role is working in remotely in the UK. This is a uniqu ...
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📑 We have current opportunity for an experienced Clinical Trial Manager in Europe! Join our growing team.Precision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced ...
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📑 Role Overview The Senior Clinical Trial Manager works within the clinical trial team to provide regional trial oversight and ensures deliverables are met in terms of quality, compliance, and timing. Strong vendor management is critical for this role. The position will report to the Director, Clinical Operations. This role may work collaboratively o ...
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📑 Role Overview The Senior Clinical Trial Manager works within the clinical trial team to provide regional trial oversight and ensures deliverables are met in terms of quality, compliance, and timing. Strong vendor management is critical for this role. The position will report to the Director, Clinical Operations. This role may work collaboratively o ...
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📑 Job Title: Patient Engagement Sr Mgr Global Trial Optimization Department: 1467-Global Clinical Trial ServicesSUMMARY:The Senior Manager, Global Trial Optimization (GTO), Patient Engagement will lead program or study level Patient Recruitment and Retention Strategy development to inform the clinical strategy, study protocols and operational plans t ...
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📑 We’re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid.The Role:Deliver CTA regulatory strategies and operations for a designated port ...
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📑 Precision for Medicine is hiring a Senior/Principal Quality Auditor to join our team, candidates can be based in either UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.Position Summary:The Senior/Principal Quality Auditor supports the audit program and clinical projects to ensure compliance with regulations and Precisi ...
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📑 We are currently looking for a Qualified Person (QP) to join a pharmaceutical company based in Northern Ireland. Salary & Benefits £77,000 per annum Comprehensive benefits package offered The Role Operate within the Code of Practice for Qualified Persons in the pharmaceutical in ...
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📑 100,000+ That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medici ...
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📑 Cure Talent are delighted to be partnered with an established Medical Devices Manufacturer, who, due to their continued growth, have an exciting opportunity for an experienced Clinical Research to join them. As the new Clinical Research Associate, you will be responsible for overseeing trial sites, managing trial data, ensuring compliance with regu ...
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📑 Walker Cole International is searching for a Clinical Program Manager to join an industry leading pharmaceutical business specialising in Cell and Gene Therapy. As a Clinical Program Manager you will be responsible for oversight of all UK Clinical trial activity.Your responsibilities as the Clinical Program Manager will be:Liaise with key academic, ...
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📑 Walker Cole International is searching for a Clinical Program Manager to join an industry leading pharmaceutical business specialising in Cell and Gene Therapy. As a Clinical Program Manager you will be responsible for oversight of all UK Clinical trial activity.Your responsibilities as the Clinical Program Manager will be:Liaise with key academic, ...
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📑 Life Sciences Recruitment is pleased to confirm that we are working with a rapidly growing, global client that provides a variety of unique clinical trial services to the Life Science industry with a key focus on secondary packaging and labelling.We're looking for a full-time Business Development Manager with extensive experience in working in end- ...
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📑 100,000+ That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medici ...
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📑 *Background must be in pharma NOT medical devices)Senior R&D QA GCP Auditor (pharmaceuticals)I'm looking to recruit a seasoned Senior R&D QA GCP Auditor responsible for ensuring compliance and proper implementation of Good Clinical Practice (GCP) and Good Clinical Laboratory Practice (GCLP) within the clinical development of Global R&D projects in ...
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📑 100,000+ That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations is Novartis’ new powerhouse, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medicine ...
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📑 Company Overview: Join our client a specialist pharmaceutical supply business dedicated to advancing healthcare through innovative services. Who are seeking a Remote Key Account Manager based in the UK to support their growing client base. Position Overview: As a Key Account Manager, you'll manage key client relationships in the biopharmaceutical a ...
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📑 The Role The Associate Director will manage multiple studies and projects and will be a core member of the clinical operations team. Lead the clinical trial strategy, operations, and large-sized global project teams with innovative and strategic perspective. Demonstrate strong stakeholder relationship, a positive working culture and act as ...
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📑 Cure Talent are delighted to be partnered with an established Medical Devices Manufacturer, who, due to their continued growth, have an exciting opportunity for an experienced Clinical Research to join them.As the new Clinical Research Associate, you will be responsible for overseeing trial sites, managing trial data, ensuring compliance wi ...
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📑 Cure Talent are delighted to be partnered with an established Medical Devices Manufacturer, who, due to their continued growth, have an exciting opportunity for an experienced Clinical Research to join them.As the new Clinical Research Associate, you will be responsible for overseeing trial sites, managing trial data, ensuring compliance wi ...
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📑 Regulatory Affairs AssociateThe Regulatory Affairs Associate will be responsible for:• Managing the clinical trial applications in Europe and other selected countries • Keeping up to date with regulatory and legal changes in EU• Preparing pre- and post-authorisation regulatory documentation and applications • Assisting in marketing access activitie ...
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📑 As a pharmaceutical support industry leader, UBC is devoted to empowering health solutions for a better tomorrow . We take pride in improving patient outcomes and advancing healthcare . At UBC, we provide services to enhance the entire drug development process and commercialization lifecycle - from clinica ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. What you will be doing: Responsible for planning, mana ...
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📑 The Role The Associate Director will manage multiple studies and projects and will be a core member of the clinical operations team. Lead the clinical trial strategy, operations, and large-sized global project teams with innovative and strategic perspective. Demonstrate strong stakeholder relationsh ...
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📑 An exciting opportunity to join a innovative organization committed to the advancement of cell and gene therapies as Director of ATTC Network Coordination.Ensures the creation of Advanced Therapy Treatment Centres within the NHS framework. The objective is to expand and fully integrate the network into the NHS and establish new sites for clinical t ...
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📑 An exciting opportunity to join a innovative organization committed to the advancement of cell and gene therapies as Director of ATTC Network Coordination.Ensures the creation of Advanced Therapy Treatment Centres within the NHS framework. The objective is to expand and fully integrate the network into the NHS and establish new sites for clinical t ...
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📑 The Role Responsible for the patients taking part in the study Ensuring study compliance in relation to the ICH-GCP Maintain patient records inclusive of patient’s response to the trial and effectively reporting adverse events as per protocol, providing medical treatment to all patients as required ...
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📑 An exciting opportunity to join an innovative organisationmitted to the advancement of cell and gene therapies as Director of ATTC Network Coordination.Ensures the creation of ATT Treatment Centres within the NHS framework in the UK.The objective is to expand and fully integrate the network into the NHS and establish new sites for clinical trials o ...
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📑 ICON: Global Clinical Trial Manager ICON United Kingdom Remote*1.5 – 2 years running global clinical trials with a CRO, Pharmaceutical or Biotechnology company*Pay is up to 64,000 British Pounds per yea*Must be located in the United Kingdo*Fully remoteResponsibilities: • Planning and management of clinical studies conducted by global development te ...
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📑 ICON: Global Clinical Trial Manager ICON United Kingdom Remote*1.5 – 2 years running global clinical trials with a CRO, Pharmaceutical or Biotechnology company*Pay is up to 64,000 British Pounds per yea*Must be located in the United Kingdo*Fully remoteResponsibilities: • Planning and management of clinical studies conducted by global development te ...
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📑 Clinical Trial Pharmacist - Permanent, onsite, London.Brief Description:The Trial Pharmacist will manage and over see the pharmacy duties for multiple clinical trials for this biotechnology company. Your responsibilities will be inclusive of supporting other staff members, medicinal product management and handling of samples.Desired Skills and Qual ...
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📑 Clinical Trial Pharmacist - Permanent, onsite, London.Brief Description:The Trial Pharmacist will manage and over see the pharmacy duties for multiple clinical trials for this biotechnology company. Your responsibilities will be inclusive of supporting other staff members, medicinal product management and handling of samples.Desired Skills and Qual ...
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📑 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 1 ...
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📑 Are you an experienced full service Project Manager in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology, Rare Disease or CNS? Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial ...
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📑 100,000+ That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medici ...
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📑 Role location - homebasedThe Senior Study Leader is responsible for the execution and delivery of the Global Clinical Operations (GCO), clinical studies in accordance with the Operational Execution Plan (OEP) and clinical study protocol. You will lead the cross-functional Clinical Trial Team (CTT) and guide the planning and mana ...
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