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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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📑 *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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📑 Global Biotech company with US Headquarters outside Boston, MA is expanding. Looking for Dynamic Leader to work remotely (possible meetings and functions each quarter in Waltham, MA office) The AD, Monitoring Oversight is responsible for Oversight and implementing a global sponsor oversight monitoring program within the clinical operations depart ...

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📑 Global Biotech company with US Headquarters outside Boston, MA is expanding. Looking for Dynamic Leader to work remotely (possible meetings and functions each quarter in Waltham, MA office) The AD, Monitoring Oversight is responsible for Oversight and implementing a global sponsor oversight monitoring program within the clinical operati ...

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📑 InterQuest are currently supporting a well established Pensions, Wealth & Incentive services organization to identify a Global Head of Compliance to join the organisation on a permanent basis.The role would hold oversight of the global compliance framework across the globe ensuring a positive compliance culture in embedded. The role holder would ac ...

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📑 InterQuest are currently supporting a well established Pensions, Wealth & Incentive services organization to identify a Global Head of Compliance to join the organisation on a permanent basis.The role would hold oversight of the global compliance framework across the globe ensuring a positive compliance culture in embedded. The role holder would ac ...

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📑 Director of DevOps/Cloud Platform EngineeringWho are weSimplifyVMS is a leading global SAAS provider of contingent workforce VMS solutions and is one of the fastest growing extended workforce technology providers globally. Ranked by various industry analysts a leading platform SimplifyVMS continues to evolve and be the pioneer for the larger extend ...

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📑 Director of DevOps/Cloud Platform EngineeringWho are weSimplifyVMS is a leading global SAAS provider of contingent workforce VMS solutions and is one of the fastest growing extended workforce technology providers globally. Ranked by various industry analysts a leading platform SimplifyVMS continues to evolve and be the pioneer for the larger extend ...

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📑 Associate Director Quality AssuranceSUMMARY:The Associate Director, Quality Assurance is tasked with implementing strategies to ensure successful delivery of high-quality Clinical Trials studies. This involves driving effective and efficient global processes within the realm of Quality and Operations. This leader collaborates closely with the Clini ...

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📑 Associate Director Quality AssuranceSUMMARY:The Associate Director, Quality Assurance is tasked with implementing strategies to ensure successful delivery of high-quality Clinical Trials studies. This involves driving effective and efficient global processes within the realm of Quality and Operations. This leader collaborates closely with the Clini ...

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📑 About the jobGlobal Performance and Analytics ManagerLocation: United Kingdom (remote), Spain (Madrid) Reporting to: VP Global Performance, Analytics & Ops SupportSwissport was incorporated in 1996. From its beginnings with operations at Switzerland's largest airports in Zurich, Geneva and Basel, Swissport has developed into a global leader. Today, ...

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📑 About the jobGlobal Performance and Analytics ManagerLocation: United Kingdom (remote), Spain (Madrid) Reporting to: VP Global Performance, Analytics & Ops SupportSwissport was incorporated in 1996. From its beginnings with operations at Switzerland's largest airports in Zurich, Geneva and Basel, Swissport has developed into a global leader. Today, ...

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📑 ADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and Computer Systems Compliance (CSC) (toget ...

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📑 ADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and Computer Systems Compliance (CSC) (toget ...

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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 19,0 ...

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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 19,0 ...

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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 19,0 ...

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📑 Join an innovative team dedicated to transforming healthcare! We're seeking a dynamic leader to serve as Country Head UK for our Global Clinical Operations (GCO) team, located near High Wycombe, UK.As the Country Head UK GCO, you'll spearhead strategic and operational management of clinical research and development activities, ensuring seamless exe ...

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📑 Join an innovative team dedicated to transforming healthcare! We're seeking a dynamic leader to serve as Country Head UK for our Global Clinical Operations (GCO) team, located near High Wycombe, UK.As the Country Head UK GCO, you'll spearhead strategic and operational management of clinical research and development activities, ensuring seamless exe ...

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📑 We are recruiting for a leading global organization dedicated to promoting excellence across industries, including Built Environment, Food, Healthcare, and ICT. As an auditor, you'll leverage your expertise in information security to assist businesses in achieving cybersecurity resilience. You'll play a vital role in auditing clients against nation ...

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📑 We are recruiting for a leading global organization dedicated to promoting excellence across industries, including Built Environment, Food, Healthcare, and ICT. As an auditor, you'll leverage your expertise in information security to assist businesses in achieving cybersecurity resilience. You'll play a vital role in auditing clients against nation ...

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📑 Guidant Global are currently seeking a number of accomplished Team leaders to join our growing teams. We are looking for individuals with experience training, leading, developing, and supervising team performance. Within this role you will oversee and nurture direct reports who are responsible for a variety of case handling duties, ensuring excelle ...

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📑 Job PurposeAs a Global Clinical Project Manager you are responsible for the management of all aspects of the Clinical Study Team activities for assigned clinical studies. The Global CPM, in concert with the Director Clinical Operations, is accountable for achieving successful execution and delivery of Moonlake´s clinical development team activities ...

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📑 Our client a global organisation.This role will support their People Operations Globally post transformation, you will have responsibility for MENA, APAC and the Americas and support the delivery of HR Operations including the COE and Shared Service Function.Experience globally with Shared Services, change and transformation within a complex matrix ...

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📑 Our client a global organisation.This role will support their People Operations Globally post transformation, you will have responsibility for MENA, APAC and the Americas and support the delivery of HR Operations including the COE and Shared Service Function.Experience globally with Shared Services, change and transformation within a complex matrix ...

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📑 HEAD OF FRAUDUP TO £110,000REMOTE (travel to UK-based and international offices required, offices based in London, Dublin, Leeds, and Malta)This role does not offer sponsorship.This is an exciting new opportunity to lead the company's Fraud Strategy, Fraud Operations and Payments Operations teams across gambling brands. You will be driving forward ...

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📑 HEAD OF FRAUDUP TO £110,000REMOTE (travel to UK-based and international offices required, offices based in London, Dublin, Leeds, and Malta)This role does not offer sponsorship.This is an exciting new opportunity to lead the company's Fraud Strategy, Fraud Operations and Payments Operations teams across gambling brands. You will be driving forward ...

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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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📑 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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📑 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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📑 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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📑 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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📑 The Opportunity: We are looking for a strategic regulatory leader to join our growing regulatory team at Relay Tx. You will have the opportunity to ​help define and implement innovative regulatory strategies to expedite the development and approval of our transformative pipeline. You will serve as the regulatory representative on relevant proje ...

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📑 Clinical Project Manager The Study Lead Country Operations (SLCO) is the primary point of contact for the Country Operations (CO) team at the global study level and will act as a core study team member. The SLCO will be accountable for coordinating and driving activities performed by country operations including start up, monitoring, site overs ...

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📑 Remote within the country The country Clinical Research Lead (CRL) responsibilities include operational delivery of strategic clinical studies assigned to the country, to support client's pipeline, in accordance with ICH/GCP, client SOPs, local operating guidelines and local requirements, as applicable. CRL works locally, supporting Associate Di ...

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📑 Country Head UK, Global Clinical Operations Johnson & Johnson Innovative Medicine has an ambitious vision to integrate digital into the core of how we work amplifying our core capabilities and making a positive difference to the lives of patients, healthcare professionals, our employees and our communities.We have an exciting opportunity f ...

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📑 Country Head UK, Global Clinical Operations Johnson & Johnson Innovative Medicine has an ambitious vision to integrate digital into the core of how we work amplifying our core capabilities and making a positive difference to the lives of patients, healthcare professionals, our employees and our communities. We have an exciting opportunity ...

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📑 The Opportunity: We are looking for a strategic regulatory leader to join our growing regulatory team at Relay Tx. You will have the opportunity to ​help define and implement innovative regulatory strategies to expedite the development and approval of our transformative pipeline. You will serve as the regulatory representative ...

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📑 Description Director - Quality Assurance Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening dise ...

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📑 Job Purpose The Senior Study Leader is the leader of the cross-functional clinical trial team (CTT), guides planning and management of the assigned clinical study/studies end-to-end to achieve objectives. Accountable for proactive, iterative operational planning with effective contingencies and embedded risk management mindset in CTT. Oversee b ...

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📑 Toxicologist / Safety Assessor - 2407019155W **Description** Kenvue is currently recruiting for: **Toxicologist / Safety Assessor** This position reports into the Safety Assessor Manager and is based at High Wycombe, United Kingdom. **Who We Are** At Kenvue ( , we reali ...

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📑 Job PurposeAs a Global Clinical Project Manager you are responsible for the management of all aspects of the Clinical Study Team activities for assigned clinical studies. The Global CPM, in concert with the Director Clinical Operations, is accountable for achieving successful execution and delivery of Moonlake´s clinical develop ...

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📑 Senior Manager Global Quality Operations (Senior PV Auditor)This is a home-based role offering a fantastic package including generous salary, incentive bonus, home based allowance plus much more. My client a Global pharmaceutical company are seeking an experienced Senior Manager, Global Quality Operations to manage and perform audits with focus on ...

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📑 Senior Manager Global Quality Operations (Senior PV Auditor)This is a home-based role offering a fantastic package including generous salary, incentive bonus, home based allowance plus much more. My client a Global pharmaceutical company are seeking an experienced Senior Manager, Global Quality Operations to manage and perform audits with focus on ...

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📑 Remote within the country The country Clinical Research Lead (CRL) responsibilities include operational delivery of strategic clinical studies assigned to the country, to support client's pipeline, in accordance with ICH/GCP, client SOPs, local operating guidelines and local requirements, as applicable. CRL works locally, s ...

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📑 Norman Broadbent PLC, a leader in executive search, is delighted to be partnering with a global medical devices company on the appointment of a Head of Regulatory Affairs. Reporting to the Chief Technical Officer, the successful candidate will lead the interpretation of product and device regulation and the translation of that regulation to the bus ...

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📑 Norman Broadbent PLC, a leader in executive search, is delighted to be partnering with a global medical devices company on the appointment of a Head of Regulatory Affairs. Reporting to the Chief Technical Officer, the successful candidate will lead the interpretation of product and device regulation and the translation of that regulation to the bus ...

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📑 Career CategoryClinical DevelopmentJob DescriptionHOW MIGHT YOU DEFY IMAGINATION?If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnol ...

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📑 Provide oversight and leadership to Clinical Leads (CL) for project productivity, delivery and quality resulting in strong financial performance and customer satisfaction. Work with Clinical Lead (CL) teams to focus on leveraging deep therapeutic expertise and IQVIA solutions to drive operational excellence and strategic leadership with our custom ...

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📑 Managing Director - Europe P&L responsibility for £160M+ and 400+ employeesWe are seeking an experienced Managing Director to lead the European operations of a leading global manufacturer, recognised for its innovative solutions to industrial and resource sectors. This global organisation has a strong presence in Europe, operating in over 40 countr ...

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