Regulatory Affairs Coordinator

The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization.The position holder responsibility includes the entire CSL product portfolio and development pipeline.Responsibilities include: -Acts as a Regulatory Intelligence Triage Manager, responsible for driving initial...

Job Overview:As the initial cohort of the Leasing Operations team for the region, this new role involves overseeing and streamlining leasing activities within a specific geographic area. The ideal candidate will be a skilled operational practitioner with a solid understanding of the end to end leasing operational process You will have the ability to...

Audit of Tax - Manager and Senior Manager Opportunities Reading We are seeking talented individuals to join one of the Big 4's Corporate Tax Team in at Manager and Senior Manager levels, where you'll undertake a mix of audit of tax and advisory work. Working with senior and experienced personnel in both the tax and audit lines of business will provide you...

Planning DirectorSouthampton£££ DOEMy client is an established Planning Consultancy, offering a range of Town Planning, Architecture, Urban Design and Ecology services across Southampton and surrounding areas. They are seeking and experienced and dynamic Planning Director who will be overseeing all aspects of the Planning process, from initial concept...

Job OverviewDevelop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor's requirements.Essential Functions Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text...

IQVIA's cFSP team are seeking a Clinical Trial Manager to join us on our mission to drive healthcare forward. Great opportunity to shape local component of global study (UK remit / 2 studies across 8-10 sites / phase I-III). Sponsor dedicated to one of the world's largest pharmaceutical companies. Fully remote with minimal travel. RESPONSIBILITIES Partner...

Come create the technology that helps the world act togetherNokia is committed to innovation and technology leadership across mobile, fixed and cloud networks. Your career here will have a positive impact on people's lives and will help us build the capabilities needed for a more productive, sustainable, and inclusive world.We challenge ourselves to create...

Job Description Our client, a pharmaceutical development company has a requirement for a Regulatory Affairs Director to join their UK team. This role is perfect for a senior manager/ experienced regulatory professional who is looking to head up Strategy implantation with focus of the UK and EU market in medicinal products. As Regulatory Affairs Director,...

Our client, a pharmaceutical development company has a requirement for a Regulatory Affairs Director to join their UK team. This role is perfect for a senior manager/ experienced regulatory professional who is looking to head up Strategy implantation with focus of the UK and EU market in medicinal products. As Regulatory Affairs Director, you will:...

IQVIA have a fantastic opportunity for a Regulatory Affairs Lead to work for a growing pharmaceutical company. You will be joining a small team responsible for a range of products and therapy areas. It is a fantastic time to join the company as they are lots of growth potential and exciting plans for the near future. The role is a permanent, headcount...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in...

The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territories and to register several of development projects into the international region. This role is key to driving both the Regulatory strategy and execution.• Provide...

The GPS Global Regulatory Affairs Life Cycle Management Team based at my clients site in Reading has a 1-year position available to build Medicinal Product capability in and outside Europe. We are looking to hire a candidate strongly interested in Regulatory Affairs - with experience in medicinal products. You will grow and maintain major portfolio in...

Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA page is loaded Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA Apply locations Reading, Berkshire, United Kingdom Solna, Sweden Amsterdam, Netherlands Barcelona, Spain Sofia, Bulgaria time type Full time posted on Posted 7 Days Ago job requisition id...

Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA page is loaded Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA Apply locations Reading, Berkshire, United Kingdom Solna, Sweden Amsterdam, Netherlands Barcelona, Spain Sofia, Bulgaria time type Full time posted on Posted 7 Days Ago job requisition id...

The Placement Team plays a pivotal role in ensuring the compliance, quality assurance and administration of student placements within the curriculum which can be a core and mandatory aspect of our students professional training or an optional element of the programme. The Placement Operations Coordinator role will include a wide range of duties involving...

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

**About the project** We're looking for a Configuration Coordinator to support the delivery of a professional QC service to a Defence project within resource, programme and budgetary constraints, which satisfies legislative, regulatory and company requirements The Configuration Team are responsible for the maintenance of the Configuration Management...

The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization.  The position holder responsibility includes the entire CSL product portfolio and development pipeline.Responsibilities include: -Acts as a Regulatory Intelligence Triage Manager, responsible for driving...

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the development...

The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline. Responsibilities include: - Acts as a Regulatory Intelligence Triage Manager, responsible for driving...

Job DescriptionAssociate Marketing Director - Multiple SclerosisThe purpose of this position is to manage the marketing and product materials as an innovative CNS pharmaceutical company prepares to introduce its first Multiple Sclerosis product to the UK market. Activities will include strategic planning and launch campaign preparation. The ideal candidate...

Job Description Associate Marketing Director - Multiple Sclerosis The purpose of this position is to manage the marketing and product materials as an innovative CNS pharmaceutical company prepares to introduce its first Multiple Sclerosis product to the UK market. Activities will include strategic planning and launch campaign preparation. The ideal...

**Job description** As a constantly changing and increasingly high-profile field, Tax can offer a surprisingly broad range of career paths to ambitious apprentices. As part of a dynamic and successful area of our business, our Tax teams work with a wide range of organisations and individuals, helping them to implement the tax approaches that best suit their...