Clinical Trial Manager

Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forwardWhy IQVIA?Growth potential - clear pathways to success for those who want to grow with usProfessional development - resources that promote your career growth and programs to help you build knowledge and gain skillsWork-life balance - leaders that support flexible...

Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forwardWhy IQVIA?Growth potential - clear pathways to success for those who want to grow with usProfessional development - resources that promote your career growth and programs to help you build knowledge and gain skillsWork-life balance - leaders that support flexible...

Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UKJoin us on our exciting journeyRemote/Hybrid/Office based working options.Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forwardAs Clinical Research Associate you will be responsible perform monitoring and site management work to ensure that...

Job Title: Regulatory Affairs Coordinator CTA, CTR (Consultant)Job Type: 12 Month Contract Location: Berkshire, UK – Hybrid Rate: £22-25 per hour PAYE (inside IR35)We are partnered with a leading Pharmaceutical organisation who are looking for a junior Regulatory Consultant to join on a 12-month contract basis. This role will be sat in the core regulatory...

Job OverviewThe Vice President Medical Strategy and Head of the Hematology/Oncology COE provides strategic medical and scientific leadership, subject matter experience and expertise to IQVIA and to IQVIA's clients in Hematology and Oncology. The overarching remit is to grow IQVIA's market share in hematology and oncology and will develop strategies toward...

Job OverviewThe Vice President Medical Strategy and Head of the Hematology/Oncology COE provides strategic medical and scientific leadership, subject matter experience and expertise to IQVIA and to IQVIA's clients in Hematology and Oncology. The overarching remit is to grow IQVIA's market share in hematology and oncology and will develop strategies toward...

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...

Our cFSP (sponsor dedicated) team are growing; join us on our mission to drive healthcare forwardWe are recruiting for a Senior Clinical Research Associate / Senior Clinical Research Associate II to assist our sponsor's hematology studies.Why IQVIA?Growth potential - clear pathways to success for those who want to grow with usProfessional development -...

Job Description SummaryJob Overview: Reviewing of the vendor and category related specific sections of the protocol, ensure vendor expertise is leveraged when refining specifications towards Final Protocol Contributing to development of Study Specification Worksheet (SSW) to facilitate bid process and selection of Vendors. Quote/Proposal review in...

Job Description SummaryJob Overview:• Reviewing of the vendor and category related specific sections of the protocol, ensure vendor expertise is leveraged when refining specifications towards Final Protocol• Contributing to development of Study Specification Worksheet (SSW) to facilitate bid process and selection of Vendors.• Quote/Proposal review in...

Are you ready to make a meaningful impact on patients' lives while driving sales growth in the healthcare sector? Due to continued growth, Coloplast is seeking a motivated and dynamic individual to join us in the role of Bowel Management Territory Manager.Location - Oxfordshire / Berkshire / SouthamptonMore about the roleAs a vital member of our team, you'll...

Reading, RG1 6ABClosing date: 23rd May 2024The Salvation Army are partnering with the University of Stirling via the Salvation Army Centre for Addiction Services and Research to deliver a trial for the National Institute for Health and Care Research (NIHR). This unique and innovative social care trial will examine the effectiveness and cost effectiveness of...

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...

We are growingIf you are interested in applying for this job, please make sure you meet the following requirements as listed below.Senior MSK Physiotherapist wanted Minimum 3 years experience in MSK required preferably 5. Job description below please get in touch via linked in or email your to - #hiring #physiotherapyJob description - Senior MSK...

About AbbottAbbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.The Opportunity Abbott Rapid Diagnostics is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry...

A well-managed and friendly MSK Clinic in Reading is looking for an experienced Musculoskeletal Physiotherapist to join their friendly service for an ongoing locum contract. The hourly pay rate for this role is £27 - £31 P/H all-inclusive.Requirements:You will be expected to meet the below key requirements: Have a minimum of 12-18 months of MSK experience,...

Psychology Tools () is an online platform publishing evidence-based therapy resources for clinical professionals. We are growing fast and looking to fill a number of roles in our Business Development & Customer Success team. You will join a small team based in our Reading office near to Reading Station. Due to data security requirements, postholders will be...

Looking for a new challenge and more flexible working hours that fit in with your work life balance? Then look no further Our Community Nursing team in Wokingham, Berkshire is recruiting for District Nurses / Community Nursing Sisters / Charge Nurses.In this role, you will provide support and leadership to a great team and join a team that provides a...

Business ContextPrimark is a leading global fashion retailer, with over 450 stores across 16 countries and employing over 72,000 people.This is an exciting time for Primark, with ambitious growth plans and a transformation agenda to match: Expansion into new markets and continued growth within existing markets Delivering more memorable in-store experiences...

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...

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 ...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to administratively and...

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...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific documentation...

Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives. Essential Functions • Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work,...

As a Director within the Strategic Site Solutions team, you will be responsible for developing and delivering site-based network strategies to deliver growth, differentiation, and superior performance across the IQVIA human data science business. The role is focused on growing and maintaining two regional site networks, a Cell & Gene Therapy site network and...

As a Director within the Strategic Site Solutions team, you will be responsible for developing and delivering site-based network strategies to deliver growth, differentiation, and superior performance across the IQVIA human data science business. The role is focused on growing and maintaining two regional site networks, a Cell & Gene Therapy site network and...

As a Clinical Project Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The CPA will interact on a global scale within the study team and clinical team. The CPA sphere of influence and communication will include the Global Clinical Lead, the Clinical Project Manager,...

Vendor Program Manager Key accountabilities  Provides vendor oversight and management at a trial level to ensure all vendors deliverables are done timely & good quality Coordinates vendor deliverables across VSE during study start-up Covers all vendor activities after study start-up and all categories not covered by VSEs: Drives and monitors...

Job Purpose Responsible for efficient and appropriate management of Trial Master Files (TMF) and other TMF related, inspection relevant documents from creation through archival in compliance with applicable SOPs, processes and study specific requirements for assigned trials according to established timelines. Main Duties Drive TMF Quality at trial...

Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward! Why IQVIA? Growth potential - clear pathways to success for those who want to grow with us Professional development - resources that promote your career growth and programs to help you build knowledge and gain skills Work-life balance - leaders that...

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare...

About us: **About the role**: As the Ostomy Clinical Resource Specialist based in Ohio, you will play a pivotal role in driving profitable business results through the execution of Convatec's current business strategies. Your key responsibility will be to foster high-level customer relationships by providing essential clinical support to our dynamic sales...

**Clinical Sales Specialist - Wound Closure - UK** As part of a team expansion project across the EU, IQVIA is recruiting for several field-based sales positions in France, Netherlands, Italy, Germany, and the UK on behalf of our client - a highly respected global company renowned for its innovation and success within pharmaceutical, consumer health and...

Introduction If you are an experienced Senior Nurse looking for the next step in your career, or an existing Clinical Services Manager looking for a new opportunity, then join our friendly team at Rosebank House in Reading. Working 37.5 hours per week, you will join the multidisciplinary team providing person-centred care and rehabilitation for male...

It is a very exciting time at ICON - we’re a world-leading healthcare intelligence and clinical research organisation. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the...

Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UKJoin us on our exciting journey!Remote/Hybrid/Office based working options.Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!As Clinical Research Associate you will be responsible perform monitoring and site management work to ensure that...

Role Overview: The Site Enablement Solutions team at IQVIA provides qualified, clinically experienced research staff to clinical trial sites globally to accelerate and optimize the performance of clinical trials. By supplying sites with support for data entry, patient recruitment, patient visits, assessments, and other tasks, IQVIA is able to relieve the...