IQVIA Sponsorship Jobs

Job Overview (CRAs are encouraged to apply) This role is assigned to designated Delivery Unit(s), sponsor(s), business line(s), and/or specific tasks as defined by the Line Manager (LM). The purpose of this role is to implement and adapt the Global Quality Management Plan in alignment with the specific needs of the assigned scope. The CCQM supports business line staff in improving compliance with

Hospital Account Manager - Respiratory Location: North West England and North Wales Department: Commercial - Secondary Care Role Overview: We are seeking a highly motivated and strategic Hospital Account Manager to join our Respiratory team in the North West. This role is pivotal in driving advocacy and prescribing of respiratory medicines across secondary care. Key Responsibilities: Account Mana

Job Overview (CRAs are encouraged to apply) This role is assigned to designated Delivery Unit(s), sponsor(s), business line(s), and/or specific tasks as defined by the Line Manager (LM). The purpose of this role is to implement and adapt the Global Quality Management Plan in alignment with the specific needs of the assigned scope. The CCQM supports business line staff in improving compliance with

Essential Functions Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. Develop contract language, payment language and budget templates as required as applicable to the position Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studi

Overview We are seeking an experienced Senior Medical Writer to lead the development of high-quality clinical and regulatory documents supporting global regulatory submissions. This role plays a critical part in ensuring that documents such as Investigator's Brochures (IBs), Clinical Study Reports (CSRs), and marketing authorization applications (MAAs/NDAs/BLAs) are scientifically accurate, consis

Hospital Account Manager - Respiratory Location: North West England and North Wales Department: Commercial - Secondary Care Role Overview: We are seeking a highly motivated and strategic Hospital Account Manager to join our Respiratory team in the North West. This role is pivotal in driving advocacy and prescribing of respiratory medicines across secondary care. Key Responsibilities: Account Mana

Join Our Team as a Therapeutic Strategy Lead Are you passionate about creating innovative delivery strategies that meet customer needs? Do you thrive in a collaborative environment where you can make a real impact? If so, we have the perfect opportunity for you! Purpose As a Therapeutic Strategy Lead, you'll develop and implement effective delivery strategies tailored to customer needs during the

Job Overview: Responsible for ensuring delivery of high quality and timely TMF Quality Review activities for a portfolio of studies. Essential functions: Responsible for timely assessment of quality and completeness of TMFs for an assigned portfolio of studies. Ensure TMF Quality Review activities are conducted as per process, in adherence with quality standards and defined timelines. Identify and

Job Overview Assist in organizing and managing research projects including contribution to development of study protocols, reports and data collection methods, arranging and attendance at project meetings and traveling to client sites as needed. May assist in preparation of abstracts, manuscripts and oral presentations along with other related study documents. Essential Functions • Organizes and h

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s Site Management (multi-sponsor) team is growing and seeking experienced Clinical Research Associates. We are recognised as a 2026 "Glassdoor Best Place to Work in the UK" and 1 in our category on the 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!). Apply today and forge a caree

IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK Apply today and forge a career with greater purpose, make an impact and never stop learning! Responsibilities Perform site monitoring visits (selection, initiati

Job Overview Assist in organizing and managing research projects including contribution to development of study protocols, reports and data collection methods, arranging and attendance at project meetings and traveling to client sites as needed. May assist in preparation of abstracts, manuscripts and oral presentations along with other related study documents. Essential Functions - Organizes and h

Bring clinical research directly to patients - and make a real-world impact At IQVIA, we are driven by a single purpose: to help improve patients' lives by accelerating the development and delivery of innovative healthcare solutions. Our Remote Research Clinicians (RRC) model is transforming how clinical trials are delivered - bringing high-quality clinical services directly to patients, wherever

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s Site Management (multi-sponsor) team are seeking experienced Clinical Research Associates. We are recognised as a 2026 "Glassdoor Best Place to Work in the UK" and 1 in our category on the 2026 Fortune World’s Most Admired Companies list (for the FIFTH consecutive year!). Apply today and forge a career with greate

Clinical Pharmacist Type : Full-time, hybrid We are looking for pharmacists to join the team! Join us in this exciting role where you will utilise your clinical expertise and commercial acumen to support patients with chronic conditions in primary care settings. As a clinical pharmacist at Interface Clinical Services, an IQVIA business, your responsibilities will include aiding practices with clin

Associate Principal, Implementation Science & Mixed Methods Research IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. Patient Centered Solutions

Senior Data Scientist Data Science, Analytics, and Technology Solutions (DATS) Brighton, UK IQVIA is hiring to expand our dedicated Real-World Evidence (RWE) FSP team, working fully embedded within the environment of a leading pharmaceutical client. This Data Scientist role sits within our Data Science, Analytics, and Technology Solutions (DATS) team and will play a key role in designing, implemen

Department: Solution and Project Leadership, Real World Evidence (RWE) Solutions Role Overview IQVIA is seeking an experienced Associate Director Project Manager to lead the delivery of complex, high-visibility Real World Evidence (RWE) engagements. This role is accountable for end-to-end delivery excellence across one or more large or strategically important studies, ensuring projects are deliver

Location: Remote, candidates must be based in what of the selected locations. Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you’ll work closely with one sponsor, gaining deep knowl

Our client is recruiting a Key Account Manager to shape and direct the use of a specialist product for multiple sclerosis management across the South West of England/ South Wales You need: A proven track record working in secondary care ABPI qualification Good selling skills, commercial acumen and negotiating skills The ability to develop positive relationships with all key customers including

Location: Remote, candidates must be based in what of the selected locations. Join IQVIA's Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you'll work closely with one sponsor, gaining deep knowl

Our client is recruiting a Key Account Manager to shape and direct the use of a specialist product for multiple sclerosis management across the South West of England/ South Wales You need: A proven track record working in secondary care ABPI qualification Good selling skills, commercial acumen and negotiating skills The ability to develop positive relationships with all key customers including

Regulatory & Start-Up Specialist, IQVIA Biotech, UK Homebased IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Job Overview We are seeking a highly motivated Regulatory & Start-Up Specialist to support c

Job Overview Study Lead are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The Senior Clinical Lead is a member of the core project team responsible for clinical delivery of full service, large, multi-regional studies to meet contractual requirements and in accordance with (Standard Op

Job Overview: Responsible for ensuring delivery of high quality and timely TMF Quality Review activities for a portfolio of studies. Essential functions: Responsible for timely assessment of quality and completeness of TMFs for an assigned portfolio of studies. Ensure TMF Quality Review activities are conducted as per process, in adherence with quality standards and defined timelines. Identify

Regulatory & Start-Up Specialist, IQVIA Biotech, UK Homebased IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Job Overview We are seeking a highly motivated Regulatory & Start-Up Specialist to support c

Post-Trial Access Manager, Continued Access is accountable for the execution of multiple global PTA programs, of mild and moderate complexity, with minimal supervision. PTA here refers to the provision of investigational product for the intent of treatment, in a non-trial setting and under the care of a physician, following participation in a trial. PTA by this definition is governed by local laws

About the Role We are looking for a Clinical Product Specialist to join our client a medical equipment manufacturer with a presence in over 90 countries. This is an exciting opportunity for a clinically trained professional (ideally nursing background) who is passionate about education, collaboration, and making a real impact in healthcare. The roe will focus on nutrition and enteral feeding (dige

AI Science Consultant - AI-accelerated Clinical Development Join a Ground-Breaking AI Initiative at IQVIA IQVIA is assembling a world-class team to create large-scale AI solutions, leveraging cutting-edge machine learning architectures. Our mission is to integrate data across clinical, real-world, and biomedical sources, unlocking new insights into patient trajectories and transforming how we unde

IQVIA is searching for an experienced Clinical Product Specialist on behalf of our client, a medical equipment manufacturer with a presence in over 90 countries. In this field-based role, you will deliver high-quality clinical training, support product evaluations, and collaborate closely with the commercial teams to drive real impact in patient care. The company holds leading market positions in

Clinical Research Coordinator – Blackburn Are you looking for an opportunity in Clinical Research? Do you want to work for an industry-leading company? If so, come and join us. IQVIA is currently looking for a Clinical Research Coordinator/Site Research Assistant to support a clinical study. This is a short-term study assignment (6 months) , working 13 hours per week , supporting a site in Blackbu

Clinical Research Coordinator - London (Short-Term Assignment) Are you looking for an opportunity in Clinical Research? Do you want to work for an industry-leading company? If so, come and join us. IQVIA is currently looking for a Clinical Research Coordinator to support a short-term clinical study. This is a short-term study assignment (3 months) , working 24 hours per week , supporting a site in

Job Overview Supervise and manage an assigned team of CPMs and their subsidiaries, who manage or support project management activities to mitigate risk, control cost, project schedule and ensure quality, time and budget deliverables are completed to the Sponsor's satisfaction in accordance with applicable SOPs, policies and practices. Ensure that employees are trained, and individual development i

Clinical Research Coordinator – London (Short-Term Assignment) Are you looking for an opportunity in Clinical Research? Do you want to work for an industry-leading company? If so, come and join us. IQVIA is currently looking for a Clinical Research Coordinator to support a short-term clinical study. This is a short-term study assignment (3 months) , working 24 hours per week , supporting a site in

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s Site Management (multi-sponsor) team are seeking experienced Clinical Research Associates. We are recognised as a 2026 "Glassdoor Best Place to Work in the UK" and 1 in our category on the 2026 Fortune World’s Most Admired Companies list (for the FIFTH consecutive year!). Apply today and forge a career with greate

IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK Apply today and forge a career with greater purpose, make an impact and never stop learning! Responsibilities Perform site monitoring visits (selection, initiati

Nurse Advisor position to cover Southampton hospital delivering infusions within the hospital environment. Providing support to health care professionals and patients in the delivery of treatment of a specific medication in the form of an intravenous infusion given to patients in the hospital clinic setting. As a Nurse Advisor, you require: To be clinically competent in cannulation and delivery o

Job Overview Manage and support team of Data Management professionals to efficiently produce databases that meet customer requirements. Essential Functions - Provide expert review and guidance for production of Data Management deliverables including CRF/e-CRF, database design and set-up, validation definition and programming, Data Management Plan and database deliverables to internal and external

Join IQVIA on our mission to accelerate innovation for a healthier world IQVIA UK's Site Management (multi-sponsor) team are seeking experienced Clinical Research Associates. We are recognised as a 2026 "Glassdoor Best Place to Work in the UK" and 1 in our category on the 2026 Fortune® World's Most Admired Companies list (for the FIFTH consecutive year!). Apply today and forge a career with greate

Join our client's Foundation and help us protect grandparents worldwide through the award-winning FAST Heroes program. Active in more than 20 countries, FAST Heroes teaches children to recognise stroke symptoms and share that lifesaving knowledge at home. We're looking for an energetic Events & Individual Giving Manager to lead our UK and international fundraising events while building a national

System Design Project Manager - Interactive Response Technology (IRT) The main purpose of this role is to write the requirements of the assigned IRT studies and manage the implementation in a way that ensures all patients get treated with the right study drug as per the Sponsor's study protocol. This is a highly consultative position in which the PM needs to utilize their Cenduit IRT knowledge to

Join IQVIA on our mission to accelerate innovation for a healthier world IQVIA UK's Site Management team is growing and seeking experienced Clinical Research Associates. Apply today and forge a career with greater purpose, make an impact, and never stop learning! Responsibilities Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted

As a Principal Biostatistician , you will provide end‑to‑end statistical leadership and integration support across Phase II and Phase III studies , working closely with cross‑functional stakeholders in a fast‑paced, global environment. Key Responsibilities • Provide Principal‑level Biostatistics support for Phase II–III clinical trials • Independently lead SAP authoring and review • Support integr

Job overview As a Vendor Lead you will be a Single Point of Contact (SPOC) for supplier services at a trial level and be the first point for issue escalation during study start up, acting as a conduit for clear communication and robust daily oversight Main responsibilities Reviewing of the vendor and category related specific sections of the protocol, ensure vendor expertise is leveraged when refi

Job overview As a Vendor Lead you will be a Single Point of Contact (SPOC) for supplier services at a trial level and be the first point for issue escalation during study start up, acting as a conduit for clear communication and robust daily oversight Main responsibilities Reviewing of the vendor and category related specific sections of the protocol, ensure vendor expertise is leveraged when ref

Senior Global Trial Manager - Single Sponsor Are you experienced in managing late phase clinical trials at a global level? We are looking for a Senior Global Trial Manager to join our Single Sponsor Department . Join our global team and take ownership of delivering late-phase clinical trials that meet timelines, budgets, and quality standards. As a core Clinical Trial Team (CTT) member, you'll lea

Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Managem

Job Overview The Trial Informatics Senior Analyst supports the administration of the Veeva Clinical system and tools utilized by Development Operations. The Informatics Senior Analyst ensures standardization in the process for collection of metrics and data. Essential Functions Support the administration of reporting systems and prepare metric reports. Work with clinical study teams to ensure the

Job Overview The Trial Informatics Senior Analyst supports the administration of the Veeva Clinical system and tools utilized by Development Operations. The Informatics Senior Analyst ensures standardization in the process for collection of metrics and data. Essential Functions Support the administration of reporting systems and prepare metric reports. Work with clinical study teams to ensure th

Location: Remote, candidates must be based Spain, Portugal or UK. Join IQVIA's Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you'll work closely with one sponsor, gaining deep knowledge of thei

Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Managem

Clinical Pharmacist Type : Full-time, hybrid We are looking for pharmacists to join the team! Join us in this exciting role where you will utilise your clinical expertise and commercial acumen to support patients with chronic conditions in primary care settings. As a clinical pharmacist at Interface Clinical Services, an IQVIA business, your responsibilities will include aiding practices with clin

Job Purpose The Strategic Project & Transformation Project Manager – NCIM is accountable for the end-to-end planning, governance, and operational delivery of a global site payment tool (NCIM). The role ensures effective orchestration of GCO cross-functional inputs across Clinical, Finance, and IT, enabling standardized, compliant, and transparent clinical site invoice management globally. Role Des

Job Overview Acts as Lead Medical Writer on any type of writing project, including projects with multiple deliverables/components. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs senior review of all types of medical writing deliverables. Provides feedback and guidance to more junior st

We are seeking experienced Clinical Research Associates (CRA II and Senior CRA 1) across the UK to strengthen our cFSP sponsor-dedicated team. Why IQVIA? Career development and progression Supportive leadership and flexible ways of working A culture built on collaboration, trust, and innovation Awards IQVIA is a 2026 "Glassdoor Best Place to Work in the UK". IQVIA is recognised as 1 in its categor

Job Purpose The Strategic Project & Transformation Project Manager - NCIM is accountable for the end-to-end planning, governance, and operational delivery of a global site payment tool (NCIM). The role ensures effective orchestration of GCO cross-functional inputs across Clinical, Finance, and IT, enabling standardized, compliant, and transparent clinical site invoice management globally. Role Des

Job Overview Manage and support the operational elements and execution of studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction and in accordance with SOPs; policies and practices from pre-award to close-out. Work with study(ies)/program(s) teams to focus on leveraging deep therapeutic expertise and IQVIA solutions to drive

We are seeking experienced Clinical Research Associates (CRA II and Senior CRA 1) across the UK to strengthen our cFSP sponsor-dedicated team. Why IQVIA? Career development and progression Supportive leadership and flexible ways of working A culture built on collaboration, trust, and innovation Awards IQVIA is a 2026 "Glassdoor Best Place to Work in the UK". IQVIA is recognised as 1 in its ca

Job Overview Acts as Lead Medical Writer on any type of writing project, including projects with multiple deliverables/components. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs senior review of all types of medical writing deliverables. Provides feedback and guidance to more junior st

Senior Consultant and Statistician, Patient-Centered Research Overview At IQVIA, the Patient Centered Solutions team helps clients generate robust evidence on the patient experience across clinical development, regulatory submissions, and scientific dissemination. Our Statistics & Psychometrics team specializes in the analysis of clinical outcome assessment (COA) and patient-reported outcomes (PRO

Purpose The Investigator Payments Analyst is accountable for budget planning, analytics and payment execution in a direct country or extended country group (OPC and satellite countries) in close collaboration with the SSO Study Start-Up Managers, SSO Clinical Project Managers and SSO Contracting Specialists in compliance with GCP/ICH, and regulatory requirements. Accountabilities Supports country

Location: Remote (UK, Spain, Soutch Africa, Hungary, Ireland, Italy, Portugal, Czech Republic, Bulgaria, Belgium) Role Overview: This unique role within IQVIA lends itself to a technically minded person with strong communication skills and SDTM knowledge. Having experience with SAS programming will be key for this position. The role can be based remotely from anywhere in Europe or in South Africa.

Step into a role where strategy meets impact. As a Clinical Supply Chain Manager , you will shape and drive the end-to-end supply strategy for new clinical trials. Using your ability to translate complex study protocols into smart kit designs and robust supply plans, you'll ensure that every element is aligned for seamless study execution. In this key position, you'll collaborate closely with inte

Step into a role where strategy meets impact. As a Clinical Supply Chain Manager , you will shape and drive the end‑to‑end supply strategy for new clinical trials. Using your ability to translate complex study protocols into smart kit designs and robust supply plans, you’ll ensure that every element is aligned for seamless study execution. In this key position, you’ll collaborate closely with inte

Job Overview Location: home-based, UK Accountable for capability and learning activities related to the delivery of CDGM services and the adoption of TMF and good documentation practices across the business. Responsibilities Develop and implement effective, fit-for-purpose capability development, learning, and knowledge management deliverables to users of TMF and CDGM services across the business.

Medical Science Liaison - Nutrition (Paediatric Allergy & Adult Enteral) 6-month contract - NATIONAL Nestlé Health Science is seeking an experienced Medical Science Liaison (MSL) to support its Nutrition portfolio , with a focus on Paediatric Allergy and Adult Enteral Nutrition , on a 6-month contract . This is a scientifically led, field-based role, working closely with healthcare professionals a

Job Overview _Location: home-based, UK_ Accountable for capability and learning activities related to the delivery of CDGM services and the adoption of TMF and good documentation practices across the business. Responsibilities Develop and implement effective, fit-for-purpose capability development, learning, and knowledge management deliverables to users of TMF and CDGM services across the busine

Medical Science Liaison - Nutrition (Paediatric Allergy & Adult Enteral) 6-month contract - NATIONAL Nestlé Health Science is seeking an experienced Medical Science Liaison (MSL) to support its Nutrition portfolio , with a focus on Paediatric Allergy and Adult Enteral Nutrition , on a 6-month contract . This is a scientifically led, field-based role, working closely with healthcare professionals a

RESPONSIBILITIES Serve as primary point of contact for customer on data management deliverables Manage multiple large studies or program of studies (possibly global) Provide leadership and senior support to DTLs on multiple large global programs of global studies Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage conti

The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning,executing, and reporting, (from first site initiation visit to and including study site close-out), of assigned studies in compliance with Sponsor processes and regulatory requirements. The CPM is the single point of contact and study team lead, in the country/cluster/hub, for the assigned studies. The CPM is respons

At IQVIA, we help improve healthcare and patient outcomes through knowledge, insight, and collaboration. Within our Interface business, our Medical Affairs team plays a key role in ensuring that clinical services delivered to healthcare professionals are designed and delivered to the highest ethical, regulatory, and quality standards. We are looking for a Medical Affairs Pharmacist to join our tea

RESPONSIBILITIES Serve as primary point of contact for customer on data management deliverables Manage multiple large studies or program of studies (possibly global) Provide leadership and senior support to DTLs on multiple large global programs of global studies Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage c

Associate Principal, Implementation Science & Mixed Methods Research IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. Patient Centered Solutions

The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning,executing, and reporting, (from first site initiation visit to and including study site close-out), of assigned studies in compliance with Sponsor processes and regulatory requirements. The CPM is the single point of contact and study team lead, in the country/cluster/hub, for the assigned studies. The CPM is respons

Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews. Lead statistical

Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews. Lead statistical s

As a Principal Biostatistician , you will provide end-to-end statistical leadership and integration support across Phase II and Phase III studies , working closely with cross-functional stakeholders in a fast-paced, global environment. Key Responsibilities - Provide Principal-level Biostatistics support for Phase II-III clinical trials - Independently lead SAP authoring and review - Support integr

Clinical Pharmacist Type : Full-time, hybrid We are looking for pharmacists to join the team to work across GP practices across south Wales and/ or the South West fo England Join us in this exciting role where you will utilise your clinical expertise and commercial acumen to support patients with chronic conditions in primary care settings. As a clinical pharmacist at Interface Clinical Services,

Job Overview The Associate Medical Director / Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities. Essential Function

Are you an experienced nurse with expertise in womens health? Do you excel in providing high-quality women's health services, including the fitting and removal of coils in a supportive and professional primary care environment? If so, we'd love to hear from you! We are seeking a passionate and skilled Women's Health Specialist Nurse to join our Healthcare Professionals Network in Carlisle. Key Res

Job Overview Acts as Lead Medical Writer on any type of writing project, including projects with multiple deliverables/components. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs senior review of all types of medical writing deliverables. Provides feedback and guidance to more junior st

Are you an experienced nurse with expertise in womens health? Do you excel in providing high-quality women's health services, including the fitting and removal of coils in a supportive and professional primary care environment? If so, we’d love to hear from you! We are seeking a passionate and skilled Women's Health Specialist Nurse to join our Healthcare Professionals Network in Carlisle. Key Res

Job Overview Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. Position may be responsible for the implementation of smaller programs in their entirety. Communicate with sponsors and project teams to implement and monitor impact of the recruitment/retent

Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Senior Clinical Research Associates in the UK. Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Func

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s Site Management (multi-sponsor) team is growing and seeking experienced Clinical Research Associates. We are recognised as a 2026 "Glassdoor Best Place to Work in the UK" and 1 in our category on the 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!). Apply today and forge a caree

Support CSC team members and Business Operations Management in the following trial specific activities: Quality Reviews, virtual trial master file uploads, document routing, study close-outs, reconciliation reports, data collection, change management, and various CSC related activities. Responsabilities and Tasks: Work in a team environment to select and complete various CSC related tasks from a c

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA are seeking experienced Clinical Research Associates in South West England to strengthen our cFSP sponsor-dedicated team. Why IQVIA? We share a passion for the work we do, and the impact it has on customers and patients. We are innovative, curious, and feel empowered to explore new ideas and ways of working. We collabo

Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. Why IQVIA? IQVIA is recognized as 1 in its category on the 2025 Fortune® World’s Most Admired Companies™ list for the FOURTH consecutive year! We offer genuine career development opportunities for those who want to grow as part of the organization. The c

Job Overview Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. Position may be responsible for the implementation of smaller programs in their entirety. Communicate with sponsors and project teams to implement and monitor impact of the recruitment/retent

Join IQVIA on our mission to accelerate innovation for a healthier world IQVIA UK's Site Management (multi-sponsor) team is growing and seeking experienced Clinical Research Associates. We are recognised as a 2026 "Glassdoor Best Place to Work in the UK" and 1 in our category on the 2026 Fortune® World's Most Admired Companies list (for the FIFTH consecutive year!). Apply today and forge a career

Senior eCOA Designer Location: UK, home-based Job Overview Provides technical and domain expertise in developing, delivering and supporting eCOA business systems to provide new or enhanced solutions to clients. Essential Functions - Under general direction, formulates and defines systems scope and objectives based on both user needs and a good understanding of applicable business systems and requi

Support CSC team members and Business Operations Management in the following trial specific activities: Quality Reviews, virtual trial master file uploads, document routing, study close-outs, reconciliation reports, data collection, change management, and various CSC related activities. Responsabilities and Tasks: Work in a team environment to select and complete various CSC related tasks from a

Join IQVIA on our mission to accelerate innovation for a healthier world IQVIA are seeking experienced Clinical Research Associates in South West England to strengthen our cFSP sponsor-dedicated team. Why IQVIA? We share a passion for the work we do, and the impact it has on customers and patients. We are innovative, curious, and feel empowered to explore new ideas and ways of working. We colla

Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. Why IQVIA? IQVIA is recognized as 1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year! We offer genuine career development opportunities for those who want to grow as part of the organization. The

Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Senior Clinical Research Associates in the UK. Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Func

Senior eCOA Designer Location: UK, home-based Job Overview Provides technical and domain expertise in developing, delivering and supporting eCOA business systems to provide new or enhanced solutions to clients. Essential Functions • Under general direction, formulates and defines systems scope and objectives based on both user needs and a good understanding of applicable business systems and requi

Job Overview Senior Global Trial Managers (SGTMs) are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The SGTM is a member of the core project team responsible for clinical delivery of large, multi-regional studies to meet contractual requirements and in accordance with (Standard Operat

Global Trial Delivery Manager services provide for the global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure global clinical operations deliverables progress according to agreed upon timelines and milestones, including country & site feasibility and site selection, trial set-up, tr

The Trial Delivery Leader (TDL) serves as the single point of accountability for trial operational strategy, trial-level budget, quality, and on-time delivery of assigned clinical trials. This role represents the evolution of the Global Trial Leader (GTL) , with a stronger emphasis on strategic leadership, end-to-end accountability, and governance-level decision making. The TDL works in close part

Job Overview Senior Global Trial Managers (SGTMs) are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients’ lives by bringing new drugs to the market faster. The SGTM is a member of the core project team responsible for clinical delivery of large, multi-regional studies to meet contractual requirements and in accordance with (Standard Operat

Bank Nurse needed in London Qualification: Nursing and in date NMC Pin plus experience in urinary catheterisation and ideally a specialism in urology Join the IQVIA Healthcare Professionals Network Today! Are you an experienced Nurse looking for additional bank shifts? IQVIA is seeking skilled nurses to join our Healthcare Professionals Network and support bank work opportunities in London. What W

The Trial Delivery Leader (TDL) serves as the single point of accountability for trial operational strategy, trial-level budget, quality, and on-time delivery of assigned clinical trials. This role represents the evolution of the Global Trial Leader (GTL) , with a stronger emphasis on strategic leadership, end-to-end accountability, and governance-level decision making. The TDL works in close part

Global Trial Delivery Manager services provide for the global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure global clinical operations deliverables progress according to agreed upon timelines and milestones, including country & site feasibility and site selection, trial set-up, tr

Associate Regulatory & Start-Up Manager Clinical Operations | Regulatory & Site Activation Location: Flexible / office-based depending on project needs Travel: Occasional travel may be required Contract Length: 4-6 months Are you looking to take the next step in your Regulatory & Start-Up career within clinical research? We are seeking an Associate Regulatory & Start-Up Manager to support and deli

Job Overview Lead and support effective corrective and preventive action (CAPA) management for significant quality issues (QIs) and audit and inspection responses including the assessment and review of investigations, appropriate root cause analysis and corrective and preventative actions. Provide support to management with insights, analyses and assessment and promotion of compliance with regulat

Regulatory & Start-Up Manager Clinical Operations | Regulatory & Site Activation Location: Flexible / office-based depending on project needs Travel: Occasional travel may be required Contract Length : 4- 6 months Are you an experienced Regulatory & Start-Up professional looking to lead complex clinical trial start-up activities across global or multi-regional studies? We are seeking a Regulatory

Join a sponsor-dedicated team and contribute to the advancement of in-house study activities over time. As the R Programming Lead , you will provide technical expertise to the Statistical Programming team, ensuring the delivery of high-quality solutions that meet both internal and external requirements. Responsibilities • Develop internal and external R packages for clinical trial analysis ( ADaM,

Job Overview Lead and support effective corrective and preventive action (CAPA) management for significant quality issues (QIs) and audit and inspection responses including the assessment and review of investigations, appropriate root cause analysis and corrective and preventative actions. Provide support to management with insights, analyses and assessment and promotion of compliance with regulat

Associate Regulatory & Start‑Up Manager Clinical Operations | Regulatory & Site Activation Location: Flexible / office‑based depending on project needs Travel: Occasional travel may be required Contract Length: 4-6 months Are you looking to take the next step in your Regulatory & Start‑Up career within clinical research? We are seeking an Associate Regulatory & Start‑Up Manager to support and deli

Regulatory & Start‑Up Manager Clinical Operations | Regulatory & Site Activation Location: Flexible / office‑based depending on project needs Travel: Occasional travel may be required Contract Length : 4- 6 months Are you an experienced Regulatory & Start‑Up professional looking to lead complex clinical trial start‑up activities across global or multi‑regional studies? We are seeking a Regulatory

Join IQVIA on our mission to accelerate innovation for a healthier world IQVIA UK's Site Management (multi-sponsor) team are seeking experienced Clinical Research Associates. We are recognised as a 2026 "Glassdoor Best Place to Work in the UK" and 1 in our category on the 2026 Fortune® World's Most Admired Companies list (for the FIFTH consecutive year!). Apply today and forge a career with greate

Global Clinical Project Manager - Vendor Management Expert – Single Sponsor Are you an experienced Vendor Management professional looking to make an impact in global clinical trials? We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Single Sponsor Department . In this role, you 'll become an expert in Vendor Management for global clinical trials across all pha

The Clinical Project Manager provides input to the overall operational trial(s) implementation, manages trial(s) timelines, budget, feasibility, country identification and sites selection, enhanced patient recruitment, and functions as the primary liaison for internal stakeholders and vendors. Funtions : Accountable to deliver Trial(s) on time, within budget, and with highest achievable quality.

Global Clinical Project Manager - Vendor Management Expert - Single Sponsor Are you an experienced Vendor Management professional looking to make an impact in global clinical trials? We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Single Sponsor Department . In this role, you 'll become an expert in Vendor Management for global clinical trials across all pha

Job Overview Acts as Lead Medical Writer on any type of writing project, including projects with multiple deliverables/components. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. Performs senior review of all types of medical writing deliverables. Provides feedback and guidance to more junior st

Hospital Sales Representative Full Time, Permanent role Therapy area: Paediatric Enteral Feeds IQVIA have an exciting opportunity in the East of England and are looking for experienced primary and secondary care specialists to work in a very rewarding environment with a great product portfolio. In this rewarding role, you will work with paediatric consultants and dietitians in hospitals, and some

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