59 Clinical Management jobs in the United Kingdom
Clinical Data Management Lead
Reading, South East
IQVIA
Posted 10 days ago
Job Viewed
Job Description
**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 continuous process improvements, issue escalation, workload projections, and provide technical expertise
+ Lead direct negotiations with customer, e.g., timelines, financial, process, resources
+ Meet with Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables
+ Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects
+ Serve as the escalation point for unresolved data issues
+ Ensure appropriate resources are assigned to meet project deliverables
+ Create and/or review and sign-off on all data management plan (DMP) documents
+ Manage service performance and provide leadership to identify root causes of issues and implement remedial actions
+ Serve as Subject Matter Expert (SME)
+ Provide leadership and expertise in a specific CDM task or technology
+ Independently manage SOW/budget
+ Independently bring process improvements and solutions to the CDM team/CDM department
+ Lead a focus team or global or local best practice team
+ Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
+ Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients)
+ Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation)
+ Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently
+ Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology
+ Knowledge of operating procedures and work instructions and the ability to apply them in practice
+ Knowledge of Good Clinical Practices and relevant regulatory guidelines
+ Excellent communication, interpersonal, customer service, and teamwork skills
+ Excellent organizational and problem-solving skills
+ Excellent project management skills
+ Ability to work independently
+ Comprehensive understanding of clinical drug development process
+ Ability to establish and maintain effective working relationships with co-workers, managers and customers
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
+ Bachelor's Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field
+ Around 7 years direct Data Management experience, including 5 or more years as a CDM project lead; or equivalent combination of education, training and experience
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
+ 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 continuous process improvements, issue escalation, workload projections, and provide technical expertise
+ Lead direct negotiations with customer, e.g., timelines, financial, process, resources
+ Meet with Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables
+ Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects
+ Serve as the escalation point for unresolved data issues
+ Ensure appropriate resources are assigned to meet project deliverables
+ Create and/or review and sign-off on all data management plan (DMP) documents
+ Manage service performance and provide leadership to identify root causes of issues and implement remedial actions
+ Serve as Subject Matter Expert (SME)
+ Provide leadership and expertise in a specific CDM task or technology
+ Independently manage SOW/budget
+ Independently bring process improvements and solutions to the CDM team/CDM department
+ Lead a focus team or global or local best practice team
+ Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
+ Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients)
+ Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation)
+ Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently
+ Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology
+ Knowledge of operating procedures and work instructions and the ability to apply them in practice
+ Knowledge of Good Clinical Practices and relevant regulatory guidelines
+ Excellent communication, interpersonal, customer service, and teamwork skills
+ Excellent organizational and problem-solving skills
+ Excellent project management skills
+ Ability to work independently
+ Comprehensive understanding of clinical drug development process
+ Ability to establish and maintain effective working relationships with co-workers, managers and customers
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
+ Bachelor's Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field
+ Around 7 years direct Data Management experience, including 5 or more years as a CDM project lead; or equivalent combination of education, training and experience
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
0
Specialist Clinical Waste Management Technician
BS1 3AG Bristol, South West
£30000 Annually
WhatJobs
Posted 19 days ago
Job Viewed
Job Description
Our client is seeking a highly dedicated and meticulous Specialist Clinical Waste Management Technician to join their vital, fully remote operations team. This role is essential for ensuring the safe, compliant, and efficient handling and disposal of clinical waste streams generated by healthcare facilities across the UK. You will be responsible for overseeing waste management processes remotely, providing expert guidance on segregation, containment, transportation, and disposal regulations, and ensuring adherence to all relevant legal frameworks and environmental standards. This is a critical role in public health and environmental protection.
Key responsibilities:
The ideal candidate will possess extensive knowledge of clinical waste management procedures, regulations, and best practices. Experience in a similar role within the healthcare, environmental services, or waste management sector is crucial. Excellent understanding of relevant legislation and health and safety requirements is essential. Strong analytical, problem-solving, and communication skills are required to provide effective remote support and guidance. The ability to work autonomously, manage multiple tasks, and maintain meticulous records is paramount. A relevant qualification in environmental health, waste management, or a related field is highly desirable. This role is fully remote, requiring a self-motivated individual with a strong work ethic and the ability to contribute effectively from their home office. While the role is remote, it supports operations connected to the Bristol, South West England, UK area.
Key responsibilities:
- Providing remote expert advice and support on all aspects of clinical waste management to a diverse range of healthcare providers.
- Developing and implementing robust waste management protocols and Standard Operating Procedures (SOPs) tailored to client needs.
- Ensuring compliance with stringent regulations, including the Hazardous Waste Regulations, Department of Health guidelines, and environmental protection laws.
- Conducting virtual audits and risk assessments of client waste management practices.
- Investigating and resolving any issues related to clinical waste handling, storage, or disposal.
- Training client staff remotely on best practices for waste segregation, labeling, and containment.
- Liaising with waste disposal contractors and regulatory bodies to ensure seamless operations.
- Maintaining detailed records of waste streams, disposal manifests, and compliance documentation.
- Advising on waste minimization strategies and promoting sustainable waste management practices.
- Staying updated on evolving legislation, technologies, and best practices in clinical waste management.
The ideal candidate will possess extensive knowledge of clinical waste management procedures, regulations, and best practices. Experience in a similar role within the healthcare, environmental services, or waste management sector is crucial. Excellent understanding of relevant legislation and health and safety requirements is essential. Strong analytical, problem-solving, and communication skills are required to provide effective remote support and guidance. The ability to work autonomously, manage multiple tasks, and maintain meticulous records is paramount. A relevant qualification in environmental health, waste management, or a related field is highly desirable. This role is fully remote, requiring a self-motivated individual with a strong work ethic and the ability to contribute effectively from their home office. While the role is remote, it supports operations connected to the Bristol, South West England, UK area.
This advertiser has chosen not to accept applicants from your region.
1
Senior Engineer Enabling Analytics & System Excellence (Clinical Trial Management Solutions)
High Wycombe, South East
J&J Family of Companies
Posted 1 day ago
Job Viewed
Job 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 are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
R&D Product Development
**Job Sub** **Function:**
R&D Digital
**Job Category:**
Scientific/Technology
**All Job Posting Locations:**
High Wycombe, Buckinghamshire, United Kingdom
**Job Description:**
**Senior Engineer, Enabling Analytics & System Excellence (Clinical Trial Management Solutions)**
**About Innovative Medicine:**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at are searching for the best talent for a Senior Engineer, Enabling Analytics & System Excellence (Clinical Trial Management Solutions)** **to be located in High Wycombe, United Kingdom or Beerse, Belgium (Hybrid).**
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
**High Wycombe, UK -** Requisition Number: R-
**Beerse, Belgium** - Requisition Number: R-
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
**Purpose:**
The Senior Engineer, Enabling Analytics & System Excellence (Clinical Trial Management Solutions) will provide expertise in the planning, administration and oversight of clinical systems and related processes administered by EASE within Clinical Trial Management Solutions (CTM Solutions) or Investigator & Patient Solutions (I&PS).
+ Provides support for capabilities related to clinical trial document management/TMF, study management and oversight.
+ Provides support for capabilities related to patient engagement & recruitment, site staff enablement, clinical staff training and digital health enablement.
Under general direction, this role executes plans and processes that innovate product development, meet organization standards, and follow digital strategy. This role is a liaison between the business community and key partners and stakeholders.
Senior Engineer, Enabling Analytics & System Excellence (Clinical Trial Management Solutions) plays a pivotal role in enhancing organizational capabilities, optimizing processes, and fostering collaboration to drive strategy, efficiency and quality across J&J systems and development initiatives.
**You will be responsible for** **:**
+ Leads the identification and implementation of technology solutions designed to optimize processes and deliver measurable value
+ Collaborates with clinical trial teams to assess their needs, exploring opportunities for innovation and continuous improvement through design thinking and agile methodologies
+ Work with study teams and partners on the study build, maintenance and use of supported systems during the lifecycle of a study
+ Provide end user support and expertise via support ticket intake, mailbox inquiries or other mechanisms
+ Serves as a point of contact for onboarding new organizations/acquisitions/divestitures related to study data/document transfer within scope of I&PS or CTM Solutions
+ Coordinate System release management activities including UAT testing and system improvements, and development/maintenance of system integrations including partnerships with IT and system owners
+ Troubleshoots advanced system issues, working with IT and external vendors to resolve challenges and ensure the continuous operation of supported capabilities.
+ Create / update training materials and reference documentation to support end users, and present to user community groups to drive usage and compliant use of systems
+ Lead team meetings, manage projects and participate in cross-functional projects
+ Collaborate with Subject Matter Experts, Process Owners, and Functional Management to ensure alignment with timelines, organizational SOPs, and regulatory requirements
+ Responsible for development and monitoring of metrics dashboards
+ Lead audit / inspection activities, including CAPA management
+ Sponsor external resources and serve as mentor to more junior internal resources
+ May serve as Owner for CTM Solution or I&PS capabilities
+ Represent on organizational initiatives
**Qualifications / Requirements:**
**Education:**
+ Minimum of a Bachelor's degree is required (preferably in Health, Science, Information Technology or another relevant field)
**Required:**
+ Minimum of 4-6 years of relevant experience in clinical trial execution with a Pharmaceutical, Medical Device company and/or a Clinical Research Organization (CRO)
+ Experience working with IT systems and related processes that support clinical development, reporting tools, Office 365 applications, and database administration
+ Knowledge of the drug development process, including Good Clinical Practices (GCPs) and FDA Code of Federal Regulations
+ The ability to partner with stakeholders and influence decision-making across a matrix organization
+ Excellent analytical, problem solving, communication and presentation skills
+ Global business mindset
+ Ability to travel up to 10% of the time (Domestic/International)
**Preferred:**
+ Experience with direct support of IT systems and related processes that support clinical development
+ Project Management or Process Improvement certification
+ Demonstrated ability to translate the use of technology to be applied to solving business problems and/or to improve business outcomes
**Benefits:**
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via , internal employees contact AskGS to be directed to your accommodation resource.
#LI-Hybrid
R&D Product Development
**Job Sub** **Function:**
R&D Digital
**Job Category:**
Scientific/Technology
**All Job Posting Locations:**
High Wycombe, Buckinghamshire, United Kingdom
**Job Description:**
**Senior Engineer, Enabling Analytics & System Excellence (Clinical Trial Management Solutions)**
**About Innovative Medicine:**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at are searching for the best talent for a Senior Engineer, Enabling Analytics & System Excellence (Clinical Trial Management Solutions)** **to be located in High Wycombe, United Kingdom or Beerse, Belgium (Hybrid).**
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
**High Wycombe, UK -** Requisition Number: R-
**Beerse, Belgium** - Requisition Number: R-
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
**Purpose:**
The Senior Engineer, Enabling Analytics & System Excellence (Clinical Trial Management Solutions) will provide expertise in the planning, administration and oversight of clinical systems and related processes administered by EASE within Clinical Trial Management Solutions (CTM Solutions) or Investigator & Patient Solutions (I&PS).
+ Provides support for capabilities related to clinical trial document management/TMF, study management and oversight.
+ Provides support for capabilities related to patient engagement & recruitment, site staff enablement, clinical staff training and digital health enablement.
Under general direction, this role executes plans and processes that innovate product development, meet organization standards, and follow digital strategy. This role is a liaison between the business community and key partners and stakeholders.
Senior Engineer, Enabling Analytics & System Excellence (Clinical Trial Management Solutions) plays a pivotal role in enhancing organizational capabilities, optimizing processes, and fostering collaboration to drive strategy, efficiency and quality across J&J systems and development initiatives.
**You will be responsible for** **:**
+ Leads the identification and implementation of technology solutions designed to optimize processes and deliver measurable value
+ Collaborates with clinical trial teams to assess their needs, exploring opportunities for innovation and continuous improvement through design thinking and agile methodologies
+ Work with study teams and partners on the study build, maintenance and use of supported systems during the lifecycle of a study
+ Provide end user support and expertise via support ticket intake, mailbox inquiries or other mechanisms
+ Serves as a point of contact for onboarding new organizations/acquisitions/divestitures related to study data/document transfer within scope of I&PS or CTM Solutions
+ Coordinate System release management activities including UAT testing and system improvements, and development/maintenance of system integrations including partnerships with IT and system owners
+ Troubleshoots advanced system issues, working with IT and external vendors to resolve challenges and ensure the continuous operation of supported capabilities.
+ Create / update training materials and reference documentation to support end users, and present to user community groups to drive usage and compliant use of systems
+ Lead team meetings, manage projects and participate in cross-functional projects
+ Collaborate with Subject Matter Experts, Process Owners, and Functional Management to ensure alignment with timelines, organizational SOPs, and regulatory requirements
+ Responsible for development and monitoring of metrics dashboards
+ Lead audit / inspection activities, including CAPA management
+ Sponsor external resources and serve as mentor to more junior internal resources
+ May serve as Owner for CTM Solution or I&PS capabilities
+ Represent on organizational initiatives
**Qualifications / Requirements:**
**Education:**
+ Minimum of a Bachelor's degree is required (preferably in Health, Science, Information Technology or another relevant field)
**Required:**
+ Minimum of 4-6 years of relevant experience in clinical trial execution with a Pharmaceutical, Medical Device company and/or a Clinical Research Organization (CRO)
+ Experience working with IT systems and related processes that support clinical development, reporting tools, Office 365 applications, and database administration
+ Knowledge of the drug development process, including Good Clinical Practices (GCPs) and FDA Code of Federal Regulations
+ The ability to partner with stakeholders and influence decision-making across a matrix organization
+ Excellent analytical, problem solving, communication and presentation skills
+ Global business mindset
+ Ability to travel up to 10% of the time (Domestic/International)
**Preferred:**
+ Experience with direct support of IT systems and related processes that support clinical development
+ Project Management or Process Improvement certification
+ Demonstrated ability to translate the use of technology to be applied to solving business problems and/or to improve business outcomes
**Benefits:**
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via , internal employees contact AskGS to be directed to your accommodation resource.
#LI-Hybrid
This advertiser has chosen not to accept applicants from your region.
2
Clinical Specialist Cardiac Rhythm Management - Central region UK
Solihull, West Midlands
Abbott
Posted 10 days ago
Job Viewed
Job Description
We are recruiting for a **Clinical Specialist** to join our Central UK team, responsible for supporting the **Cardiac Rhythm Management** (CRM) technology lines by providing expert clinical consultation, teaching and support on the use of the CRM portfolio of products and its appropriate application in the clinical setting in the assigned territory (Central UK team).
You will maintain up to date technical CRM knowledge of current and new Abbott therapies and technologies as well as a general understanding of the dynamics of the country healthcare market. You will provide technical support and assistance to the sales force, physicians and allied professionals for CRM case support.
You will be able to analyze the technical characteristics of competitors' devices and products, promote the CRM product lines and assist with market penetration by providing expert technical customer support.
What you'll need:
+ A science related degree.
+ Ideally experience within pacing/CRM and familiarity with cath lab procedures and protocol, but open to hearing from passionate graduates with a relevant degree looking for their first role in industry.
+ Strong communication skills.
+ A willingness to travel (c. 75% of the time).
As you'd expect from a global healthcare company, we offer a fantastic range of benefits to support you and your family, including competitive salaries and bonus potential, a superb defined contribution pension scheme, private healthcare, life assurance and a flexible benefits scheme.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
You will maintain up to date technical CRM knowledge of current and new Abbott therapies and technologies as well as a general understanding of the dynamics of the country healthcare market. You will provide technical support and assistance to the sales force, physicians and allied professionals for CRM case support.
You will be able to analyze the technical characteristics of competitors' devices and products, promote the CRM product lines and assist with market penetration by providing expert technical customer support.
What you'll need:
+ A science related degree.
+ Ideally experience within pacing/CRM and familiarity with cath lab procedures and protocol, but open to hearing from passionate graduates with a relevant degree looking for their first role in industry.
+ Strong communication skills.
+ A willingness to travel (c. 75% of the time).
As you'd expect from a global healthcare company, we offer a fantastic range of benefits to support you and your family, including competitive salaries and bonus potential, a superb defined contribution pension scheme, private healthcare, life assurance and a flexible benefits scheme.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
This advertiser has chosen not to accept applicants from your region.
3
Global Clinical Project Manager - Vendor Management Expert - Novartis Dedicated (home-based in Eu...
RG1 8JP Reading, South East
IQVIA
Posted today
Job Viewed
Job Description
Global Clinical Project Manager - Vendor Management Expert – Single Sponsor (Novartis)
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 , dedicated exclusively to Novartis . In this role, you 'll become an expert in Vendor Management for global clinical trials across all phases (Phase I–IV), ensuring seamless execution from study start-up through close-out.
What We’re Looking For
To excel in this role, you should bring:
- Global Clinical Project Management experience
- Strong Vendor Management expertise: Central lab, eCOA, IRT, ECG, Imaging, Ancillaries and/or Patient Recruitment & Retention with experience in global clinical trials. (must have experience managing at least 2 of these vendors)
- Deep understanding of clinical operations processes and vendor service categories.
- Excellent project management skills to drive efficiency and collaboration
- Strong communication and influencing abilities to partner effectively across functions.
- Proven ability to manage risk and performance issues in a fast-paced environment
What You’ll Do
As a Global Clinical Project Manager - Vendor Management Expert , you will be responsible for ensuring vendor deliverables are met with quality and efficiency at the trial level. Your key responsibilities include:
- Vendor Oversight & Coordination – Manage vendor activities across the study lifecycle, ensuring timely and high-quality deliverables.
- Study Start-Up Support – Oversee vendor deliverables during study initiation, ensuring smooth onboarding and activation.
- Risk & Performance Management – Track vendor performance, identify risks, and escalate issues as needed.
- Site Readiness & Activation – Drive vendor activities to support site activations and ensure study milestones are met.
- Study Close-Out – Coordinate vendor deliverables that support Database Lock and study closure.
What You’ll Deliver
- Vendor service excellence at the study level
- Vendor onboarding and performance tracking
- KPI (Key Performance Indicator) and KQI (Key Quality Indicator) dashboards to monitor vendor effectiveness
- Site readiness monitoring and documentation
- Risk mapping with contingency planning
- Vendor cost control and oversight
Please note this role is not eligible for the UK visa sponsorship.
This is an exciting opportunity to play a critical role in global clinical trials , ensuring vendor excellence and operational success. If you’re ready to take on a high-impact role with a leading sponsor, we’d love to hear from you!
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at
This advertiser has chosen not to accept applicants from your region.
4
Global Clinical Project Manager - Vendor Management Expert - Novartis Dedicated (home-based in Eu...
London, London
IQVIA
Posted 10 days ago
Job Viewed
Job Description
**Global Clinical Project Manager - Vendor Management Expert - Single Sponsor (Novartis)**
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** , dedicated exclusively to **Novartis** . In this role, you 'll become an expert in **Vendor Management** for global clinical trials across all phases (Phase I-IV), ensuring seamless execution from study start-up through close-out.
**What We're Looking For**
To excel in this role, you should bring:
+ **Global Clinical Project Management experience**
+ **Strong Vendor Management expertise:** Central lab, eCOA, IRT, ECG, Imaging, Ancillaries and/or Patient Recruitment & Retention with experience in global clinical trials. (must have experience managing at least 2 of these vendors)
+ **Deep understanding of clinical operations processes** and vendor service categories.
+ **Excellent project management skills** to drive efficiency and collaboration
+ **Strong communication and influencing abilities** to partner effectively across functions.
+ **Proven ability to manage risk and performance issues** in a fast-paced environment
**What You'll Do**
As a **Global Clinical Project Manager - Vendor Management Expert** , you will be responsible for ensuring vendor deliverables are met with **quality and efficiency** at the trial level. Your key responsibilities include:
+ **Vendor Oversight & Coordination** - Manage vendor activities across the study lifecycle, ensuring timely and high-quality deliverables.
+ **Study Start-Up Support** - Oversee vendor deliverables during study initiation, ensuring smooth onboarding and activation.
+ **Risk & Performance Management** - Track vendor performance, identify risks, and escalate issues as needed.
+ **Site Readiness & Activation** - Drive vendor activities to support site activations and ensure study milestones are met.
+ **Study Close-Out** - Coordinate vendor deliverables that support Database Lock and study closure.
**What You'll Deliver**
+ **Vendor service excellence at the study level**
+ **Vendor onboarding and performance tracking**
+ **KPI (Key Performance Indicator) and KQI (Key Quality Indicator) dashboards to monitor vendor effectiveness**
+ **Site readiness monitoring and documentation**
+ **Risk mapping with contingency planning**
+ **Vendor cost control and oversight**
**Please note this role is not eligible for the UK visa sponsorship.**
This is an exciting opportunity to play a **critical role in global clinical trials** , ensuring vendor excellence and operational success. If you're ready to take on a **high-impact role** with a leading sponsor, we'd love to hear from you!
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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** , dedicated exclusively to **Novartis** . In this role, you 'll become an expert in **Vendor Management** for global clinical trials across all phases (Phase I-IV), ensuring seamless execution from study start-up through close-out.
**What We're Looking For**
To excel in this role, you should bring:
+ **Global Clinical Project Management experience**
+ **Strong Vendor Management expertise:** Central lab, eCOA, IRT, ECG, Imaging, Ancillaries and/or Patient Recruitment & Retention with experience in global clinical trials. (must have experience managing at least 2 of these vendors)
+ **Deep understanding of clinical operations processes** and vendor service categories.
+ **Excellent project management skills** to drive efficiency and collaboration
+ **Strong communication and influencing abilities** to partner effectively across functions.
+ **Proven ability to manage risk and performance issues** in a fast-paced environment
**What You'll Do**
As a **Global Clinical Project Manager - Vendor Management Expert** , you will be responsible for ensuring vendor deliverables are met with **quality and efficiency** at the trial level. Your key responsibilities include:
+ **Vendor Oversight & Coordination** - Manage vendor activities across the study lifecycle, ensuring timely and high-quality deliverables.
+ **Study Start-Up Support** - Oversee vendor deliverables during study initiation, ensuring smooth onboarding and activation.
+ **Risk & Performance Management** - Track vendor performance, identify risks, and escalate issues as needed.
+ **Site Readiness & Activation** - Drive vendor activities to support site activations and ensure study milestones are met.
+ **Study Close-Out** - Coordinate vendor deliverables that support Database Lock and study closure.
**What You'll Deliver**
+ **Vendor service excellence at the study level**
+ **Vendor onboarding and performance tracking**
+ **KPI (Key Performance Indicator) and KQI (Key Quality Indicator) dashboards to monitor vendor effectiveness**
+ **Site readiness monitoring and documentation**
+ **Risk mapping with contingency planning**
+ **Vendor cost control and oversight**
**Please note this role is not eligible for the UK visa sponsorship.**
This is an exciting opportunity to play a **critical role in global clinical trials** , ensuring vendor excellence and operational success. If you're ready to take on a **high-impact role** with a leading sponsor, we'd love to hear from you!
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
5
Global Clinical Project Manager - Vendor Management Expert - Novartis Dedicated (home-based in Eu...
Reading, South East
IQVIA
Posted 10 days ago
Job Viewed
Job Description
**Global Clinical Project Manager - Vendor Management Expert - Single Sponsor (Novartis)**
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** , dedicated exclusively to **Novartis** . In this role, you 'll become an expert in **Vendor Management** for global clinical trials across all phases (Phase I-IV), ensuring seamless execution from study start-up through close-out.
**What We're Looking For**
To excel in this role, you should bring:
+ **Global Clinical Project Management experience**
+ **Strong Vendor Management expertise:** Central lab, eCOA, IRT, ECG, Imaging, Ancillaries and/or Patient Recruitment & Retention with experience in global clinical trials. (must have experience managing at least 2 of these vendors)
+ **Deep understanding of clinical operations processes** and vendor service categories.
+ **Excellent project management skills** to drive efficiency and collaboration
+ **Strong communication and influencing abilities** to partner effectively across functions.
+ **Proven ability to manage risk and performance issues** in a fast-paced environment
**What You'll Do**
As a **Global Clinical Project Manager - Vendor Management Expert** , you will be responsible for ensuring vendor deliverables are met with **quality and efficiency** at the trial level. Your key responsibilities include:
+ **Vendor Oversight & Coordination** - Manage vendor activities across the study lifecycle, ensuring timely and high-quality deliverables.
+ **Study Start-Up Support** - Oversee vendor deliverables during study initiation, ensuring smooth onboarding and activation.
+ **Risk & Performance Management** - Track vendor performance, identify risks, and escalate issues as needed.
+ **Site Readiness & Activation** - Drive vendor activities to support site activations and ensure study milestones are met.
+ **Study Close-Out** - Coordinate vendor deliverables that support Database Lock and study closure.
**What You'll Deliver**
+ **Vendor service excellence at the study level**
+ **Vendor onboarding and performance tracking**
+ **KPI (Key Performance Indicator) and KQI (Key Quality Indicator) dashboards to monitor vendor effectiveness**
+ **Site readiness monitoring and documentation**
+ **Risk mapping with contingency planning**
+ **Vendor cost control and oversight**
**Please note this role is not eligible for the UK visa sponsorship.**
This is an exciting opportunity to play a **critical role in global clinical trials** , ensuring vendor excellence and operational success. If you're ready to take on a **high-impact role** with a leading sponsor, we'd love to hear from you!
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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** , dedicated exclusively to **Novartis** . In this role, you 'll become an expert in **Vendor Management** for global clinical trials across all phases (Phase I-IV), ensuring seamless execution from study start-up through close-out.
**What We're Looking For**
To excel in this role, you should bring:
+ **Global Clinical Project Management experience**
+ **Strong Vendor Management expertise:** Central lab, eCOA, IRT, ECG, Imaging, Ancillaries and/or Patient Recruitment & Retention with experience in global clinical trials. (must have experience managing at least 2 of these vendors)
+ **Deep understanding of clinical operations processes** and vendor service categories.
+ **Excellent project management skills** to drive efficiency and collaboration
+ **Strong communication and influencing abilities** to partner effectively across functions.
+ **Proven ability to manage risk and performance issues** in a fast-paced environment
**What You'll Do**
As a **Global Clinical Project Manager - Vendor Management Expert** , you will be responsible for ensuring vendor deliverables are met with **quality and efficiency** at the trial level. Your key responsibilities include:
+ **Vendor Oversight & Coordination** - Manage vendor activities across the study lifecycle, ensuring timely and high-quality deliverables.
+ **Study Start-Up Support** - Oversee vendor deliverables during study initiation, ensuring smooth onboarding and activation.
+ **Risk & Performance Management** - Track vendor performance, identify risks, and escalate issues as needed.
+ **Site Readiness & Activation** - Drive vendor activities to support site activations and ensure study milestones are met.
+ **Study Close-Out** - Coordinate vendor deliverables that support Database Lock and study closure.
**What You'll Deliver**
+ **Vendor service excellence at the study level**
+ **Vendor onboarding and performance tracking**
+ **KPI (Key Performance Indicator) and KQI (Key Quality Indicator) dashboards to monitor vendor effectiveness**
+ **Site readiness monitoring and documentation**
+ **Risk mapping with contingency planning**
+ **Vendor cost control and oversight**
**Please note this role is not eligible for the UK visa sponsorship.**
This is an exciting opportunity to play a **critical role in global clinical trials** , ensuring vendor excellence and operational success. If you're ready to take on a **high-impact role** with a leading sponsor, we'd love to hear from you!
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
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6
Clinical Operations Manager
Newcastle upon Tyne, North East
JAYCO Recruitment
Posted 12 days ago
Job Viewed
Job Description
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About the Company
Jayco Recruitment is proud to be representing one of the North East’s most respected and forward-thinking care providers in their search for a Clinical Operations Manager to oversee a portfolio of high-quality nursing homes. This is an exceptional opportunity for an experienced clinical leader who thrives on driving excellence in care, compliance, and operational performance across multiple sites.
About the Role
As Clinical Operations Manager, you will provide strategic and hands-on leadership to Home Managers and clinical teams, ensuring outstanding standards of nursing care and compliance with all CQC requirements. You’ll be instrumental in developing best practice, mentoring leadership teams, and embedding a culture of compassion, safety, and accountability across the group.
Responsibilities
- Overseeing clinical governance, auditing, and quality improvement across all homes.
- Supporting Home Managers with leadership, performance, and staff development.
- Monitoring and improving CQC outcomes, safeguarding processes, and care quality indicators.
- Driving excellence in clinical standards and person-centred care delivery.
- Liaising with local authorities, CCGs, and external regulators.
- Leading by example and fostering a positive, progressive culture throughout the group.
Qualifications
- Qualified Nurse (RGN/RMN/RNLD) with active NMC PIN.
- Proven multi-site management experience within elderly care or nursing homes.
- Strong knowledge of CQC frameworks and clinical governance.
- Excellent leadership, coaching, and communication skills.
- Full UK driving licence and flexibility to travel across the region.
Required Skills
- Qualified Nurse (RGN/RMN/RNLD) with active NMC PIN.
- Proven multi-site management experience within elderly care or nursing homes.
- Strong knowledge of CQC frameworks and clinical governance.
- Excellent leadership, coaching, and communication skills.
- Full UK driving licence and flexibility to travel across the region.
Preferred Skills
- Experience in driving clinical excellence across multiple sites.
- Ability to mentor and develop leadership teams.
Pay range and compensation package
Competitive salary based on experience.
Equal Opportunity Statement
We are committed to diversity and inclusivity in our hiring practices.
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7
Clinical Operations Manager
Leeds, Yorkshire and the Humber
Enable Therapy Services Ltd
Posted 12 days ago
Job Viewed
Job Description
Join Enable Therapy Services as Clinical Operations Manager
Shape the future of rehabilitation across the UK.
Enable Therapy Services (ETS) is seeking a dynamic and visionary Clinical Operations Manager to lead our nationwide clinical services. As the senior clinical voice within our Senior Management Team, you’ll drive strategic direction, uphold clinical excellence, and ensure our rehabilitation services remain responsive, high-quality, and sustainable.
️ What You’ll Lead
- Strategic development of clinical services in line with the Rehabilitation Code 2015
- Governance of assessments, treatment planning, and case management
- Performance oversight across SLAs, KPIs, and compliance standards
- Direct line management of the Head of Case Management and Clinical Support Lead
- Cross-functional collaboration with senior leaders to enhance service delivery
- External representation of ETS in clinical and commercial engagements
Why ETS? ETS is a trusted provider of rehabilitation services, known for innovation, integrity, and impact. You’ll be at the heart of shaping services that change lives—working with a passionate team and contributing to national healthcare transformation.
Who We’re Looking For
- NMC/HCPC-registered clinician (OT, OH, or Physiotherapy)
- Experience of Case Management in an Occupational Therapy role
- Proven leadership in clinical governance and operational management
- Strategic thinker with a passion for service development
- Strong communicator with a collaborative mindset
- Experience in remote team management and commercial healthcare is a plus
Ready to make a difference? If you’re a clinical leader ready to take the next step in your career, we’d love to hear from you. Join us in delivering excellence, driving innovation, and shaping the future of rehabilitation.
Apply now and lead with purpose at ETS.
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8
Clinical Operations Specialist
Unity Systems
Posted 1 day ago
Job Viewed
Job Description
Job Title: Contract Clinical Operations Lead (COL)
Location: Welwyn Garden City, Hertfordshire (Hybrid, 2+ days/week onsite)
Contract: 6 Months | Inside IR35
About the Role
As a Contract Clinical Operations Lead (COL) , you will play a key role in leading the operational delivery of global clinical trials across all phases. This position is part of the Global Clinical Operations function and contributes to the vision of delivering high-quality, patient-centric, and compliant studies.
This is an excellent opportunity for experienced clinical operations professionals looking to take on a strategic, cross-functional leadership role in a fast-paced and collaborative environment .
Key Responsibilities
- Develop and manage study operational plans , including timelines, resources, and budgets.
- Oversee vendor relationships and performance , ensuring alignment with project goals and quality standards.
- Provide leadership and operational oversight to global, cross-functional study teams.
- Ensure adherence to ICH/GCP and other relevant regulatory guidelines.
- Lead country feasibility, site selection, and site engagement activities.
- Manage clinical supply planning and resource forecasting .
- Act as the primary point of contact for internal and external stakeholders.
- Contribute to internal disease area and portfolio communities to drive operational excellence.
Required Qualifications & Experience
- Minimum 3 years’ experience in clinical trial operations or related roles.
- Bachelor’s degree in Life Sciences or equivalent professional experience.
- Strong understanding of the clinical development lifecycle and regulatory requirements .
- Proven ability to lead global or regional clinical studies in matrixed organizations.
- Excellent communication, collaboration, and stakeholder management skills.
- Highly proactive , adaptable, and results-driven with a focus on quality .
- Availability within 1 month preferred.
Preferred Skills
- Experience managing end-to-end global clinical studies .
- Demonstrated vendor oversight experience (CROs, central labs, or eCOA providers).
- Familiarity with digital clinical operations tools (e.g. Veeva, CTMS, Workday).
Additional Information
- Contractors will be assigned a Workday Manager and integrated into study delivery teams.
- Standard onboarding and equipment will be provided.
- Contractors are responsible for correcting any sub-standard work at their own cost and may end the assignment with notice.
Candidate Profile – Ideal Fit
- Experienced and adaptable Clinical Operations Lead with global trial delivery experience .
- Strong vendor and stakeholder management skills.
- Comfortable working in dynamic, fast-paced environments .
- Collaborative, quality-focused, and driven by operational excellence .
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