37 Clinical Management jobs in the United Kingdom
Lead Clinician
Job Viewed
Job Description
Are you looking for an employer who can offer you opportunities for growth and development in your clinical career- All whilst working within a friendly multidisciplinary team in a rewarding education setting?
Do you want to have opportunities to participate in research projects, special interest groups and form part of a wider clinical network that meets regularly for training & development?
Do you want to have flexibility and be able to work creatively to deliver specialist assessments and interventions fostering independence within an education setting?
Do you want to be part of developing an enhanced clinical offer through supporting the growth of colleagues, apprentices, students and therapy assistants?
How about working for an employer who has been awarded a ‘Great Place to Work’ for the 5th year running?
Does working 4 days a week with FULL pay sound like a dream!* It doesn't have to be! Have a better work/life balance and come and work for Outcomes First Group!
Job Title: Lead Clinician
Location: Avonside School – Bristol, BS4 5PS
Salary: £50,000 - £60,000 FTE DOE
Hours: 37.5 hours per week, Monday to Friday
Contract: Permanent (Term time only, or flexibility around full-time contract can be discussed based on your personal circumstances)
Essential: Full UK driving licence and access to own vehicle
In a world where the demand for clinical support is increasing daily, we understand the importance and value of the work you carry out. Your unique skills and expertise are critical to building better outcomes for our pupils. This is why we aim to have a multidisciplinary clinical team for each of our sites to provide this vital provision in collaboration with our education teams. Creating an environment where our pupils can truly flourish and grow in independence is key.
About the Group:
Outcomes First Group is the leading provider of world-class education. Our schools are a vital part of local communities in England, Scotland and Wales, with a renowned reputation for quality and positive outcomes for the children and young people we educate for. Our Acorn schools are there to meet the social and emotional needs of pupils who have faced trauma or adversity, equipping them for life’s important steps. Our Options Autism schools support autistic pupils to value their uniqueness and access the world in their own way. Another division, Momenta Connect, supports young people to overcome barriers and engage with education. While our most recent addition, Blenheim Schools, enables outstanding futures through high-quality independent and international schools.
Our Vision
Empower every child, whatever their ability, with a world-class education that nurtures potential, inspires lifelong learning, and equips them to thrive in a diverse and evolving world.
Our Mission
We commit to unlocking our pupils’ potential through personalised learning, innovation, and opportunity, supporting growth and aspirations.
Our Promise
- WE LISTEN. We never assume.
- WE WORK TOGETHER. To make the remarkable happen.
- WE ARE ACCOUNTABLE. To each other and for one another.
Our Promise describes the sort of people we are and our commitment to how we treat each other, work together and behave. It represents what’s truly important to us as individuals and as a team. It is easily translatable into behaviours we all practice and experience every day. It's the golden thread that runs through every leader, team and individual.
The role:
We are looking for a Lead Clinician to manage our in-house Clinical Team at Avonside School based in Bristol. The postholder will work collaboratively with both the school’s Senior Leadership Team (SLT) and the Regional Clinical Lead. The role will be split between clinically leading the team and holding a therapy caseload. Working collaboratively with the team, the postholder will deliver bespoke assessment and intervention plans for our students who may present with complex profiles of need as a result of autism and other types of neurodivergence, developmental trauma and social, emotional and mental health (SEMH) needs. Meeting the needs of EHCP plans will be a primary focus in this role, target led, via the OFG ‘all’, ‘group’ and ‘individual’ clinical ways of working, embedded into our clinical practice. They will also be responsible for coordinating the line management of the members of the onsite clinical team and leading on the service development of the clinical school-based service, alongside the school SLT and Regional Clinical Lead.
Our Clinical Teams help maintain a person-centred, empowering approach always putting the pupils we support at the forefront of everything they do. All our settings maintain a strong safeguarding culture, and the pupils we support are heard, respected, and involved in decisions that affect them. We strive for excellence, which is why we are one of the leading service providers in the UK. With this in mind, we are looking for a Lead Clinician who shares our vision to use innovative approaches to enhance the quality of life and outcomes of the pupils we support.
Location: Avonside School – Bristol, BS4 5PS – Avonside School f orms part of our Acorn Educations brand and is an independent specialist day school supporting young people aged 13 – 19
- Avonside School opening Winter 2025
- School Finder - Acorn
For further information regarding this vacancy please refer to the Job Description and Person Specification attached.
Essential Criteria:
- Degree or Masters in Speech and Language Therapy, Occupational Therapy, Psychotherapy or Doctorate in Psychology
- Experience within the specialist client group; working with autistic individuals and/or those with complex needs.
- Valid and up to date professional Registration & membership of professional body e.g. BPS
- Clear and concise report writing relating to clinical and research activities
- Experience of providing supervision and supporting a therapy team
- Ability to work independently
- Ability to work dynamically and within a growing and developing clinical service
- Experience of multi-professional work with teams or services within the designated specialty preferred
- Full UK valid driving licence and access to own vehicle
Why work for us?
Alongside working with a network of over 350 clinical colleagues with regular forums for peer reflection and practice development, Outcomes First Group offer an array of flexible benefit options:
Benefits
Your health and wellbeing are important to us, so you’ll get an exceptional reward and flexible benefits package including:
- Life Assurance
- Pension scheme with options to increase your contributions
- “Your Wellbeing Matters” – access to a wide range of first-class mental health support services and physical health checks
- *You’ll work 80% of your contractual hours for 100% of your pay, giving you more time to do the things that make you happy. 4DWW is subject to successful completion of probation and is not a contractual benefit
- Family Growth Support - inclusive benefits package covering enhanced maternity and paternity leave, along with paid fertility treatment support.
- A wide range of health, wellbeing, and insurance benefits
- 100’s of discount options valid in the UK and abroad
- Cycle to Work Schemes
- Electric Car Purchase Scheme
- Critical illness cover
At Outcomes First Group we are committed to the safeguarding and promoting the welfare of our pupils and young people. All successful applicants will be subject to social media checks and successful applicants to a fully enhanced DBS
We reserve the right to close vacancies early, please submit your application at the earliest opportunity.
Outcomes First Group is committed to carrying out a fair, thorough and efficient recruitment process in line with Keeping Children Safe in Education. Whilst we aim to keep applicants informed throughout, Outcomes First Group does not accept liability for any loss of earnings or other associated costs incurred by applicants as a result of delays or changes in the compliance process. All stages of the compliance process are subject to necessary safeguarding checks and compliance with statutory requirements, which may affect timescales.
Job Ref: 280657
#Leadclinician#Psychology#CareersinEducation#SpecialEducation#CareersinCare #CareersinSpecialEducation #Therapists
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Senior Operations Manager - Healthcare Administration
Posted 4 days ago
Job Viewed
Job Description
Key Responsibilities:
- Manage the day-to-day operations of administrative departments, including patient reception, scheduling, billing, and medical records.
- Develop and implement operational policies and procedures to enhance efficiency and service quality.
- Oversee staff scheduling, training, and performance management for administrative teams.
- Monitor and analyze operational performance metrics, identifying areas for improvement and implementing solutions.
- Ensure compliance with all healthcare regulations, data privacy laws (e.g., GDPR, HIPAA), and quality standards.
- Manage budgets for administrative departments, controlling costs and optimizing resource allocation.
- Liaise with medical staff, department heads, and external stakeholders to ensure seamless operations.
- Implement and manage IT systems and software related to healthcare administration.
- Lead projects focused on process improvement, cost reduction, and service enhancement.
- Maintain a high level of patient satisfaction through effective administrative support.
- Ensure a safe and compliant working environment for all administrative staff.
Qualifications:
- Bachelor's degree in Healthcare Administration, Business Administration, or a related field.
- Minimum of 6 years of experience in healthcare administration or operations management, with at least 3 years in a supervisory or managerial role.
- Proven track record in improving operational efficiency and implementing process improvements in a healthcare setting.
- In-depth knowledge of healthcare administrative processes, medical terminology, and billing procedures.
- Familiarity with healthcare regulations and compliance standards.
- Strong leadership, team management, and motivational skills.
- Excellent organizational, planning, and problem-solving abilities.
- Proficiency in using healthcare management software and MS Office Suite.
- Strong communication and interpersonal skills, with the ability to build relationships with diverse stakeholders.
- Master's degree in a relevant field or relevant professional certifications are a plus.
This role presents a significant opportunity for a seasoned administrator to drive operational excellence within a reputable healthcare organization.
Associate Vice President, Clinical Data Management
Posted 13 days ago
Job Viewed
Job Description
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
**ASSOCIATE VICE PRESIDENT, CLINICAL DATA MANAGEMENT**
**Live**
**What you will do**
The Associate Vice President, Clinical Data Management is a member of the Global Development Operations (GDO) leadership team and is a strategic partner to the R&D organization.
**You will lead Amgen's Clinical Data Management function within GDO, ensuring the highest quality of clinical data collection, processing, and analysis to support regulatory submissions and clinical development** **programs.** **This role is responsible for the strategic direction, leadership, and operational oversight of data management processes supporting clinical trials across all therapeutic areas and phases.**
You will collaborate closely with cross-functional teams including clinical operations, biostatistics, regulatory affairs, and quality to drive data integrity and compliance with global regulatory standards.
The role requires a visionary leader with deep expertise in CDM and a proven ability to scale and lead global teams in a complex matrix environment.
**Responsibilities:**
+ **Develop and drive the global data management strategy in alignment with clinical development objectives and corporate goals.**
+ **Provide strategic and operational leadership to the Clinical Data Management (CDM) function across all clinical programs and phases.**
+ **Lead innovation initiatives, including the implementation of development integration programs and the adoption of cutting-edge technologies to enhance data workflows.**
+ Represent Clinical Data Management in executive leadership discussions, regulatory interactions, and industry forums.
+ Establish and enforce robust clinical data governance models, policies, and risk mitigation strategies to ensure quality and compliance.
+ **Make final decisions regarding standard operating procedures (SOPs), CDM best practices, and process optimization.**
+ Engage key stakeholders and ensure timely resolution on critical data integrity and regulatory compliance issues.
+ Serve as the primary CDM representative during regulatory inspections and audits, with responsibility for final decisions on findings, responses, and corrective actions.
+ Influence cross-functional clinical development, operational, and regulatory strategies through data-driven insights and analytics.
+ Partner closely with Clinical Program Operations, Regulatory, Biostatistics, and R&D to ensure seamless integration and alignment of clinical data.
+ Build and maintain strategic relationships with CROs, vendors, regulatory authorities, and industry organizations to advance CDM excellence.
+ Influence internal leadership and functional partners to promote data-driven decision-making across clinical programs.
+ Lead audit readiness efforts and promote a culture of continuous improvement and compliance within the CDM function.
+ Implement protocols and tools to ensure data security, integrity, and risk management across all platforms and studies.
+ Optimize staffing, outsourcing strategies, and technology investments to improve cost-efficiency, scalability, and delivery timelines.
**Win**
**What we expect of you**
We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an experienced leader with the following qualifications.
**Basic Qualifications:**
+ **Degree educated in relevant discipline**
+ **Extensive data management experience including managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources**
**Preferred Qualifications:**
+ Experience within clinical data management, regulatory compliance, and strategic leadership within a pharmaceutical, biotech, or CRO environment.
+ **Expertise in GCP, ICH, FDA, EMA regulations, data governance, and clinical trial data standards (CDISC, SDTM).**
+ Experience within cross-functional collaborations, leadership, and strategic planning skills, ensuring operational excellence and compliance while driving innovation in data management to support Amgen's global clinical development efforts.
+ Expertise in AI/ML-driven data management solutions, automation, and advanced analytics.
+ **Understanding of clinical data standards (CDISC, SDTM, ADaM).**
+ **Experience leading regulatory submissions, including NDA/BLA/MAA filings and advisory committee interactions**
+ Proven ability to drive organizational change, optimize processes, and implement lean principles in clinical data management.
+ Cross-functional collaboration experience with clinical operations, regulatory affairs, biostatistics, and R&D teams.
+ **Experience managing FSP relationships and technology implementations (EDC, CTMS, RWD/RWE).**
+ **Knowledge of emerging trends in digital health, data governance, and data privacy regulations (GDPR, HIPAA).**
+ Familiarity with decentralized trial models and digital health technologies.
The successful candidate will also embody the Amgen leadership attributes which are:
+ **Inspire:** Create a connected, inclusive, and inspiring work environment that empowers talent to thrive
+ **Accelerate:** Enable speed that matches the urgency of patient needs by encouraging progress over perfection
+ **Integrate:** Connect the dots to amplify the collective power of Amgen to drive results for patients, staff, and shareholders
+ **Adapt:** Lead through change by adapting to an ever-changing environment and defining a clear course of action to deliver results
**Thrive**
**What you can expect of us**
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Manager, Global Submission Management, Clinical Trials
Posted today
Job Viewed
Job Description
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
**Position Purpose**
The Submission Manager, Clinical Trials manages and coordinates the timely, compliant, and accurate delivery of the core submission documents and dossiers to Bristol Myers Squibb (BMS) HA/EC Applicants and CRO. The Submission Manager also participates in the preparation of the CTIS for CT under the EU Regulation
**Key Responsibilities**
+ Prepare and distribute the global Clinical Trial Application dossier and subsequent substantial amendments to country applicants and CROs for submission to ECs and HAs.
+ Prepare the data required in CTIS for global Clinical Trial Application dossiers and their subsequent substantial modifications.
+ Manage the CT Amendment log considering the EU Regulation and determine windows of opportunity for submissions, escalate within BMS
+ Provide support to the Submission Senior Manager/collaborate with the Submission Specialist in CTA preparation activities for initial filings and start up activities, protocol amendments, end of trials and CSR distributions.
+ Ensure consistency of the Clinical Trial application across projects, studies and countries.
+ Lead Program/Study level CTA Tracking Meetings, in preparation of the CTA dossier, ensuring timelines and dossier quality are managed according to expectations.
+ Liaise with country offices and central team (Clinical Supply Operations, Operation Leads, Protocol Managers, Medical Monitor, Safety, Quality Person) to ensure that Clinical trial application activities are in compliance with study timelines, BMS SOPs, worldwide regulatory guidelines and regulations.
+ Comply with the use and maintenance of the available planning & tracking tools (e.g. Veeva - HA submission and approval Tracking system) to generate reports and track the CTA content and associated dates.
+ Escalate to study teams and GSM-CT senior roles observed trends and issues that may impact timely and successful study approval and execution
+ Contribute to the Global Country Requirements Repository by collecting and sharing additional country requirements.
+ Support initiatives for innovation and simplification in the processes to improve the support to the study teams and GSM-CT.
+ Coordinate updates within a Program.
+ Support continuous improvement and compliance initiatives
+ Utilizes technology effectively to support the clinical trial application submission process. Proficient use of CTMS, Tracking systems, Excel trackers, to generate reports and track the CTAp content and associated dates
+ Contributes to other requirements as appropriate to allow proper functioning of the GSM-CT.
+ Support implementation of the EU CT REG Portal from Feb 2022.
+ Provide training/mentoring to the GSM-CT newcomers
**Required Qualifications & Experience**
+ BA/BS degree in a science or technology field, preferred
+ Extensive relevant regulatory submissions experience
**Key Competencies**
+ Expert knowledge of Regulatory Submissions and package content for non-US clinical trial applications to health authorities.
+ Assists in the development of short- and long-term goals for own workgroup in alignment with those of GSM and the R&D umbrella.
+ Resolves problems/difficulties with the assistance of senior team members.
+ Supports other functions as appropriate.
+ Independently facilitate compound/study team meetings.
+ Works Independently and collaborates with other functional areas.
#LI-Hybrid
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
**Uniquely Interesting Work, Life-changing Careers**
With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
**On-site Protocol**
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit careers.bms.com/ ( eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Bristol Myers Squibb is Disability Confident - Employer
A UK Government scheme
**Company:** Bristol-Myers Squibb
**Req Number:** R1594122
**Updated:** 2025-08-26 04:45:53.029 UTC
**Location:** Uxbridge-GB
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Clinical Specialist Cardiac Rhythm Management - Central UK, North West ideal
Posted 6 days ago
Job Viewed
Job Description
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 we are open to applications from passionate graduates 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
Clinical Specialist Cardiac Rhythm Management - Central UK (towards South Wales ideal)
Posted 6 days ago
Job Viewed
Job Description
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.
+ Prior experience within pacing/CRM and familiarity with cath lab procedures and protocol.
+ 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
Clinical Specialist Cardiac Rhythm Management - Central UK (ideal location towards Kettering/Camb...
Posted 6 days ago
Job Viewed
Job Description
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
Global Clinical Project Manager - Vendor Management Expert - Novartis Dedicated (home-based in Eu...
Posted 4 days ago
Job Viewed
Job Description
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
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Global Clinical Project Manager - Vendor Management Expert - Novartis Dedicated (home-based in Eu...
Posted 4 days ago
Job Viewed
Job Description
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
Clinical Operations Lead
Posted 2 days ago
Job Viewed
Job Description
Contract Clinical Operations Lead
Summary:
Join our client, a leading organisation in the pharmaceutical industry, as a Contract Clinical Operations Lead in! This is an exciting opportunity for a passionate professional looking to make a difference in clinical trial delivery. Enjoy a competitive daily rate ranging from 400 to 500, with a contract length of 12 months. Embrace a fulfilling full-time role in a vibrant and collaborative environment.
Key Responsibilities:
Ensure timely and efficient delivery of all operational aspects of one or more studies through all phases: start-up, conduct, and close down.
Represent the UK on the global study team, playing a pivotal role in driving study time lines and budgets.
Cultivate strong site relationships and oversee recruitment within the country of origin.
Provide direction and leadership to the local study team, including Clinical Research Associates (CRAs).
Collaborate with local Medical Affairs colleagues.
Engage with relevant country PDG colleagues to ensure timely feasibility, start-up, and site payments.
Drive the delivery of studies while ensuring compliance with quality standards, including ICH/GCP and applicable regulations.
Partner with PDG colleagues to respond to IRB, Health Authorities, and Ethics Committees, ensuring best practises are maintained throughout the study.
Who You Are:
You are a dynamic individual motivated by the mission to innovate clinical trial delivery. Your qualities include:
Customer-Centricity: You prioritise patient and site needs, fostering a culture of helpfulness and growth.
Growth Mindset: You embrace new experiences, encouraging learning and innovation.
Leadership Skills: You embody qualities of a Visionary, Architect, Catalyst, and Coach, inspiring and guiding diverse teams.
Problem-Solving Expertise: You are skilled in organising and planning, ensuring smooth clinical operations.
Effective Communicator: You listen attentively, ensuring transparent and strategic communication.
Join us in revolutionising clinical trial delivery and enhancing patient experiences! If you are ready to take on this impactful role, we encourage you to apply and bring your expertise to our client's ambitious vision. We can't wait to hear from you!
Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
Clinical Operations Manager
Posted 2 days ago
Job Viewed
Job Description
Clinical Operations Manager - 30 hours/week
Location: Hybrid - 1 day/week at Discovery Park in Sandwich on Wednesdays, rest remote
Hours: 30 hours/week (with flexibility and future potential to increase)
Salary: 32,000/annum (40,000/annum FTE)
- Holiday entitlement 25 days plus 1 day extra for each year of service up to 5 days extra.
- Pension Auto enrolment scheme with 3% contribution from the company
- Employee Assistance Programme (EAP), provided by Bupa for mental health and wellbeing advice and support for employees and their families.
CV's to (url removed)
Join the Future of Outpatient Care with eXroid UK
We're partnering exclusively with eXroid , a pioneering provider of non-invasive haemorrhoid treatment, to find an experienced Clinical Operations Manager who's ready to drive the future of outpatient care.
This is a unique opportunity to lead and evolve national clinical operations in a high-growth, patient-focused private healthcare setting.
As Clinical Operations Manager , you will be central to delivering eXroid's operational success - leading the delivery and expansion of clinic services across the UK. You'll take ownership of capacity planning, scheduling, performance management, and service quality while supporting business growth and clinical innovation.
You'll be responsible for:
- Leading the strategic planning and execution of UK clinic operations.
- Optimising doctor and clinic scheduling to maximise capacity, efficiency, and profitability.
- Managing the clinical booking system , stock and consumables, and clinic readiness.
- Onboarding and performance management of contracted doctors, clinics, and chaperones.
- Ensuring regulatory compliance (CQC, PMI) and leading QMS policy implementation.
- Driving service mobilisation and rollout for new service additions like homecare.
- Leading business continuity planning and supporting incident resolution and complaint handling.
What You'll Bring:
- Strong leadership and organisational skills within a fast-paced clinical or operational setting.
- Proven ability to manage clinic scheduling, capacity targets, and operational KPIs.
- Comfortable handling large volumes of data and managing reporting for the executive team.
- High emotional intelligence - empathy, patience, and confidence when speaking with patients.
- A hands-on, problem-solving mindset focused on continuous improvement and service quality.
- Experience in health services or clinical operations (desirable but not essential).
- Willingness to travel occasionally for clinic reviews across the UK.
Why Join eXroid?
- Innovative and patient-led : Be part of a business redefining outpatient care.
- Flexible, hybrid role : Shape your working hours with just one office-based day per week.
- Room to grow : Expand your hours and impact as the service continues to scale.
- Visible role : Direct influence on strategic decisions and service innovation.
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