Clinical study manager Work, Jobs in Sidcup, Gtl (with Salaries)

Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership
IQVIA —London
- Full-time
- Remote
- Bachelor's degree
- Team management
- Leadership
- Work from home
9d
Clinical Services Manager
Signature Senior Lifestyle —Hendon
- £62,000 - £66,000 a year
- Nursing home
- Computer literacy
- Travel
- Free parking
- Annual leave
9d
Senior Clinical Research Manager
University College London —London
- £68,284 - £76,244 a year
- Full-time
- Master's degree
- Leadership
- Annual leave
- Employee assistance programme
12d
Clinical Trial Manager
Precision for Medicine —London
- Remote
- English
- Bachelor's degree
- Computer skills
Quick apply
Clinical Trial Monitor
University College London —London
- £43,981 - £52,586 a year
- Full-time
- Spanish
- No degree
- Travel
- Annual leave
- Employee assistance programme
11d
Clinical Data Strategy, Manager
Novartis —London
- £49,140 - £91,260 a year
- Full-time
- Hybrid work
Clinical Trial Manager
Precision Medicine Group —London
- Remote
- English
- Bachelor's degree
- Computer skills
Clinical Site Manager
Qureight Ltd —London
- Full-time
- Hybrid work
- Continuous improvement
- Organisational skills
- Time management
- Annual leave
- Life insurance
Quick apply
Clinical Data Manager II/Senior Clinical Data Manager
Precision for Medicine —London
- Remote
- Microsoft Word
- English
- Bachelor's degree
Quick apply
Education Coordinator (Taught Programmes)
University College London —London
- £43,981 - £52,586 a year
- Full-time
- Hybrid work
- Management
- University
- IT
- Annual leave
- Employee assistance programme
3d
Clinical Data Manager II/Senior Clinical Data Manager
Precision Medicine Group —London
- Remote
- Microsoft Word
- English
- Bachelor's degree
Clinical Quality Manager
TFS HealthScience —London
- Bachelor's degree
- Quality control
Quick apply
eClinical Coordinator (London)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Software troubleshooting
- English
- Annual leave
- Work from home
Fertility Advisor: Nurse/Midwife, Bank Position
Hertility —London
- From £30 an hour
- Monday to Friday
- Remote
- Nursing
- Paid training
EU Regulatory Affairs Manager
Amgen —London
- £48,957 - £66,237 a year
- Remote
- Conflict management
- AI
- Negotiation
- Work from home
Research Regulatory Facilitator
Imperial College London —White City
- £48,246 - £58,318 a year
- Full-time
- University
- Time management
- Annual leave
8d
eClinical Coordinator (London, Entry Level)
Medpace, Inc. —London
- Full-time
- Microsoft Word
- Software troubleshooting
- English
- Annual leave
- Work from home
Clinical Deputy Manager
Hallmark Care Homes —Hutton
- Full-time
- Computer literacy
- Computer skills
- Leadership
- Employee discount
- Referral programme
8d
Associate Director, Clinical Operations
TFS HealthScience —London
- Hybrid work
- Bachelor's degree
- Team management
- No degree
Quick apply
Healthcare KOL & Influencer Manager
Foundation Partners —London
- Business development
- Recruiting
- AI
Quick apply

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Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership

IQVIA -
London

Apply Now

Job details

Full-time
9 days ago

Benefits

Work from home

Qualifications

Healthcare research operations
Clinical research
Stakeholder collaboration
Bachelor's degree
Team management
Partnership building
Risk management
Multidisciplinary collaboration
Good Clinical Practice (GCP)
Project leadership
Leadership
Project management experience
Good Clinical Practice (ICH-GCP) guidelines

Full job description

London, United Kingdom | Full time | Home-based | R1560940

At IQVIA, our Senior Project Managers play a pivotal role in bringing innovative medicines to patients worldwide. You'll provide strategic leadership for complex global clinical trials, partnering directly with sponsors and cross-functional teams to deliver studies that accelerate the development of life-changing therapies.

This is an opportunity to lead large-scale, multi-regional studies focused on renal, obesity and/or MASH (Metabolic Dysfunction-Associated Steatohepatitis) for some of the world's most innovative pharmaceutical and biotechnology companies while expanding your leadership impact and helping shape the future of clinical research.

Why Join Global Study Leadership?

Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and customer-dedicated delivery models. You'll work on some of the industry's most complex global clinical trials, partnering directly with leading pharmaceutical and biotechnology sponsors across therapeutic areas including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Renal, Obesity, MASH (Metabolic Dysfunction-Associated Steatohepatitis), Cell & Gene Therapy, Infectious Disease, Ophthalmology and Women's Health. Supported by a collaborative global network, flexible ways of working and AI-enabled technology and data-driven insights, you'll have exceptional opportunities to broaden your expertise, expand your leadership impact and accelerate your career within one of the world's leading clinical research organizations.

What You'll Be Doing

As the strategic leader of your studies, you'll be accountable for the successful delivery of complex global clinical trials from start-up through close-out, ensuring quality, timeline, budget, regulatory and customer objectives are achieved.

Key Responsibilities

Lead the delivery of complex global and multi-regional clinical studies, driving operational excellence and successful study outcomes
Serve as the primary strategic partner for sponsors, providing leadership, guidance and innovative solutions to drive successful study outcomes
Provide leadership and direction to cross-functional teams across regions, fostering collaboration, accountability and high performance
Oversee study timelines, budgets, quality, risks, financial performance and operational delivery to ensure study success
Drive proactive risk management, issue resolution, decision-making and stakeholder alignment throughout the study lifecycle
Ensure studies are delivered in compliance with ICH-GCP, regulatory requirements and contractual commitments

What We're Looking For

Bachelor's degree in Life Sciences, Healthcare or a related scientific discipline
7+ years of clinical research experience, including significant project management experience leading global or multi-regional clinical trials within a CRO, pharmaceutical or biotechnology environment
Experience leading renal, obesity and/or MASH (Metabolic Dysfunction-Associated Steatohepatitis) global clinical studies is strongly preferred
Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements
Proven success leading cross-functional teams and managing study delivery, including timelines, budgets, quality, risks and operational performance
Demonstrated ability to build trusted sponsor relationships and effectively manage senior stakeholders in a global environment
Exceptional leadership, communication, problem-solving and decision-making skills
Passion for advancing clinical research and improving patient outcomes

Build Your Future with IQVIA

If you're looking for a role that combines global exposure, strategic leadership, sponsor partnership and meaningful work, we'd love to hear from you. At IQVIA, you'll have the opportunity to work on high-profile global studies, collaborate with industry-leading sponsors, leverage cutting-edge technology and build a rewarding career with one of the world's leading clinical research organizations, all while helping bring innovative treatments to patients faster.

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 https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

clinical study manager jobs in sidcup, gtl

Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership

Clinical Services Manager

Senior Clinical Research Manager

Clinical Trial Manager

Clinical Trial Monitor

Clinical Data Strategy, Manager

Clinical Trial Manager

Clinical Site Manager

Clinical Data Manager II/Senior Clinical Data Manager

Education Coordinator (Taught Programmes)

Clinical Data Manager II/Senior Clinical Data Manager

Clinical Quality Manager

eClinical Coordinator (London)

Fertility Advisor: Nurse/Midwife, Bank Position

EU Regulatory Affairs Manager

Research Regulatory Facilitator

eClinical Coordinator (London, Entry Level)

Clinical Deputy Manager

Associate Director, Clinical Operations

Healthcare KOL & Influencer Manager

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