Clinical Trials jobs in Edinburgh
- IQVIALivingston
- 4 years of relevant experience in a clinical laboratory or clinical trials environment.
- IQVIA Laboratories helps sponsors enable laboratory testing in global…
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- IQVIALivingston
- 3 years of relevant experience in a clinical laboratory or clinical trials environment.
- Livingston, United Kingdom | Full time | Hybrid | R1568528.
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- IQVIALivingston
- Experience working on clinical trials.
- Experience in working with external data providers within a clinical study.
- Working knowledge of GCP/ICH guidelines.
- IQVIALivingston
- Experience working on clinical trials.
- Experience in working with external data providers within a clinical study.
- Working knowledge of GCP/ICH guidelines.
- ICON PlcLivingston
- Negotiate directly with assigned sites on all site related contracting items including clinical trial agreements, budgets, payment terms, ancillary agreements…
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- ICON PlcLivingston
- You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
- Life assurance and disability coverage.
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- Strong understanding of global clinical development, regulatory pathways, and therapeutic area dynamics.
- This role is designed for a seasoned commercial leader…
- IQVIALivingston
- 7 years of clinical or research industry experience, including 5 years project management experience preferred.
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- IQVIALivingston
- 4 years of relevant experience in a clinical laboratory or clinical trials environment.
- IQVIA Laboratories helps sponsors enable laboratory testing in global…
- View all IQVIA jobs - Livingston jobs - Associate Manager jobs in Livingston
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- Experience supporting clinical trial regulatory submissions in the UK.
- Collect, review, and prepare site and regulatory documentation required for UK clinical…
- Cencora, Inc.Edinburgh
- Most shifts fall between 08:00 and 18:00, though flexibility across the full window is required.
- As a Customer Service Consultant, you'll be the primary point…
- ICON PlcLivingston
- You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
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- ICON PlcLivingston
- Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry.
- Manage clinical and third-party data reconciliation…
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- Real ChemistryEdinburgh
- Possesses a good understanding and appreciation of the clinical trials process (phases, data representation, drug approval process and key statistical variables…
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- CatalentBathgate EH48 2FY
- We offer packaging design services on site, as well as secondary packaging and clinical labeling services.
- This role involves managing documentation, materials,…
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- CatalentBathgate EH48 2FY
- Experience in MDM, supply chain, clinical trial materials, pharmaceutical operations, or a regulated environment.
- Previous leadership or supervisory experience.
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Associate Manager - Immunology
Job details
Job type
Full job description
Livingston, United Kingdom | Full time | Office-based | R1568553
Associate Manager
IQVIA Laboratories – Central Laboratory Service
We are a comprehensive global central laboratory services supporting clinical trials in countries around the world. Meeting the demands of today’s drug, device and diagnostics development environment requires a next generation service provider.
IQVIA Laboratories helps sponsors enable laboratory testing in global clinical trials by providing specimen collection kits, a courier network, a biorepository, plus project management and data management. With extensive scientific expertise and industry leading capabilities in lab services, biomarkers, companion diagnostics, esoteric testing, high quality data and analytics, as well as global logistics and biorepository & specimen management, IQVIA Laboratories helps biotech and pharmaceutical companies meet their development needs.
Join us on our exciting journey!
Job Overview:
Responsible for supervising a team of lab staff and ensuring effective operational delivery and for setting day to day operational activities for the team with a focus on daily delivery.
Under the mentorship of management, responsible for hiring, training, and performance management of staff.
Supervises the daily activities of assigned laboratory work group(s) through appropriate delegation, technical skills training, and work supervision. Meets regularly with staff and senior management to discuss and resolve workload and technical issues.
Responsible for ensuring activity in the team meets safety guidelines. Drives individual accountability for safety across the team. Identifies opportunities for improvements in safety.
Responsible for the review of laboratory metrics to identify initiatives as well as establish additional metrics such as cost savings that are associated with process improvement initiatives.
Ensures policies, practices and procedures are understood and followed by direct reports, customers and stakeholders.
Ensures timely and appropriate resolution of CAPA and quality incidents, quality and compliance metrics, root cause analysis and improvement.
Assists in establishment and revision of laboratory policies and procedures. Maintains appropriate control and quality assurance procedures. Ensures compliance with safety requirements.
Requirements:
- Bachelor’s degree in a Human Biology based science.
- 4 years of relevant experience in a clinical laboratory or clinical trials environment. (Immunology based)
- Experience in technical leadership and cross-functional collaboration
- Proficiency with LIMS and other laboratory data systems.
- Familiarity with CAPA processes and quality systems
- Ability to analyse and interpret complex data.
- Ability to effectively coordinate and execute multiple tasks or projects simultaneously.
- Ability to effectively write scientific and technical documents
- Understanding of LEAN 6 Sigma principles
Join IQVIA to see where your skills can take you
- Global exposure
- Variety of therapeutic areas
- Collaborative and supportive team environment
- Access to cutting-edge and innovative, in-house technology
- Excellent career development and progression opportunities
- Work-Life Balance, with a strong focus on a positive well-being.
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
Office-based
You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.
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.