Clinical trial manager Work, Jobs in Hampton, Gtl (with Salaries)

Manager, Regulatory Clinical Trial Authorization (CTA)
CSL Behring —Maidenhead
- Full-time
- Customer service
- Computer literacy
- English
Clinical Trial Associate Manager
Galderma —London
- Hybrid work
- Project management
- Bachelor's degree
- Leadership
Clinical Trial Manager
Precision for Medicine —London
- Remote
- Microsoft Powerpoint
- Management
- English
Quick apply
1d
Clinical Trials Manager
Imperial College London —London
- £46,614 - £56,345 a year
- Full-time
9d
Trial Vendor Senior Manager - Global Clinical Operations
Novartis —London
- £49,140 - £91,260 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Communication skills
2d
Clinical Trial Manager
Precision Medicine Group —London
- Remote
- Microsoft Powerpoint
- Management
- English
1d
Clinical Trials Manager
Gilead Sciences —Uxbridge
- Full-time
- Hybrid work
- Travel
- Organisational skills
- Communication skills
GCP Compliance Manager - Clinical Programs & Trials
Novartis —London
- Full-time
- Hybrid work
- Engineering
- Communication skills
Manager, Clinical Study Lead
Regeneron —Uxbridge
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
3d
Project Management Team Lead – Clinical Trials (f/m/d)
Clariness GmbH —London
- Full-time
- English
- Project management
- Mentoring
- Flexible schedule
Quick apply
8d
Senior Clinical Trial Manager - Tooting (Redeployee Applicants Only)
City St George's, University of London —London
- University
- Leadership
8d
Radiology Research Manager (EF:100)
King's College Hospital NHS Foundation Trust —London
- £58,133 - £65,261 a year
- Full-time
2d
Project Manager, Clinical Trials
Cogstate —London
- £55,000 - £60,000 a year
- Remote
- Computer Science
- Engineering
- Master's degree
- Annual leave
Quick apply
Principal Clinical Research Specialist
Medtronic —Watford
- £64,800 - £97,200 a year
- Full-time
- Travel
- Organisational skills
- Communication skills
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)
サイネオス・ヘルス —London
- Bachelor's degree
- Contracts
- Communication skills
Study Manager, Clinical Operations
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Project management
Quick apply
Quality Manager - GCP (with GMP awareness)
Ellipses Pharma —London
- Project management
- Travel
- Communication skills
8d
Study Start Up Specialist
Novo Nordisk —Gatwick Airport
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
8d
Clinical Study Manager
Qureight Ltd —London
- Full-time
- Hybrid work
- Project management
- Machine learning
- Annual leave
- Life insurance
Quick apply
1d

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clinical trial manager jobs near hampton, gtl

Manager, Regulatory Clinical Trial Authorization (CTA)

CSL Behring -
Maidenhead

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Job details

Full-time

Qualifications

Customer service
Computer literacy
English
Master's degree
Bachelor's degree
Environmental issues
Communication skills

Full job description

Entity: CSL Behring

Job Category: Research Development & Sciences

Job Family: Global & Regional Regulatory Affairs

Job Type: Full Time

Location: Maidenhead, England, United Kingdom

Employer Reference: R-277348

Job Description

Overview:

The Manager, Clinical Trial Authorization (CTA) is responsible for ensuring that CTA activities for assigned clinical studies are planned, governed, and overseen in line with CSL regulatory expectations, quality standards, and development timelines.

Reporting to the Director, Global Regulatory CTA, the role translates global CTA direction into clear, study‑specific regulatory approaches, provides guidance to Study Teams and partners, and acts as the first line CTA point of contact across functions. The position ensures that CTA activities delivered by external partners are appropriately overseen, risks are identified early and managed proactively.

The role maintains a strong focus on quality, inspection readiness, and continuous improvement by monitoring performance, contributing to metrics and dashboards, driving pragmatic process enhancements, and representing CTA internally during audits and inspections, as required. This role reports to the Director, Global Regulator CTA

Responsibilities:

CTA Strategy Implementation & Regulatory CTA Support

Translate global CTA strategies into study‑level regulatory approaches, ensuring alignment with development priorities and applicable regulatory requirements delivered via outsourced partners.
Provide CTA guidance and strategic direction to external service providers, Study Teams, and cross‑functional stakeholders within the approved framework.
Support early risk‑based CTA planning for critical or complex studies, including country approach, sequencing considerations, and identification of regulatory sensitivities.
Ensure consistent application of regulatory intelligence and evolving requirements across assigned studies.
Act as the internal CSL CTA interface for assigned clinical studies, providing cross‑functional coordination and governance oversight within the outsourced delivery model.

Oversight of Outsourced CTA Activities

Act as the primary oversight contact for external partners performing CTA activities.
Execute defined risk‑based oversight activities in line with established governance, oversight plans and ways of working documents.
Monitor vendor performance against agreed KPIs, timelines, and quality expectations and contribute to joint improvement initiatives with partners.

Quality, Compliance & Inspection Readiness

Ensure outsourced CTA activities are conducted in compliance with GCP requirements and internal procedures.
Support preparation for Health Authority inspections, audits, including participation as the internal reg CTA representative.
Proactively escalate compliance risks or deviations and propose appropriate mitigation actions.

Process Adherence & Continuous Improvement

Proactively ensure adherence to CTA processes and working practices supporting the outsourced delivery model.
Continuously identify process inefficiencies, quality issues, or recurring risks impacting CTA delivery or oversight and drive improvement actions.
Lead and support implementation of approved process changes, tools, and templates in collaboration with relevant stakeholders.
Actively contribute to CTA metrics, dashboards, and reporting to strengthen oversight and inform decision‑making.

Qualifications:

Education:

A degree (BSc/MSc) or equivalent in life science, pharmacy or other health/medical related field

Experience:

A minimum of 5 years’ experience in managing Clinical Trial Authorizations
Strong experience with CTA requirements and processes, including EU CTR.
Experience working with or overseeing external vendors/CROs.
Extensive and comprehensive knowledge of ICH guidelines/GCP and current medical/scientific/regulatory knowledge incl. inspection expectation

Competencies

Demonstrated ability to problem solve and use clear judgment in relation to regulatory requirements, interactions with external parties, timelines, and complex clinical studies
Strong regulatory judgment within defined strategic frameworks
Structured, risk‑based oversight mindset
Ability to manage complexity and priorities in a matrix environment
Clear communication and issue escalation skills
Quality‑ and compliance‑focused approach
Customer service focus
Excellent written and oral communication skills in English
Maintains computer literacy in appropriate software

About CSL Behring

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.

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