Regulatory project manager Work, Jobs in Reading, Eng (with Salaries)

Associate Director, Regulatory Project Manager
CSL Behring —Maidenhead
- £170,000 - £210,000 a year
- Full-time
- Doctoral degree
- PMP
- Master's degree
13h
Global Regulatory Project Manager
Corteva Agriscience —Abingdon
- Bachelor's degree
- Business
- Communication skills
7d
Project Engineer
Pharmagraph —Wokingham
- £43,045.14 - £48,784.96 a year
- Full-time
- Microsoft Word
- AutoCAD
- Microsoft Excel
- Annual leave
- Employee assistance programme
Quick apply
PMO Coordinator
SSE —Reading
- £57,150 - £68,295 a year
- Microsoft Excel
- Organisational skills
- IT
- Employee discount
- Gym membership
4d
Project Manager
Wokingham Borough Council —Wokingham
- £46,142 - £51,357 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
- Employee assistance programme
Project Manager
Venta Global —Hook
- Full-time
- Employee discount
Quick apply
Compliance Manager
Reading Blue Coat School —Reading
- £50,000 a year
- Part-time
- Project management
- Bachelor's degree
- IT
- Free parking
- Employee assistance programme
Quick apply
4d
Senior Regulatory CMC strategy manager
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Employee assistance programme
13d
Quality Improvement and Regulation Manager
Barchester Healthcare —Guildford
- £45,000 a year
- Analysis skills
- Travel
- Mentoring
Quick apply
12d
Regional HSEQ Compliance Auditor
Network Plus —Reading
- £45,000 - £55,000 a year
- Nights as needed
- Project management
Quick apply
Programme Manager
University of Oxford —Oxford
- £49,119 - £53,483 a year
- Project management
- Leadership
Project Manager
Theolytics —Oxford
- Organisational skills
- IT
- Communication skills
- Flexible schedule
Medical Innovation Manager
Procter & Gamble —Reading
- £45,000 a year
- Full-time
- Doctoral degree
- English
- Employee stock ownership plan
Senior Project Manager - Infectious Diseases / Tuberculosis / Epidemiology
University of Oxford —Oxford
- £49,119 - £58,265 a year
- Analysis skills
- Project management
- University
- Annual leave
- Employee discount
13d
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Account Manager
Equans —Oxford
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Annual leave
- Employee assistance programme
Operations Delivery Manager
Unitspark Ltd —Theale
- £80,000 a year
- Full-time
- Management
- Supervising experience
- Project management
- Paid training
Quick apply
Quality and Risk Manager
Circle Health Group —Windsor
- Full-time
- Hospital
- Data analysis skills
- In-person
- Employee discount
- Life insurance
Quick apply
Programme Manager
Jet Engineering System Solutions Ltd —Farnborough
- £55,000 - £70,000 a year
- Part-time
- PMP
- English
- Business development
- Free parking
- Health & wellbeing programme
Quick apply
1d
Senior Programme Manager
AALTO —Farnborough
- Full-time
- PMP
- Microsoft Office
- Analysis skills
- Flexible schedule
Quick apply
5h

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Associate Director, Regulatory Project Manager

CSL Behring -
Maidenhead

Apply Now

Job details

Full-time
£170,000 - £210,000 a year
13 hours ago

Qualifications

Doctoral degree
PMP
Master's degree
Bachelor's degree
Business

Full job description

Entity: CSL Behring

Job Category: Research Development & Sciences

Job Family: R&D Project Management

Job Type: Full Time

Location: Maidenhead, England, United Kingdom

Employer Reference: R-282451

Job Description

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.

Could you be our next Associate Director, Regulatory Project Manager? The job is in our Waltham MA, King of Prussia PA, Glattbrugg Switzerland or Maidenhead UK Office. This is a hybrid position and is onsite three days a week.

You will lead global regulatory project planning and execution across CSL’s product portfolio, ensuring timely delivery of submissions and improvement initiatives aligned with GRA strategy. This role oversees submission coordination, and cross-functional collaboration to meet global health authority requirements and drive operational excellence.

Main Responsibilities & Accountabilities:

Regulatory Project Leadership

Lead end-to-end project management of regulatory initiatives and improvement projects (initiation through closure) within budget, scope, and timelines.
Develop, execute, and monitor project plans, risk logs, communication strategies, and status reporting.

Submission Coordination

Oversee regulatory submissions per CSL’s Global Submission Management Process.
Lead submission team meetings, content planning, tracking in RIMS, and ensure on-time, compliant submissions.
Liaise with global, regional, and local teams for successful execution

Continuous Improvement & Governance

Manage improvement projects portfolio in alignment with GRA strategy and executive priorities.
Support quarterly reporting to Portfolio Committee and implement process efficiencies.
Contribute to governance, best practices, and standardization across regulatory operations.

Management & Collaboration

May be required to manage Regulatory Project Managers
Leads cross-functionally with Regulatory, Clinical, Manufacturing, POE (GPM) and external partners.
Mentor junior project managers and support training on submission processes and tools.
Liaise with Regulatory Policy to ensure awareness and incorporation of policy changes into Regulatory strategy, planning, and execution

Qualifications & Experience

Bachelor’s degree in Life Sciences or Business required; advanced degree (MSc, PhD, MBA) and PMP certification preferred.
7+ years of experience in pharma/biotech industry with a focus on biologics and regulatory affairs.
7+ years’ experience managing global, cross-functional projects in a matrix environment.
Strong knowledge of global regulatory submission processes, drug development lifecycle, and project governance.
Demonstrated success in delivering complex projects on time and within scope.

The expected base salary range for this position at hiring is $170,000-210,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the time of this posting in MA. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.

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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.

Apply Now

Refine Your Search

regulatory project manager jobs in reading, eng

Associate Director, Regulatory Project Manager

Global Regulatory Project Manager

Project Engineer

PMO Coordinator

Project Manager

Project Manager

Compliance Manager

Senior Regulatory CMC strategy manager

Quality Improvement and Regulation Manager

Regional HSEQ Compliance Auditor

Programme Manager

Project Manager

Medical Innovation Manager

Senior Project Manager - Infectious Diseases / Tuberculosis / Epidemiology

Sr. Clinical Project Manager (Europe)

Account Manager

Operations Delivery Manager

Quality and Risk Manager

Programme Manager

Senior Programme Manager

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Our Benefits

You Belong at CSL

Equal Opportunity Employer

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