Associate director Work, Jobs in Wotton Underwood, Bkm (with Salaries)

Associate Director, Regulatory Project Manager
CSL Behring —Maidenhead
- £170,000 - £210,000 a year
- Full-time
- Doctoral degree
- PMP
- Master's degree
5d
Associate Director
AtkinsRéalis —Oxford
- Full-time
- Hybrid work
- Business development
- Leadership
Director, Portfolio Development Process & Standards Lead
CSL Behring —Maidenhead
- £230,000 - £270,000 a year
- Full-time
- Hybrid work
- Nursing
- Master's degree
- Bachelor's degree
Stock Associate
Coach —Bicester
- £30,160 - £32,000 a year
- Part-time
- Sales
- Customer service
- English
- Employee discount
Associate Director - Sports & Major Events
Steer —Hemel Hempstead
- Full-time
- Hybrid work
- Analysis skills
- Project management
- Travel
- Annual leave
- Employee assistance programme
Quick apply
Senior Campaign Manager
University of Oxford —Oxford
- £49,119 - £58,265 a year
- Full-time
- Hybrid work
- Project management
- School
- Marketing
13d
Evaluation Specialist: Associate / Associate Director
Steer —Hemel Hempstead
- Full-time
- Hybrid work
- Management
- No degree
- Contracts
- Annual leave
- Employee assistance programme
Quick apply
Associate Director
Dalcour Maclaren —Bicester
- Military
- Negotiation
- Free parking
- Annual leave
Quick apply
Sustainability Consultant (ESG Strategies and ISO Certifications)
Enovation Consulting Ltd —Silverstone
- Up to £45,000 a year
- Full-time
- Hybrid work
- English
- Microsoft Office
- Project management
- Free parking
Quick apply
Associate Director, Facilities and Engineering
Replimune —Abingdon
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Quick apply
10d
Associate Director/Director Business Development
Genomics —Oxford
- Full-time
- Hybrid work
- Business
- Annual leave
Medical Information Content Manager
Kyowa Kirin International —Marlow
- £57,558 - £115,988 a year
- Full-time
- Doctoral degree
Quick apply
Office Administrator - Aylesbury
Xeinadin —Aylesbury
- Microsoft Office
- Accounting
- Organisational skills
- Annual leave
- Employee assistance programme
Executive MBA Programme Manager
University of Oxford —Oxford
- £35,681 - £41,636 a year
- Full-time
- Hybrid work
- Customer service
- University
- Business
Associate Director, Internal Communications and Engagement
CSL Seqirus —Maidenhead
- Full-time
- Bachelor's degree
- Travel
- Leadership
Associate Case Manager
Active Care Group —Oxford
- £50 - £60 an hour
- Case management
- Travel
- Organisational skills
Quick apply
Associate Director, Product Marketing (Europe)
Immunocore —Oxford
- English
- Analysis skills
- Bachelor's degree
Head of Fundraising Development
Willen Hospice —Milton Keynes
- £43,042 - £49,681 a year
- Part-time
- Hospice
- Free parking
- Employee assistance programme
Associate Director- Transport Development Planning
Steer —Hemel Hempstead
- Full-time
- Hybrid work
- Business development
- Mentoring
- Annual leave
- Employee assistance programme
Quick apply
Programme Coordinator
Saïd Business School —Oxford
- £32,108 - £37,338 a year
- Full-time
- Hybrid work
- Organisational skills
- Communication skills
- School
2d

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associate director jobs near wotton underwood, bkm

Associate Director, Regulatory Project Manager

CSL Behring -
Maidenhead

Apply Now

Job details

Full-time
£170,000 - £210,000 a year
5 days 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

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Associate Director, Regulatory Project Manager