Research manager Work, Jobs in Tadley, Ham (with Salaries)

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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
Laboratory Manager- 12 month fixed term contract
QinetiQ —Farnborough
- £43,200 - £48,000 a year
- Full-time
- Laboratory experience
- Continuous improvement
- Communication skills
- Employee discount
Network Director - NIHR South East Regional Research Delivery Network
Royal Surrey NHS Foundation Trust —Guildford
- £115,052 - £132,053 a year
- Full-time
Senior Director, Drug Development
IQVIA —Reading
- Full-time
- Remote
- Microsoft Powerpoint
- Master's degree
- Business development
- Work from home
Research Director
MMR Research —Wallingford
- Full-time
- Hybrid work
- Business development
- Mentoring
- Leadership
Quick apply
Project Manager - Aerospace/Space
TISICS —Farnborough
- Organisational skills
- Leadership
- Communication skills
Associate Director, R&D Project Management
CSL Behring —Maidenhead
- Full-time
- Engineering
- Bachelor's degree
- Mentoring
Laboratory Manager (Health, Medical and Psychology)
University of Surrey —Guildford
- £37,694 - £46,049 a year
- Full-time
- Hybrid work
- Management
- University
- Psychology
- Relocation assistance
Research Manager - (Food, drink and personal care)
Eurofins Sensory, Market Research and Product Design —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- English
Quick apply
Senior Clinical Trial Case Manager
CSL Behring —Maidenhead
- Full-time
- Doctoral degree
- Master's degree
- Bachelor's degree
Manager R&D Labs (CNAP)
Convatec —Abingdon
- Full-time
- Doctoral degree
- Engineering
- Recruiting
Business Development Director (Clinical Research), UK and Nordics
Ergomed —Guildford
- Full-time
- Remote
- Sales
- Business development
- Analysis skills
Quick apply
Lead Data Scientist
UK Atomic Energy Authority —Culham
- £71,815 a year
- Full-time
- Doctoral degree
- Research
- Machine learning
- Annual leave
- Employee assistance programme
Lead Pricing Scientist - Hybrid Working
Punter Southall Group —Reading
- Full-time
- Hybrid work
- AI
- Business
- Communication skills
7d
Communications & Networking Research – Software Solution lead
Thales —Reading
- Full-time
- Computer networking
- Leadership
- Annual leave
- Employee assistance programme

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Unum Group —Basingstoke
Acting as a trusted risk partner to operational teams, helping translate risk concepts into clear, practical actions for non-risk stakeholders.

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Director, Portfolio Development Process & Standards Lead

CSL Behring -
Maidenhead

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Job details

Full-time
£230,000 - £270,000 a year

Qualifications

Nursing
Clinical research
Stakeholder collaboration
Stakeholder liaison
Process improvement
Master's degree
Change management
Bachelor's degree
Change leadership
Good Clinical Practice (GCP)
Research & development
Project management experience
Good Clinical Practice (ICH-GCP) guidelines

Full job description

Entity: CSL Behring

Job Category: Research Development & Sciences

Job Family: Clinical Development Operations

Job Type: Full Time

Location: Maidenhead, England, United Kingdom

Employer Reference: R-281885

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 Director, Portfolio Development Process & Standards Lead? This position is located in our King of Prussia, PA Waltham MA or Maidenhead UK office. It is a hybrid role three days onsite. You will report to the Head, Porfolio Development Excellence, Process & Compliance.

You will be responsible for establishing and maintaining a framework that allows the Global Portfolio Development group, in collaboration with multiple partner functions across the organization, to plan, evaluate and report clinical trials and programs under highest quality standards

REQUIREMENTS:

Portfolio Development Excellence: Procedures, training, continued learning, and guidance

Manages all Portfolio Development (CD/BM/CO) owned SOP updates in collaboration with critical partner SMEs where appropriate and ensures they are updated to reflect current processes and structure
Drives the development of a fit for purpose technical training curriculum across PD that supports achieving quality program goals and standards.
Provides guidance on process/procedural expectations and stakeholder management.

Driving excellence through change management and objectives oversight in partnership with PD Chief of Staff

Tracks and manages all Portfolio Development sponsored process development / improvement initiatives, in collaboration with the appropriate delegates and surface to PD CoS Identifies and drives cross functional initiatives to bring in technology
May sponsor or lead cross-functional initiatives supporting design and execution excellence
Tracks and manages all procedural documents update requirements to ensure compliance across the department in collaboration with the Portfolio Development Leadership Team and appropriate delegates.
Provides innovative solutions to increase the excellence of Portfolio Development; aiming to reduce complexity, increase quality and speed, and reduce decision making churn.
Represents Portfolio Development for applicable cross-functional R&D initiatives and forums.
Core reviewer on all Portfolio Development SOP updates to ensure changes work systematically across procedural documents.

QUALIFICATIONS:

Bachelor’s degree or equivalent in life sciences, nursing, pharmacy, medical laboratory technology, or other health/medical related area preferred.
Other degrees and certifications considered if commensurate with related clinical research experience (e.g., diploma or associate degree RN, certified medical technologist).
12+ years experience in the biotechnology or pharmaceutical industry (or biomedical research organization)
In-depth knowledge of drug development and GCP environment
5+ years experience in managing projects in Clinical Research and Development, first-hand experience in the execution of clinical trials is required
3+ years experience in managing process improvement initiatives, and influencing change in an organization.
Proven experience in leading cross-functional, multicultural and international (product development) teams

The expected base salary range for this position at hiring is $230,000- $270,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the listed for Waltham MA at the time of this posting. 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.

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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research manager jobs in tadley, ham

Director, Portfolio Development Process & Standards Lead

Laboratory Manager- 12 month fixed term contract

Network Director - NIHR South East Regional Research Delivery Network

Senior Director, Drug Development

Research Director

Project Manager - Aerospace/Space

Associate Director, R&D Project Management

Laboratory Manager (Health, Medical and Psychology)

Research Manager - (Food, drink and personal care)

Senior Clinical Trial Case Manager

Manager R&D Labs (CNAP)

Business Development Director (Clinical Research), UK and Nordics

Lead Data Scientist

Lead Pricing Scientist - Hybrid Working

Communications & Networking Research – Software Solution lead

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Job Description

About CSL Behring

Our Benefits

You Belong at CSL

Equal Opportunity Employer

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