Key Stage Leader of Science Job at Swale Academies Trust (Sittingbourne)

Programme Lead of Computer Science

Elementa is recruiting for a Programme Lead of Computer Science for this popular...

Location

United Kingdom , Weston-super-Mare

Salary:

32916.00 - 51048.00 GBP / Year

Elementa Support Services

Expiration Date

Until further notice

Requirements

Qualified Teacher Status (QTS) or Qualified Teacher Learning and Skills (QTLS)
Proven experience teaching Computer Science/Computing at secondary level
Demonstrable experience in a leadership or management role, or readiness to step into one
Strong subject knowledge in Computer Science, including programming and digital literacy
Excellent communication, organisational, and interpersonal skills
A commitment to raising standards and inspiring students

Job Responsibility

Lead and manage the Computer Science department, setting high standards for teaching and learning
Plan, prepare, and deliver high-quality Computer Science and Computing lessons across Key Stages
Monitor, evaluate, and improve student progress through effective assessment and intervention
Lead curriculum development and assessment planning within the department
Mentor, support, and develop colleagues to promote professional growth and best practice
Create a positive, inclusive, and engaging learning environment
Work collaboratively with senior leaders and departmental staff to drive continuous improvement
Keep up to date with developments in the Computer Science and Computing curriculum and implement innovative teaching approaches

What we offer

Weekly Pay
PAYE Contract offering full employment protections
Training & Support – access to free or discounted training, including Safeguarding, Behaviour, Team Teach, SEND, Makaton, and Thrive
Dedicated welfare support from a candidate manager
Fair Pay Policy – candidates are paid to scale

Fulltime

Business Developer France Cardiac Device Monitoring

We are looking for a high-performing Business Developer CIED professional to cap...

Location

France , Paris

Salary:

45000.00 - 55000.00 EUR / Year

Implicity

Expiration Date

Until further notice

Requirements

Proven experience (5+ years) in medical device sales, with a track record of exceeding quotas
Ideally focused on cardiovascular implants (Pacemakers, ICDs) or complex digital health solutions within the hospital setting
Direct experience working with electrophysiologists and cardiologists in France/Europe, and navigating public and private hospital procurement processes (Bonus)
Master’s Degree in Business, Biomedical Engineering, Life Sciences, or a related field
Strong hunter mentality with tenacity
Ability to quickly build trust with clinical key opinion leaders (KOLs)
Unwavering commitment to ethical sales practices and rigorous adherence to healthcare compliance standards (GDPR, HIPAA)
Highly autonomous, capable of managing a large territory, prioritizing activities, and maintaining clean data in the CRM (Salesforce)

Job Responsibility

Proactively identify, prospect, and acquire new hospital sites and cardiology practices using CIEDs to adopt the Implicity platform
Own and manage the full sales lifecycle, from initial outreach and qualification through clinical and technical presentations, negotiation, and contract closure
Utilize your knowledge of CIEDs and the cardiology ecosystem to articulate the clinical and economic value of our platform
Develop and execute a comprehensive territory sales plan focused on achieving aggressive quarterly and annual revenue targets (Quota)
Ensure smooth client handoffs to the Customer Success team post-sale and provide actionable market intelligence back to the Product team
Cultivate and maintain strong relationships with key decision-makers and influencers within target accounts
Provide accurate sales forecasts and actively monitor competitor activity to adjust sales strategies
Ensure meticulous use of Salesforce to document all sales activities, pipeline stages, and customer interactions

What we offer

Health care plan: Alan (50% employer)
Luncheon voucher: 9€ (50% employer)
Transport: 50% of your pass OR sustainable mobility pass
Employees stock option plan (BSPCE) subject to customary conditions
Regular team events, especially every Thursday evenings
Beautiful office at 29 rue du Louvre, 75002, PARIS

Fulltime

Head of Commercial Development

MedicQuant is a fast‑growing diagnostics startup developing a breakthrough platf...

Location

Denmark , Aarhus

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

5+ years of experience in diagnostics, medtech, or life science commercialization
Experience in market strategy, commercial development, or similar roles
Experience with reimbursement, market access, or health economics (directly or via consultants) is an advantage
Experience or networks in UK, Germany, or US markets is a plus
Comfortable operating in a hands‑on, execution‑focused environment typical of early‑stage companies
Strong analytical skills and the ability to translate insights into commercial strategy
Excellent communication and stakeholder management abilities
Bachelor’s degree required
advanced degree in business, life sciences, or related fields is a plus

Job Responsibility

Identify and assess new market opportunities through research and engagement with Key Opinion Leaders (evaluating unmet needs, market size, and competitive dynamics) to guide portfolio strategy
Build and maintain strong relationships with clinical Key Opinion Leaders
Identify corporate partners who can benefit from integrating the MedicQuant platform and develop compelling value propositions
Establish commercial partnerships with pharma companies where the technology can support clinical studies or complement their products
Drive reimbursement strategy across key geographies
Select and manage consultants for reimbursement, coding, and payer engagement
Support mapping of reimbursement pathways and creation of payer materials
Negotiate pricing levels with customers
Lead health economic and value demonstration work in collaboration with consultants to support value‑based pricing and reimbursement
Develop value dossiers, cost‑effectiveness models, and economic evidence that strengthens the value proposition together with consultants

What we offer

The opportunity to shape the commercial foundation of a breakthrough diagnostic platform from an early stage
A role with significant strategic influence, working closely with the leadership team to define market, pricing, and go‑to‑market directions
A dynamic, collaborative environment where your ideas directly impact product development, evidence strategy, and future launch success
Cross‑disciplinary exposure spanning scientific, clinical, and commercial domains
Flexibility, autonomy, and ownership of meaningful work in a fast‑moving, mission‑driven setting
Aarhus-based office with possibility for a hybrid working model combining remote and on‑site work

Fulltime

Vice President, Market Access, Commercial

Reporting to the Chief Commercial Officer, the Vice President, Market Access, Co...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

An advanced degree (Master's or Doctorate) in life sciences, business/finance, or a related field is preferred
15+ years of progressive experience in biopharma market access, pricing, health economics, or related areas, with a significant track record in senior leadership roles
Specific experience in cell and/or gene therapy, or launching other complex, rare disease therapies, is critical
Exceptional strategic thinking, commercial acumen, communication, negotiation, and leadership skills
A robust network within the biopharmaceutical industry, including relationships with key payers, hospitals and related thought leaders is vital
Strong team orientation and passion for continuous self-development

Job Responsibility

Develop and implement global and/or U.S. market access strategies that align with corporate goals and drive successful product launches
Cultivate relationships and lead negotiations with key stakeholders, including national and regional payers, government agencies (e.g., CMS), hospitals and policymakers, to secure and maintain optimal coverage and reimbursement
Lead the creation and communication of the product's value story, including clinical, economic, and health-related quality of life (HRQOL) value propositions, using evidence generation plans in partnership with Medical Affairs
Define and execute U.S. and global pricing strategies, balancing market competitiveness and access goals, while adhering to federal and state regulations
Partner with R&D, Commercial, Medical Affairs, Regulatory, Finance, and Supply Chain teams to ensure market access strategies are integrated into all stages of product development and commercialization
Proactively navigate evolving healthcare legislation and reimbursement models and optimize site-of-care strategies and provider logistics for the unique delivery of cell therapies (e.g., hospital-administered or specialty distribution models)
Establish and build a market access organization, overseeing a team of market access professionals and managing external advisors and consultants

What we offer

health and retirement, PTO, and stock option plans

Director, Clinical Pharmacology

We are seeking a motivated Director, Clinical Pharmacology, to join our growing ...

Location

United States

Salary:

230000.00 - 260000.00 USD / Year

Apogee Therapeutics

Expiration Date

Until further notice

Requirements

PhD or PharmD with relevant expertise in clinical pharmacology or pharmaceutical science
5+ years of direct industry experience in conducting clinical stage drug development
Experienced in developing clinical pharmacology plans and authoring relevant sections of clinical and regulatory documents
Knowledge and experience in the application of current practices in the areas of clinical pharmacology, pharmacokinetic and pharmacodynamic principles, drug metabolism, bioanalysis, biopharmaceutics
Fluency in model-informed drug development
Experience working with external CROs
Proficient in using common PK/PD modeling software (such as Phoenix WinNonlin, Prism, and other similar tools)
Ability to work proactively and effectively, with exceptional creative problem-solving skills and self-motivation
Ability to work in cross-functional teams within a highly dynamic environment
Strong project management skills with a high sense of urgency, ability to collaborate and influence effectively cross-functionally

Job Responsibility

Lead clinical pharmacology programs in immunology & inflammation, providing strategic planning for drug development activities
Influence, decide, and recommend key clinical pharmacology strategies across the drug development spectrum
Develop and help implement quantitative approaches to drug development programs
Work in close collaboration with different functions
Lead and present key Clinical Pharmacology information to teams, senior leaders, regulatory agencies, and external partners
Independently lead Clinical Pharmacology/PK/PD activities and provide scientific and strategic expertise
Support pediatric development, including protocol development and dose selection
Develop and oversee implementation of clinical pharmacology studies from protocol development to final study reporting
Lead the analysis, interpretation, and reporting of clinical PK/PD data, author clinical study reports
Develop and execute and/or oversee PK/PD modeling strategies to describe the relationship between drug exposure and response

What we offer

Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
Three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave
Commitment to growing you professionally and providing access to resources to further your development
Apogee offers regular all team, in-person meetings to build relationships and problem solve

Fulltime

Cardiovascular Therapeutic Area Lead

The TA Lead is the primary point of Medical accountability for assigned Therapeu...

Location

South Korea , Seoul

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctor of Medicine (MD) degree is highly preferred
Advanced degree (eg. PhD, PharmD, MPH) in relevant scientific areas is preferred, majoring in pharmacy or science/bio-based areas
≥ 5 years of medical affairs and/or clinical development experience in multinational pharmaceutical company(es)
≥ 2 years of direct people management experience
In-depth knowledge in clinical development, product lifecycle and commercialization process
Knowledge and deep understandings of local healthcare systems and pharmaceutical industry
Experience of assigned Therapeutic area is preferred
Knowledge of Good Clinical Practices (GCP), regulations and guidelines, and applicable international regulatory requirements
Proven ability to lead, manage, and motivate others in a complex, multi-functional, multi-national matrix environment
Prioritization, problem solving skills with strategic thinking, self-leadership/motivation

Job Responsibility

Develop and ensure the execution of patient-focused Therapeutic Area medical strategies that maximize the value proposition of Amgen's therapies including annual strategic planning and goal setting, launch support and lifecycle management, in collaboration with appropriate cross-functional teams and governance, ensuring alignment of early-stage strategy with late-stage TA objectives
Partner with cross functional stakeholders to shape the healthcare ecosystem by enabling access to medicines through evidence generation, scientific communication and education of medical value
Provide strategic input with high-impact insights and ensure operational excellence
Develop the strategy for scientific engagement across a broad range of stakeholders to strengthen understanding of the unmet needs and value of the product
Demonstrate medical leadership with external healthcare community, including scientific interactions with opinion leaders, payers, academic societies and industry associations for exchange
Lead evidence generation that reinforces our product position and informs the practice of medicine ensuring alignment of early-stage strategy with late-stage TA objectives
Contribute as a key member of the AUEG Governance Meeting
Foster Amgen‘s reputation as a science-based, innovative and patient-focused reliable partner
Manage medical therapeutic area budget and resources
Manage subordinates, eg. MSL(s), Med Advisor(s), to maximize their potential and perform their best. Recruit, retain, coach, mentor, motivate and develop talent.

Global Development Product Lead

Leads multiple cross functional oncology product teams from pre-clinical candida...

Location

United States , La Jolla; Cambridge; Bothell; South San Francisco; New York City

Salary:

295900.00 - 478800.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

MD or MD-PhD with 10+ years of industry experience in oncology drug development is preferred, track record in oncology clinical research including early phase drug development
Clinical oncology experience: Board certification in oncology preferred
Significant industry leadership experience in clinical, translational or basic research in biomedical sciences or one of the disciplines related to drug development
Understanding of related disciplines (e.g., biostatistics, regulatory, pre-clinical pharmacology, pharmaceutical sciences)
Demonstrated scientific productivity (publications, abstracts, etc.)
Proven scientific writing skills and good communication skills
Proven leadership skills with ability to defend the clinical plan at governance meetings is essential
Capacity to adapt to a fast-paced and changing environment
Demonstrated history of effective leadership
including cross functional and matrixed teams, managing direct reports when applicable, and experience in seeking and maintaining alignment with cross-functional leaders

Job Responsibility

Leads multiple (~2-4) cross functional oncology product teams from pre-clinical candidate nomination (CAN) through Phase 1-2 clinical development and proof of concept (POC) stages
In close collaboration with functional experts on the product teams, drives the effective integration of an end-to-end cross functional molecule strategy and risk mitigation plan and ensures delivery of data-driven milestones through successful risk identification and mitigation
Support clinical trials and the development strategy for early development assets and lead development programs across multiple functions within Pfizer Oncology, as well as represent the program with the external clinical community
Develop clinical development plan from first in human clinical trial to proof-of-concept, including assessment of appropriate combinations, as well as evaluation of potential predictive and pharmacodynamics biomarker plans
To ensure the cross-functional components of the product plans including clinical expertise are provided to project teams, including medical monitoring of clinical trials
Substantial support of CDP development and diligence for external innovation activities
Lead key enterprise level cross-functional workstreams to accelerate R&D decision making
Lead, develop and execute strategic development for early development assets
Ensure timely execution and delivery of product milestones within budget
Communicate with executive management and governance committees to address program needs and provide recommendations

What we offer

Participation in Pfizer’s Global Performance Plan with a bonus target of 30.0% of the base salary
Eligibility to participate in our share based long term incentive program
401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
Paid vacation, holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage
Relocation assistance may be available based on business needs and/or eligibility

Fulltime

Business Value Modeling Consultant

Robert Half Management Resources is looking for a Business Value Modeling Consul...

Location

United States , Salt Lake City

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Advanced expertise in Microsoft Excel, including building complex, auditable financial models from the ground up
Strong background in financial modeling, forecasting, valuation analysis, and business case development
Experience with revenue modeling, cost estimation, profitability analysis, and return metrics such as ROI
Understanding of market sizing approaches and the factors that influence commercial potential for new products
Ability to work effectively with stakeholders across scientific, commercial, strategic, and financial functions
Strong analytical and communication skills with the ability to explain complex model outputs clearly
Prior experience in life sciences, biotechnology, or pharmaceuticals is preferred, though exceptional modeling capability from another industry will also be considered

Job Responsibility

Build dynamic financial models that evaluate the long-term value and commercial potential of life sciences products and early-stage concepts
Assess market opportunities by estimating addressable demand, reachable segments, and realistic capture potential across therapeutic areas or product categories
Create revenue forecasts using key assumptions such as patient population trends, pricing strategy, adoption patterns, and competitive activity
Partner with cross-functional stakeholders to estimate development, clinical, manufacturing, and launch-related costs for product initiatives
Prepare valuation analyses such as net present value, internal rate of return, and related return metrics to support investment decisions
Develop scenario and sensitivity models to show how timeline shifts, market changes, or clinical outcomes may affect financial performance
Gather, validate, and synthesize inputs from technical, commercial, and finance teams to maintain model accuracy and transparency
Present findings and recommendations in a clear format that enables senior leaders to compare opportunities and risks effectively

What we offer

Medical, vision, dental, and life and disability insurance
401(k) plan
Free online training

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Key Stage Leader of Science

Swale Academies Trust

Location:
United Kingdom , Sittingbourne

Category:
Education

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
April 16, 2026

Expiration:
April 17, 2026

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Our AI answers in your language

Key Stage Leader of Science

Swale Academies Trust

Location:United Kingdom , Sittingbourne

Category:Education

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:April 16, 2026

Expiration:April 17, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Key Stage Leader of Science

Programme Lead of Computer Science

Business Developer France Cardiac Device Monitoring

Head of Commercial Development

Vice President, Market Access, Commercial

Director, Clinical Pharmacology

Cardiovascular Therapeutic Area Lead

Global Development Product Lead

Business Value Modeling Consultant

Location:
United Kingdom , Sittingbourne

Category:
Education

Contract Type:
Not provided

Job Posted:
April 16, 2026

Expiration:
April 17, 2026