Director, Clinical Paediatric and Rare Oncology

Director, Clinical Paediatric and Rare Oncology

Full-Time 80000 - 100000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead clinical strategy in paediatric and rare oncology, driving impactful programmes.
  • Company: LifeArc, a not-for-profit life science organisation focused on rare diseases.
  • Benefits: Flexible benefits, 31 days annual leave, private health insurance, and up to 12% pension contributions.
  • Other info: Join a diverse team committed to equity and inclusion in healthcare.
  • Why this job: Make a real difference in patients' lives while working in an inclusive and innovative environment.
  • Qualifications: Extensive clinical development experience in oncology and strong leadership skills required.

The predicted salary is between 80000 - 100000 £ per year.

Location: London

Job Type: Permanent with a hybrid working environment

Are you passionate about making life science life changing and delivering impact for patients? We want to hear from you.

About the role: The Director, Clinical Paediatric and Rare Oncology is a senior clinical leader responsible for shaping and delivering LifeArc’s clinical strategy in paediatric and adult rare oncology, aligned to LifeArc’s organisational mission and priorities. This role holds accountability for defining the clinical development strategy and driving the timely and quality execution of a portfolio of collaborative, and funded programmes. The Director works closely with senior leadership to ensure alignment and integration across the portfolio, maintaining high scientific and clinical rigour, clear decision‑making, and on time delivery of key milestones to progress assets through clinical development. Operating within a dynamic, matrixed environment, the Director provides strategic and clinical leadership of the rare oncology portfolio, ensuring alignment with the broader LifeArc clinical strategy. The role includes line management of a small team with responsibility for building and leading a high‑performing team and delivering portfolio outcomes in line with LifeArc’s strategic goals.

About you: Key responsibilities include:

  • Developing and implementing the clinical strategy in collaboration with LifeArc Pillars.
  • Chairing the clinical development team for rare oncology.
  • Responsibility for the delivery of clinical programmes to cost, quality and time.
  • Providing input on and may attend key clinical programme interactions e.g. regulatory authorities, HTAs to support successful delivery of clinical programmes.
  • Providing the review of key clinical project documentation.
  • Appraising and giving final recommendation on the pursuit of opportunities (including considerations on viability and developability) for clinical collaborations in rare oncology to CRM.
  • Responsibility for overseeing a budget and escalating planned variances or RFCs out of a pre‑defined tolerance window.
  • Responsibility for the effective reporting and communication of clinical programme progress towards corporate goals/clinical pillar objectives to Snr Leadership, Exec and external partners.
  • Sponsorship of new business cases in Clinical Pillar.
  • Leading and developing teams, including direct line management and cross‑functional teams to deliver results.
  • Responsibility for major decisions on clinical programmes, including risk management and resolution of complex challenges.
  • Responsibility for ensuring the development of frameworks, governance and SOPs/working practices for clinical pillar projects and programmes.
  • Potentially serving as the programme lead for programmes or projects.
  • Representing the organisation in high‑level forums and external partnerships/collaborations.
  • Being an ambassador and subject matter expert for the clinical pillar and LifeArc.

Essential experience required:

  • Extensive Global Clinical Development experience [Pharma/Biotech/Academia] in therapeutics, diagnostics, devices or other medical technologies.
  • Experience of developing and implementing clinical strategy.
  • Asset selection and/or programme prioritisation experience.
  • Clinical trial regulatory submission experience e.g. IND/CTA.
  • Product approval regulatory submission experience e.g. NDA/MAA/BLA.
  • National and International regulatory authority interactions.
  • Extensive therapeutic area expertise in oncology.
  • Demonstrate an in‑depth understanding of clinical research regulations.
  • Experience of building high performing and collaborative teams.
  • Demonstrable skills in line management.
  • Experience of paediatric oncology.
  • Experience of rare oncology.
  • Experience of paediatric drug development.

Education:

  • Minimum qualification of BSc Life Sciences [PhD or MD preferred].
  • Professional qualifications in clinical research, and clinical project management preferred.

Skills & abilities:

  • Skilled at building relationships and fostering cross‑functional teamwork in a matrix environment.
  • Self‑awareness and a high level of professionalism, a can‑do attitude and with a consistent track record of high impact delivery.
  • Can build and manage strategic collaborations.
  • Able to represent LifeArc as a credible clinical leader externally.
  • Ability to inspire direct reports and cross‑functional teams, influence stakeholders, and drive strategic initiatives.
  • Excellent communication and stakeholder management skills.
  • Able to manage clinical programme budgets and funding allocation.

About us: LifeArc is a not‑for‑profit life science organisation, leading the way for change in rare diseases in the UK and supporting promising initiatives in global health. We seek out research in areas of unmet need that has great potential, providing support to help it become breakthroughs that change lives.

What we can offer you: Focused on finding life changing solutions for underserved patients, our people thrive in an inclusive, and supportive environment that prioritises their health and wellbeing. Our multidisciplinary approach guarantees our people growth opportunities, while our culture of innovation and collaboration drives the impact we make delivering on our purpose of ‘putting patients at the centre of everything we do’.

LifeArc is committed to making our recruitment practices as inclusive as possible and developing a culture that values differences. As a Disability Confident Employer, we guarantee an interview to candidates with a disability or long‑term health condition who meet the essential criteria for the role.

Please note that in certain situations, such as high volumes of applications, it may not be practical to interview all eligible candidates. In these cases, we may need to select those best meeting the essential criteria.

Salary will be determined by qualifications and experience along with other exceptional benefits. Because we understand everyone has different requirements, our flexible benefits allow you to choose those which are important to you. Our pension scheme offers employer contributions of up to 12%, private health insurance, and annual leave of 31 days PLUS bank holidays.

Don’t meet every single requirement? Studies have shown that women and people from minority ethnic backgrounds, for example, are less likely to apply to jobs unless they meet every single qualification. At LifeArc we are dedicated to building a diverse, inclusive, and authentic workplace, so whatever your background or lived experience, if you’re excited about this role but your experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyway. Our top priority is finding the best candidate, and you may be just right for this or other roles.

At LifeArc, we commit to advancing equal opportunities and building a diverse workforce by ensuring a fair, inclusive, and accessible recruitment experience for all. We employ individuals based on their suitability for the work to be performed and their potential for development, regardless of age, sex, race, colour, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief. Our commitment to equity, diversity and inclusion includes creating a culture where everyone feels they belong, is valued for who they are and has the opportunity to translate their potential.

We want every candidate to do their very best. If you require special assistance or reasonable adjustments, please be sure to let us know in advance what will be most useful for you and/or to discuss your needs.

Please note we are actively recruiting, and the closing date may be brought forward if we find the right person for this role.

Director, Clinical Paediatric and Rare Oncology employer: LifeArc

LifeArc is an exceptional employer, dedicated to fostering a supportive and inclusive work environment in London, where employees are empowered to make a meaningful impact in the field of rare diseases. With a strong focus on employee wellbeing, professional growth, and collaboration, LifeArc offers competitive benefits including a generous pension scheme, private health insurance, and ample annual leave, ensuring that every team member can thrive both personally and professionally. Join us in our mission to transform lives through innovative solutions, while enjoying the unique advantages of working within a dynamic, not-for-profit organisation committed to advancing healthcare.

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Contact Details:

LifeArc Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Director, Clinical Paediatric and Rare Oncology

Tip Number 1

Network like a pro! Reach out to your connections in the life sciences field, especially those who have experience in paediatric and rare oncology. A friendly chat can lead to valuable insights or even job leads.

Tip Number 2

Prepare for interviews by brushing up on your clinical strategy knowledge. Be ready to discuss how you would shape and deliver a clinical strategy at LifeArc. Show us your passion for making a difference in patients' lives!

Tip Number 3

Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation and reiterate your enthusiasm for the role. It keeps you fresh in their minds.

Tip Number 4

Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in being part of our mission at LifeArc.

We think you need these skills to ace Director, Clinical Paediatric and Rare Oncology

Clinical Development Strategy
Oncology Expertise
Regulatory Submission Experience
Clinical Trial Management
Budget Management
Team Leadership
Cross-Functional Collaboration

Some tips for your application 🫡

Tailor Your Application:Make sure to customise your CV and cover letter to highlight your experience in clinical development, especially in paediatric and rare oncology. We want to see how your background aligns with our mission at LifeArc!

Showcase Your Leadership Skills:As a Director, you'll be leading teams and driving strategic initiatives. Use your application to demonstrate your leadership experience and how you've built high-performing teams in the past. We love to see examples of collaboration!

Be Clear and Concise:When writing your application, keep it clear and to the point. Highlight your key achievements and relevant experiences without fluff. We appreciate straightforward communication that gets to the heart of your qualifications.

Apply Through Our Website:Don't forget to submit your application through our website! This ensures we receive your details directly and can process your application efficiently. We can't wait to hear from you!

How to prepare for a job interview at LifeArc

Know Your Clinical Strategy

Before the interview, dive deep into LifeArc's clinical strategy, especially in paediatric and rare oncology. Be prepared to discuss how your experience aligns with their goals and how you can contribute to shaping their clinical development strategy.

Showcase Your Leadership Skills

As a Director, you'll need to demonstrate your ability to lead and inspire teams. Prepare examples of how you've built high-performing teams in the past, particularly in a matrixed environment, and be ready to discuss your approach to line management.

Understand Regulatory Interactions

Familiarise yourself with the regulatory landscape relevant to clinical trials and product approvals. Be ready to discuss your experience with regulatory submissions and interactions with authorities, as this will be crucial for the role.

Communicate Clearly and Confidently

Effective communication is key in this role. Practice articulating your thoughts clearly, especially when discussing complex clinical concepts. Be prepared to answer questions about your stakeholder management skills and how you ensure alignment across teams.