At a Glance
- Tasks: Support clinical data generation and reporting in oncology drug development.
- Company: Ellipses, a global leader in oncology drug development with a collaborative culture.
- Benefits: Flexible working options, competitive salary, and opportunities for professional growth.
- Other info: Embrace a hybrid work environment that values collaboration and innovation.
- Why this job: Join a dynamic team making a real impact in cancer research and drug development.
- Qualifications: 10+ years in early-phase oncology development and a degree in Life Sciences or related field.
The predicted salary is between 60000 - 80000 £ per year.
Ellipses is a global clinical-stage drug development company focused on progressing first- or best-in-class oncology drugs. Ellipses’ maturing clinical pipeline is progressing three clinical phase-2 programmes with an additional programme due to commence Phase 1 studies in 2026. Ellipses is supported by a global Scientific Advisory Group comprising over 300 leading Oncology Key Opinion Leaders to de-risk initial asset selection and provide critical insights into clinical trial design.
An Interim Senior Clinical Scientist is sought to provide temporary support in the Sponsor oversight of clinical data generation and reporting. Candidates will be a self-starter, able to drive collaboration across internal cross-functional teams and external service providers to ensure processes, plans and core study documents are robust and consistent, enabling communication of reliable data in accordance with development strategy.
Key Responsibilities:- In collaboration with Clinical Operations, define processes for oversight of clinical data generation, and maintain a clinical data delivery plan that defines the timing and specification of outputs to serve strategic decision making, scientific publication and business development deliverables.
- Act as a Subject Matter Expert for clinical study protocol development, contributing to design elements, enabling delivery of key endpoints/Critical to Quality factors, conducting literature reviews and participating in discussions with key opinion leaders and other contributors as appropriate.
- Support the development of other key regulatory and operational documents including e.g. Statistical Analysis Plans, Investigators Brochures, Development Safety Update Reports, briefing documents.
- Execute key components of the medical communications plan, e.g. manuscripts, working cross-functionally to coordinate authoring, review and approval.
- A degree in a Life Sciences, Pharmacy or health-related field.
- A minimum of 10 years’ experience in an early-phase oncology clinical development role within biotech, pharma or CRO is essential.
- Solid understanding of clinical research methodologies, regulatory guidelines, and Good Clinical Practice.
- Familiarity with biostatistics and data analysis.
- Self-starter, able to work in an agile, hands-on environment.
- Collaborative and a strong communicator.
- Solution focused.
Ellipses Pharma is an organisation that values the strength of collaboration, inclusive and quick decision making, knowledge sharing and a culture built on working together on site. As a small but growing company face to face interaction is highly valued. We recognise that a more hybrid approach is at times required and we do support some element of remote working where operationally appropriate to help employees with work life integration. By balancing in-person presence with occasional remote working, we ensure we remain agile while protecting the unique benefits that come from working side by side.
Interim Senior Clinical Scientist in London employer: Ellipses Pharma
Ellipses Pharma is an exceptional employer that fosters a collaborative and inclusive work culture, where face-to-face interaction is highly valued. With a strong focus on employee growth and development, the company offers opportunities to engage with leading Oncology experts while supporting a hybrid work model that promotes work-life integration. Joining Ellipses means being part of a dynamic team dedicated to advancing innovative oncology treatments in a supportive environment.
StudySmarter Expert Advice🤫
We think this is how you could land Interim Senior Clinical Scientist in London
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like Ellipses Pharma.
We think you need these skills to ace Interim Senior Clinical Scientist in London
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at Ellipses Pharma.
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at Ellipses Pharma. This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at Ellipses Pharma
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with Ellipses Pharma.
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help Ellipses Pharma achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
