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For Companies At a Glance
- Tasks: Lead scientific projects in clinical trials, focusing on medical imaging and data evaluation.
- Company: Join Perceptive, a pioneering company transforming clinical research in the biopharmaceutical industry.
- Benefits: Enjoy 25 days holiday, health cash plan, generous pension, and life assurance.
- Other info: Be part of an inclusive team dedicated to changing the world through science.
- Why this job: Make a real impact in healthcare by advancing innovative treatments and technologies.
- Qualifications: MD/PhD or MSc/BSc with relevant clinical research experience and strong communication skills.
The predicted salary is between 60000 - 80000 £ per year.
We’re on a mission to change the future of clinical research. At Perceptive, we help the biopharmaceutical industry bring medical treatments to the market, faster. Our mission is to change the world but to do this, we need people like you.
What can we offer you? Apart from job satisfaction, we can offer you:
- 25 days’ holiday (with the option to buy more)
- Health Cash Plan
- Optional private health, dental insurance, and health screens
- Cycle to work scheme
- Generous pension scheme with up to 10% employer contribution
- Life assurance
- Season ticket loan
About the role
Job Purpose
As a Principal Scientist, you will provide scientific input on projects for clinical trials where medical imaging and clinical data is used to evaluate efficacy and/or safety of investigational drugs or medical devices. In this role, you will work with the project team to lead all project related aspects of documents, application development and (where applicable) quantitative analysis workflow development, independently.
In addition, you will lead the development of image acquisition guidelines, medical documentation, preparation and conduct of external project team training, central reviewer training and reviewer quality control from a medical / scientific perspective in consultation with the relevant internal support and stakeholders.
Key Accountabilities
Document Development
Independently author internal and external facing documents and material such as:
- Standardized/Harmonized imaging parameters - Image Acquisition Guidelines (e.g. develop imaging parameters for specific clinical protocols to ensure standardization of imaging techniques in multi-center trials)
Document Review
Independently review and provide input to relevant project related documents such as:
- Project Plan
- Site Operations Manual, if requested
- Independent Review Charter
- Image QC and processing instructions (QC Form)
- Reviewer Manual, if applicable
- Clinical Data Transfer Instructions, if applicable
Prepare and conduct internal and external trainings
Independently create training material for and present to investigator sites, CRA and client (as needed) such as PowerPoint presentation, site guides on assessment criteria and imaging parameters. Independently create training material for and present to internal team on image acquisition parameters, quality control and image processing, e.g. image operations.
Support application development
Independently review requirement specifications of analysis application (including eCRF) and associated applications, and customization of relevant image viewing/analysis tools. Independently conduct User Acceptance Testing.
Participate in Independent Reviewer Selection
Review CVs of potential independent reviewers. Prepare and conduct Independent Reviewer Trainings.
Independently prepare and conduct Independent Reviewer Trainings, including:
- Prepare independent reviewer Training PowerPoint slides
- Review/Edit training associated documentation
- Select/Prepare training and testing cases for reviewer training
- Lead training of independent reviewers on the use of imaging software, analysis applications, and implementation of the review criteria
Independent Reviewer Performance Monitoring
Independently perform quality control and evaluation of the results of the independent review and provide necessary guidance and feedback to independent reviewers.
Quality
Identify non-compliances and non-conformances. Review audit findings, determine the risks associated with those findings and ensure that corrective actions are carried out.
Client Meetings
Participate in and significantly contribute to project related client meetings.
Communication
Effective and professional communication with internal and external stakeholders; acts as a translator as needed. Identify, evaluate, communicate and mitigate potential risks related to deliverables. Actively maintain and disseminate knowledge in one or more identifiable specialisms.
Functional Competencies (Technical knowledge/Skills)
- Ability to perform the tasks independently and able to work under own initiative
- Demonstrable ability to design and deliver training to a varied and global audience at all levels
- Demonstrable knowledge of medical terminology and practices
- Proven understanding of research methodologies and pragmatic application in a regulated environment
- Proven ability of using Microsoft Office products (including Word, Excel & PowerPoint)
- Excellent interpersonal, verbal and written communication skills
- A flexible attitude with respect to work assignments and new learning
- Ability to manage multiple and varied tasks with enthusiasm and prioritise workload with attention to detail
- Must have the ability to work methodically in a fast-paced, time-sensitive environment
- Demonstratable ability to apply critical thinking to problems and tasks
- Ability to identify and implement process improvements
- Proactively participates in skills improvement training and encourages their teams to participate
- Maintain an up-to-date awareness of trends, tools, technology, techniques, processes and developments within the Life sciences domain
Knowledge & Experience
- MD/PhD with relevant Clinical Research experience OR MSc with considerable experience OR BSc / Undergraduate degree in Nursing / Technologist Certification with substantial experience in imaging or clinical trials
- Solid proven experience of working in and knowledge of medical imaging or clinical development in the life sciences industry and regulated environments.
- Experience using tools to communicate progress to stakeholders.
- English: Fluent
Come as you are. We're proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, colour, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Principal Scientist, Radiopharmaceutical Therapy employer: Perceptive
Contact Detail:
Perceptive Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Scientist, Radiopharmaceutical Therapy
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Understand their mission and values, and think about how your skills as a Principal Scientist can contribute to their goals. Show them you’re not just another candidate!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. Focus on articulating your experience in clinical research and how it aligns with the role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive and engaged with our mission.
We think you need these skills to ace Principal Scientist, Radiopharmaceutical Therapy
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Principal Scientist role. Highlight your relevant experience in clinical research and medical imaging, and show us how you can contribute to our mission at Perceptive.
Showcase Your Skills: Don’t forget to emphasise your technical skills and experience with document development and training. We want to see how you can lead projects and communicate effectively with both internal teams and clients.
Be Clear and Concise: When writing your application, keep it clear and to the point. Use straightforward language and avoid jargon unless it's necessary. We appreciate a well-structured application that’s easy to read!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Perceptive
✨Know Your Stuff
Make sure you brush up on your medical imaging and clinical research knowledge. Be ready to discuss specific methodologies and how they apply to the role of Principal Scientist. Familiarise yourself with recent trends in radiopharmaceutical therapy to show you're on top of your game.
✨Prepare for Document Development Questions
Since you'll be authoring and reviewing various documents, think about examples from your past experience where you've successfully developed or reviewed similar materials. Be prepared to explain your thought process and how you ensure quality and compliance in your work.
✨Show Off Your Training Skills
You'll need to create and deliver training materials, so come prepared with examples of training sessions you've conducted. Highlight your ability to communicate complex information clearly and effectively, especially to diverse audiences.
✨Engage with the Interviewers
Don't just answer questions—engage in a conversation! Ask insightful questions about the company's projects and culture. This shows your genuine interest in the role and helps you assess if it's the right fit for you too.