At a Glance
- Tasks: Lead clinical trials in Alzheimer's research and provide expert guidance on cognitive assessments.
- Company: Join Clario, part of Thermo Fisher Scientific, transforming lives through innovative research.
- Benefits: Competitive pay, private health, flexible time off, and modern tech for remote work.
- Other info: Dynamic role with opportunities for international travel and career growth.
- Why this job: Make a real impact in neurodegenerative disease research and help develop life-changing therapies.
- Qualifications: Graduate degree in Life Sciences or related field with clinical research experience.
The predicted salary is between 40500 - 49500 £ per year.
Join Clario, a part of Thermo Fisher Scientific and help advance clinical research through innovative electronic Clinical Outcome Assessment (eCOA) solutions that support the development of life-changing therapies worldwide. As a Clinical Scientist, you will serve as a trusted scientific partner to sponsors, investigative sites, and internal stakeholders, with a primary focus on Alzheimer's disease (AD), dementia, and other neurodegenerative disorder clinical research programs. You will ensure the successful delivery of scientific services across global clinical trials while providing expert guidance on cognitive endpoints, clinical outcome assessments, and rater quality initiatives supporting innovative therapies for patients affected by neurodegenerative diseases.
What We Offer
- Competitive compensation and incentives.
- Private health, pension, and life insurance.
- Flexible time off and hybrid work.
- Engaging employee programs.
- Modern technology for remote collaboration.
What You'll Be Doing
- Serve as the primary scientific contact for assigned international clinical trials, providing scientific leadership and expertise to sponsors, investigative sites, and internal stakeholders.
- Co-lead study execution alongside Project Management teams, ensuring scientific integrity, operational excellence, and successful project delivery.
- Participate in and lead sponsor meetings, investigator meetings, scientific discussions, and cross-functional project reviews.
- Monitor study performance metrics and develop meaningful analyses, dashboards, and reports highlighting trends, risks, outliers, and mitigation strategies.
- Identify and resolve clinical quality, endpoint quality, and data integrity issues in accordance with study requirements and Good Clinical Practice (GCP).
- Develop and deliver rater training, calibration activities, and remediation programs aligned with study-specific requirements.
- Provide scientific consultation and support regarding clinical outcome assessments, cognitive and functional endpoints used in Alzheimer's disease and dementia research, study design considerations, endpoint strategy, and protocol implementation.
- Provide therapeutic-area expertise in Alzheimer's disease, dementia, and related neurodegenerative disorders, supporting study design, endpoint strategy, rater training, data quality review, and sponsor consultations.
- Respond to sponsor inquiries related to scoring methodologies, endpoint quality, scientific interpretation, and study conduct.
- Coordinate cross-functional activities to ensure project milestones, deliverables, and scientific objectives are achieved.
- Support the development and review of study materials, including electronic forms, training content, endpoint documentation, scale verification activities, and scientific guidance materials.
- Contribute scientific expertise to feasibility assessments, proposal development, and business development activities.
- Establish and maintain strong relationships with sponsors, investigators, consultants, key opinion leaders, and clinical research professionals.
- Participate in scientific research initiatives and contribute to publications, conference presentations, and other scientific dissemination activities.
- Support the development and continuous improvement of SOPs, work instructions, training materials, and operational processes.
- Maintain awareness of evolving industry trends, clinical research methodologies, regulatory requirements, and therapeutic area advancements relevant to assigned studies.
What We Look For
- Graduate degree in Life Sciences, Psychology, Neuroscience, Clinical Research, Public Health, Pharmacy, or a related scientific discipline.
- Minimum of 5 years of experience within the clinical research industry, preferably within a CRO, biopharmaceutical, healthcare, or related environment.
- At least 3 years of experience in a Clinical Scientist, Clinical Trial Science Lead, Medical Science, or other client-facing scientific role.
- Minimum of 4 years of experience supporting the administration, training, or oversight of clinical outcome assessments, rating scales, or study endpoints.
- Demonstrated expertise in Alzheimer's disease, dementia, and/or other neurodegenerative disorders through clinical research, therapeutic area specialization, patient population experience, endpoint development, or scientific leadership.
- Comprehensive understanding of clinical trial methodology, study execution, scientific principles, and endpoint quality management, including cognitive and functional outcome measures commonly utilized in AD and dementia clinical research.
- Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and clinical research regulations.
- Understanding of research methods, data interpretation, and applied statistics.
- Proven ability to manage multiple studies, priorities, and stakeholder relationships in a dynamic global environment.
- Strong leadership skills with the ability to influence, collaborate, and drive outcomes across cross-functional teams.
- Excellent verbal and written communication skills, including experience presenting to sponsors, investigators, and large audiences.
- Fluency in English; additional language skills are advantageous.
- Willingness and ability to travel internationally approximately 10-20% as business needs require.
- Strong problem-solving, critical thinking, organizational, and stakeholder management skills.
At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.
Clinical Scientist, Neuroscience (Alzheimer's Disease & Dementia) employer: Clario
Clario, part of Thermo Fisher Scientific, is an exceptional employer that prioritises employee well-being and professional growth. With competitive compensation, flexible working arrangements, and a strong focus on work-life balance, we foster a collaborative culture where your contributions directly impact patient outcomes globally. Join us to be part of a team that values innovation and supports your career development in the dynamic field of medical writing.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Scientist, Neuroscience (Alzheimer's Disease & Dementia)
✨Get Involved with Local Health Initiatives
Join local community health events or volunteer for organisations like public health agencies. This not only builds your experience but also helps you network with industry professionals who might know of openings at places like Clario.
✨Tap into Professional Associations
Check out associations like the Institute of Healthcare Management. They often have job boards, networking events, and conferences that are perfect for connecting with potential employers in health sciences administration.
✨Stay Updated with Industry Trends
Follow health policy news and trends—being knowledgeable about the current landscape will not only help you in interviews but also make you stand out as a candidate. You can discuss recent developments and their implications when chatting with folks at Clario.
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We think you need these skills to ace Clinical Scientist, Neuroscience (Alzheimer's Disease & Dementia)
Some tips for your application 🫡
Highlight Your Relevant Experience:When applying for a role in health sciences administration, it's super important to spotlight any relevant experience you have in healthcare settings. Whether you've worked in a hospital, a clinic, or any related environment, make sure to detail those roles in your CV – focusing on your responsibilities and achievements that align with the job at Clario.
Showcase Your Administrative Skills:Administrative skills are key in this field, so don’t hold back! Make sure your CV reflects your proficiency in things like scheduling, data management, and compliance with health regulations. Mention specific software you’ve used, such as patient management systems, as this will demonstrate your hands-on abilities and readiness for the role at Clario.
Craft a Meaningful Cover Letter:Your cover letter should reflect your passion for the health sciences field and your eagerness to contribute to Clario. Share a bit about why you’re drawn to this sector, any impactful situations or challenges you’ve encountered, and how they’ve shaped your desire to work in health sciences administration. This personal touch can really set you apart!
Tailor Your Documents to the Job:Don't use a one-size-fits-all approach! Make sure your CV and cover letter are specifically tailored for this role. Highlight any certifications you have relevant to health administration, and ensure you clearly connect your previous roles to the skills needed for the full-time position at Clario. This way, you're showing them you’ve done your homework and are genuinely interested in being a part of their team.
How to prepare for a job interview at Clario
✨Showcase Your Administrative Skills
In health sciences administration, being organised is key. Make sure you can demonstrate your skills in managing schedules, paperwork, and data accurately. Be ready to discuss specific tools you've used, like electronic health record systems or scheduling software, and how they improved efficiency in your past experiences.
✨Know Your Regulations
Familiarity with healthcare regulations and compliance is crucial. Brush up on HIPAA, GDPR, or other relevant policies before your interview. We recommend preparing examples of how you've ensured compliance or handled sensitive information in past roles—this will show you're not just knowledgeable but also responsible.
✨Prepare for Scenario Questions
Interviews for administrative roles often involve scenario-based questions to assess your problem-solving skills. Practice responses to common situations you might face, such as dealing with a challenging patient or managing a sudden schedule change. This will not only demonstrate your ability to think on your feet but also highlight your interpersonal skills.
✨Align Your Goals with the Organisation
As a full-time candidate, employers will want to know how your long-term career goals align with their mission. Take some time to research Clario’s values and be ready to tie your passion for health sciences administration into their objectives. Demonstrating enthusiasm and career alignment can be a game-changer in this competitive field!