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DEINE MISSION BEI UNS Gestalte die Zukunft der Schmerztherapie mit uns! In dieser Rolle sorgst Du für höchste Qualitätsstandards in unseren klinischen Studien....
Gestalte die Zukunft der Schmerztherapie mit uns! In dieser Rolle sorgst Du für höchste Qualitätsstandards in unseren klinischen
Studien. Du gestaltest unser Clinical Quality Assurance System aktiv mit, erkennst Risiken frühzeitig und stellst die Einhaltung
regulatorischer Anforderungen sicher. In enger Zusammenarbeit mit internen Teams und externen Partnern treibst Du Verbesserungen
voran und sorgst dafür, dass Qualität konsequent umgesetzt wird. Bereit, Verantwortung zu übernehmen und wirklich etwas zu
bewegen? Dann suchen wir genau Dich!
Non-Compliances an Studienzentren
Non-Compliances durch die Entwicklung von CAPA-Maßnahmen
Vertanical ist ein weltweit führendes Biopharmaunternehmen, das sich auf die Entwicklung und den Vertrieb innovativer Arzneimittel
zur Behandlung chronischer Schmerzen spezialisiert hat. Dabei verfolgen wir eine klare Vision: Eine Welt frei von chronischen
Schmerzen! Mit VER-01 haben wir ein einzigartiges cannabinoidbasiertes Arzneimittel zur Behandlung chronischer Schmerzen
entwickelt, das im Juni 2026 unter dem Namen Exilby in Deutschland und Österreich zugelassen wurde. Damit haben wir nach mehr als
acht Jahren intensiver Forschungs- und Entwicklungsarbeit einen bedeutenden Meilenstein erreicht.
Die Zulassung in den USA ist für 2029 geplant. Unser Ziel ist es, Exilby bis 2030 als führende Therapie zur Behandlung chronischer
Schmerzen zu etablieren und damit neue Maßstäbe in der Schmerztherapie zu setzen.
Für Dich klingt das spannend? Dann bewirb Dich jetzt!
Wir bieten Dir einen vielfältigen, anspruchsvollen Job mit spannenden Aufgaben und einem breiten Spektrum an
Gestaltungsmöglichkeiten! Unser innovatives Umfeld ermöglicht Dir Deine berufliche Entfaltung mit kurzen Entscheidungswegen,
Verantwortung von Tag 1 an und den Freiraum, neue Wege zu gehen. Auf Dich wartet individuelles Learning und echte Sinnhaftigkeit –
schenke mit Deinem persönlichen Beitrag Millionen von Menschen ein neues Leben!
Bewirb Dich jetzt! Wir freuen uns darauf, Dich kennenzulernen.
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ABOUT US: Spectrum.Life is a whole-of-health digital partner that guides organisations and their people to thrive, delivering clinically backed digital health, mental health and wellbeing solutions. Our HealthTech delivers digital transformation for Insurers, Educators and Employers through Co-creation or seamlessly integrated out-of-the-box solutions, that decrease digital fragmentation and engage, empower, and transform their people’s lives. Established in 2018 by Stuart McGoldrick and Stephen Costello, Spectrum.Life provides services internationally to over 7.2m insurance members, 3,000 corporate clients, 60 universities and 650,000 university students. Spectrum.Life currently employs over 450 people. Our vision is to change and save as many lives as possible. ROLE BRIEF: Why This Role Matters Waiting lists for neurodiversity assessments in the UK are long — often years. For autistic people and those with ADHD, that wait is not just frustrating. It affects education, employment, relationships, and mental health. At Spectrum.Life, we are building a digital-first neurodiversity multi-disciplinary assessment service that is clinically rigorous, neuroaffirmative in its values, and genuinely accessible. We are looking for a Practitioner Psychologist who shares that commitment — someone who brings both the specialist technical competence this work demands and a genuine belief in the difference that timely, high-quality identification can make to a person’s life. This is a fully remote, multidisciplinary role. You will be part of a team of psychologists, Speech and Language Therapists, and Occupational Therapists, working together to deliver integrated, person-centred assessments for children aged seven and above and adults. The Neurodiversity Assessment Service Spectrum.Life’s Neurodiversity Assessment Service delivers high-quality Autism, ADHD, and combined AuDHD identification assessments for children (aged seven and above) and adults, fully remotely via virtual platforms. All assessments are conducted in line with NICE guidelines and within DSM-5 and ICD-11 diagnostic frameworks. Our approach is neuroaffirmative throughout — from the way we conduct initial consultations to the language we use in our reports and feedback sessions. We work from a strengths-based, person-centred model that respects individual identity and lived experience. This is a growing service, and you will have the opportunity to contribute directly to its development — including service design, quality improvement, and the way we use digital platforms to make assessments more accessible. Your Multidisciplinary Team Neurodiversity assessment is inherently multidisciplinary, and we have built the service to reflect that. You will not be assessing in isolation. Your MDT includes Practitioner Psychologists, Speech and Language Therapists, and Occupational Therapists. Each assessment integrates perspectives across all three disciplines, and integrated formulation is a core part of how we work — not an add-on. How the MDT works day to day * Regular MDT formulation meetings where complex and combined presentations are discussed collaboratively across psychology, SLT, and OT * Shared formulation on all assessments — your psychological assessment report is integrated with SLT and OT findings before the final report is produced * A designated Clinical Manager who provides operational oversight and is available for clinical consultation * Monthly individual clinical supervision from a specialist in neurodiversity — provided by an experienced senior clinician with specialist neurodiversityexpertise, not generic CPD supervision * Peer consultation and shared learning across the psychology team * Clear safeguarding and escalation pathways, with governance support for complex or high-risk presentations SCHEDULE: This is a 32-hour per week permanent part-time role. We will discuss and agree your specific working pattern during the offer process — we want to find a schedule that works for you within the needs of the service. The role is fully remote. All assessments and MDT meetings are conducted virtually. You will need access to a private, confidential workspace and a reliable internet connection. RESPONSIBILITIES: Neurodiversity Assessments * Deliver high-quality, neuroaffirmative Autism and ADHD identification assessments for children (aged seven and above) and adults through virtual platforms,in accordance with NICE guidelines * Administer, score, and interpret the ADOS-2 and ADI-R, as well as validated ADHD assessment measures * Conduct thorough initial neurodiversity consultations, clarifying presenting concerns, priorities, and individual goals in a collaborative, person-centred manner * Complete comprehensive biopsychosocial and multidisciplinary formulations, integrating developmental history, observation, standardised assessment, and collateral information * Produce high-quality written assessment reports that present complex clinical information clearly, accessibly, and in a strengths-based manner — suitable for individuals, families, and professional stakeholders * Deliver clear, sensitive, and neuroaffirmative feedback sessions to individuals and families following assessment completion * Identify and communicate relevant reasonable accommodations across educational, workplace, and community settings Caseload and Clinical Responsibilities * Hold a designated caseload, acting as lead practitioner and guiding clients through their assessment journey from initial consultation to post-diagnostic support * Undertake risk screening and safeguarding assessments in line with relevant UK legislation and organisational procedures, with particular attention to children and young people * Provide formulation-led post-diagnostic psychological support, where indicated by clinical need — this is distinct from an ongoing therapy caseload and is focused on understanding and applying assessment findings * Liaise with external agencies including education, health, and social care services asrequired MDT Collaboration and Service Development * Collaborate closely with SLT and OT colleagues to ensure integrated, person-centred assessment formulations * Support the Clinical Manager in outcomes monitoring, quality assurance, and clinical governance activities * Contribute to service development, audit, and quality improvement as the neurodiversity service grows * Provide consultation and, where appropriate, training on neurodiversity to families, schools, or other professionals REQUIREMENTS: Registration and Qualification Requirements Both of the following are mandatory for appointment to this role: * Doctoral qualification in Psychology (Clinical, Counselling, or Educational) * Current registration with the Health and Care Professions Council (HCPC) as a Practitioner Psychologist * Chartered Psychologist status with the British Psychological Society (BPS) Why both HCPC registration and BPS Chartership are required HCPC registration is the statutory requirement for practising as a Practitioner Psychologist in the UK. BPS Chartership provides the additional professional assurance expected for the complexity of neurodiversity assessment work in this service — particularly in relation to ADOS-2 and ADI-R administration, multidisciplinary formulation, and report writing for diagnostic purposes. Both are required for the appointment. * Minimum two years of post-HCPC registration experience, including direct neurodiversity assessment experience * Formal training anddemonstratedcompetence in ADOS-2 administration and interpretation * Formal training and demonstrated competence in ADI-R administration and interpretation Essential Experience and Knowledge Assessment Experience * Experience conducting neurodiversity assessments across the lifespan, with awareness of age-related presentation differences * Experience producing comprehensive neurodiversity assessment reports, including recommendations and reasonable accommodations * Experience providing post-diagnostic feedback to individuals and families * Experience working as part of a multidisciplinary assessment team * Experience of biopsychosocial and systemic formulation of neurodevelopmental presentations * Experience delivering remote or virtual assessments to children (aged seven and above) and/or adults Clinical Knowledge * Strong knowledge of NICE guidelines relevant to Autism (NG142, NG228) and ADHD (NG87) * Knowledge of DSM-5 and ICD-11 diagnostic criteria for Autism and ADHD * Knowledge of co-occurring conditions (anxiety, learning disabilities, developmental trauma) and their interaction with neurodevelopmental presentations * Knowledge of reasonable adjustments legislation (Equality Act 2010) and application in educational and workplace settings * Knowledge of safeguarding and risk frameworks relevant to children, young people, and adults in the UK DESIRABLE: * Experience assessing combined AuDHD presentations * Experience adapting assessments for individuals with co-occurring intellectual disabilities, sensory needs, or complex communication profiles * Experience providing clinical supervision to more junior staff * Knowledge of SpLD frameworks (dyslexia, dyspraxia/DCD) and their interaction with neurodevelopmental conditions * Experience working across NHS and independent sector pathways * Experience contributing to service development, audit, or quality improvement WHAT ARE THE BENEFITS OF WORKING AT SPECTRUM.LIFE? * Clinical environment — what you can rely on Monthly individual supervision from a specialist neurodiversity clinician. Regular MDT formulation meetings. Peer consultation and shared learning across the psychology team. Clinical governance and safeguarding support. Full training on remote assessment protocols and digital platforms before your first case. * Part-time permanent contract at 32 hours per week * Competitive salary (dependent on experience) * Fully remote working * 25 days annual leave * 24/7 EAP and a wide range of health and wellbeing supports * CPD funding and access to specialist training, including support to maintain and develop ADOS-2 and ADI-R competencies * The opportunity to practise in a genuinely neuroaffirmative service and contribute to meaningful change in how neurodiversity is understood and supported * The chance to shape a growing, digital-first neurodiversity service from an early stage * Training and continuing professional development opportunities, including specialist neurodiversity assessment tools
THE ROLE At Quotient Sciences, we're redefining the way medicines are developed by bringing together drug development and clinical testing under one integrated model. As we continue to grow our clinical capabilities, we have an exciting opportunity for an experienced Senior Clinical Research Associate to help build and shape our clinical monitoring function. This is a unique role for a senior clinical research professional who wants to do more than deliver monitoring activities. You'll play a key part in establishing monitoring standards, driving inspection readiness, influencing future operating models and supporting the growth of our clinical monitoring capability across both healthy volunteer and patient studies. Working closely with Clinical Operations, Quality Assurance and study teams, you'll ensure that studies are conducted to the highest standards of quality, compliance and participant safety. You'll also have the opportunity to mentor future CRA talent and contribute to the development of a best-in-class monitoring service. If you're looking for a role where you can combine hands-on monitoring expertise with strategic influence and leadership, we'd love to hear from you. KEY RESPONSIBILITIES * Lead clinical monitoring activities across Phase I healthy volunteer studies and early phase patient trials. * Conduct site qualification, site initiation, routine monitoring and close-out visits. * Ensure participant safety, protocol compliance and data integrity throughout the clinical trial lifecycle. * Prepare, review and submit monitoring documentation, visit reports and follow-up letters within agreed timelines. * Identify, document and follow up on protocol deviations, GCP findings and corrective actions. * Support investigators and study teams to resolve monitoring findings and compliance issues. * Oversee the collection and maintenance of essential study documentation to ensure inspection readiness. * Perform drug accountability oversight activities and support risk-based monitoring approaches. * Act as a monitoring lead across studies and serve as a key contact for internal teams, external sites and CRO partners. * Help establish and continuously improve monitoring processes, quality standards and working practices. * Define and track monitoring KPIs and quality metrics, providing updates to study and leadership forums. * Contribute to the recruitment, onboarding and mentoring of future CRA team members. * Support GCP training, inspection readiness activities, audits and regulatory inspections. * Work collaboratively with Quality Assurance and Clinical Operations to drive continuous improvement across clinical trials. SKILLS AND EXPERIENCE REQUIRED ESSENTIAL * Degree in Life Sciences, Nursing, Healthcare or a related discipline, or equivalent experience. * Minimum of 5 years' Clinical Research Associate experience within a pharmaceutical, biotechnology or CRO environment. * Proven independent on-site monitoring experience. * Strong knowledge of ICH-GCP and applicable UK, EU and international regulatory requirements. * Experience supporting Phase I and/or early phase patient clinical trials. * Experience managing monitoring documentation and site activities across the study lifecycle. * Excellent organisational skills with the ability to manage multiple priorities effectively. * Strong communication and stakeholder management skills, with the confidence to challenge constructively when required. * Ability to work independently, make sound decisions and solve complex problems. DESIRABLE * Experience supporting regulatory inspections and audits. * Experience mentoring, coaching or developing junior CRA colleagues. * Experience helping establish or enhance clinical monitoring processes or functions. * Experience working with IWRS/IRT and ePRO systems. * Experience working within sponsor and CRO partnership models. * Experience developing monitoring KPIs, quality measures or performance metrics. LEARNING OPPORTUNITIES * Play a leading role in building and shaping Quotient Sciences' clinical monitoring capability. * Influence monitoring strategy, quality standards and future operating models. * Develop leadership and mentoring experience within a growing function. * Work across a diverse portfolio of Phase I and early phase clinical studies. * Collaborate with experts across Clinical Operations, Quality Assurance and Regulatory disciplines. * Gain exposure to innovative drug development programmes and integrated clinical research delivery. * Contribute to inspection readiness initiatives and continuous improvement projects that have a lasting impact across the organisation. This role offers a rare opportunity to combine hands-on clinical monitoring expertise with the chance to influence how monitoring is delivered within a growing and evolving organisation. If you're passionate about quality, compliance and clinical research excellence, we'd love to hear from you.
About myTomorrows myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options. We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem. We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection. With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business. Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today. The opportunity: Backend Engineer As a Backend Engineer, you will be responsible for developing and maintaining the platform infrastructure that powers our products. You will work closely with our Frontend Engineers, DevOps Engineers, and other stakeholders to design and build scalable, reliable, and high-performance products. Given that most of our team is located in the Netherlands, we only consider candidates for this position who live within commuting distance to our office in Amsterdam. What you'll do in this role: * Design and implement scalable and reliable backend systems and infrastructure to support our products * Develop and maintain our micro-services to expose platform functionality to internal and external clients * Collaborate with development and quality assurance teams to ensure high availability, scalability, and security of our systems * Collaborate with DevOps Engineers to ensure the continuous delivery and deployment of software products * Work with software developers to identify and implement improvements to our platform architecture and functionality * Develop and maintain documentation of our systems and processes * Mentor and train junior members of the backend team * Keep up-to-date with the latest trends and technologies What you bring to the table: * Proficiency in Python programming language * 3+ years of experience in the related field * Experience with relational databases such as MySQL, PostgreSQL, or Oracle * Experience with the cloud platforms (AWS, Azure or GCP) * Experience with containerization technologies such as Docker and Kubernetes * Excellent problem-solving skills and ability to work independently and as part of a team * Strong communication skills and the ability to work with stakeholders across the organization * Excellent English communication skills WHAT SUCCESS IN THE FIRST 6 MONTHS LOOKS LIKE: * You’ve built trust with Product, Frontend, and DevOps peers and taken clear ownership of 2-3 domain APIs/services, including stewardship of their contracts and SLAs. * You’ve established an API-first workflow: starting from use cases, you propose and socialize OpenAPI specs, align on naming and conventions, then implement in FastAPI with Pydantic models. * You’ve delivered impactful API features end-to-end (design → implementation → tests → docs) that are consumed by internal and external clients without hand-holding. * You’ve raised API robustness: strong request/response validation, consistent error models, pagination and idempotency where appropriate, and backward-compatible versioning enforced via automated contract tests in CI (ruff, Poetry, pre-commit). * You’ve improved the reliability and performance of our service by adding meaningful observability (metrics, logs, tracing) and defining SLIs/SLOs for key endpoints—reducing 5xx rates and improving p95 latency. * You’ve made safe database changes in MySQL with SQLAlchemy migrations, optimized critical queries, and contributed to data access patterns involving DynamoDB or Neo4j while keeping API contracts stable. * You’ve strengthened the security of APIs (authN/authZ boundaries, scoped tokens, least-privilege access, secrets management, rate limiting) and documented the approach. * You’ve written clear API documentation and examples (e.g., snippets/collections), shared knowledge with the team, and mentored junior engineers so others can build on your work. Current tech stack: We are fully cloud-native, leveraging AWS and adopting a Lean, API-first product development approach driven by modern cloud technologies and thoughtful design practices. Our backend applications are built using Python, FastAPI, Pydantic, and SQLAlchemy (MySQL). On the front end, we predominantly develop with Angular and also utilize Headless Wagtail and WordPress for select products. To ensure code quality and a consistent release pipeline, we employ GitHub Actions for CI/CD along with tools like Renovate, ruff, Poetry, and pre-commit. We containerize our applications using Docker and Docker Compose. Currently, we are transitioning from AWS Lambda-based deployments to Kubernetes-managed services and moving from AWS CloudFormation to Terraform for infrastructure as code. We continue to expand our capabilities in knowledge graphs (Neo4j) and database technologies (MySQL, DynamoDB). What we offer: * Impactful work that helps patients gain access to potentially lifesaving treatments. * International work environment, scale-up energy and a flat organizational structure that encourages creativity and accountability. * Competitive salary, annual performance bonus and an Employee Stock Option Plan. * Great career development opportunities in a fast-growing company. * Learning and development budget alongside internal knowledge sharing sessions. * Attractive pension plan, full premium covered by myTomorrows. * Hybrid working model. * Policies to support working parents. * Healthy lunch at the thriving Amsterdam office. * Unlimited access to professional guidance by certified psychologists via OpenUp * Enjoy monthly events hosted by our vibrant Culture Club as well as an annual ‘myTomorrowland’ company-wide celebration! Equal opportunities myTomorrows is an Equal Opportunity Employer and, beyond upholding discrimination-free practices, we are committed to cultivating a workplace where difference and diversity are protected and celebrated. The best work comes from our best selves, and we go to great lengths in supporting our team members to be just that.