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Córdoba, ES
Veterinario/A De Campo – Reproducción Y Clínica Bovina
Organización Colegial Veterinaria · Córdoba, ES
.
Un centro veterinario de servicios integrales en Córdoba busca un veterinario/a de campo para realizar trabajos de reproducción y clínica en vacuno de leche y carne.
Se ofrece un ambiente de trabajo dinámico y oportunidades de crecimiento profesional dentro de un equipo consolidado y con excelentes medios técnicos.
La compensación se determinará según la experiencia y el grado de implicación del candidato.
Interesados/as deben enviar su currículum a ******.
#J-*****-Ljbffr
Let's Health
Clinical / Medical Director
Let's Health · Chantada, ES
Teletreball .
We're looking for a Medical Affairs Director!
Are you passionate about shaping global Medical Affairs strategy and driving scientific excellence in healthcare?
At Let's Health, we're growing and looking for aMedical Affairs Directorto lead high-impact strategic initiatives with global biopharma clients.
This role combines scientific leadership, client partnership, and innovation, positioning you as a key member of our leadership team, reporting directly to our CEO.
______________________________________________________________________________
About Let's Health
We only do one thing: help life sciences companies launch and grow their brands.
That takes medical strategy, creative excellence, and sharp technological execution working as one.
We don't collaborate.
We partner.
For 18+ years, we've partnered with the world's leading biopharma companies to turn complex evidence into strategy, content, and campaigns that actually land with HCPs, patients, and decision-makers.
We work across 25+ markets, with 150+ biopharma clients who keep coming back.
And right now, we're in a real growth moment, building the team and the infrastructure to take things to the next level.
If you want to do meaningful work in healthcare, in a place small enough that your contributions genuinely matter, this might be exactly what you're looking for.
______________________________________________________________________________
Your Mission
You will act as thesenior scientific partnerfor our key clients, leading Medical Affairs strategy across the full product lifecycle.
You will translate complex science into actionable strategies, guide global engagements, and strengthen Let's Health's position as a trusted scientific and strategic advisor.
You will also play a critical role inbusiness growth, and innovationworking closely with the CEO and cross-functional teams to evolve our Medical Affairs offering.
______________________________________________________________________________
Key Responsibilities
- Medical Affairs Strategy Design & Planning
Develop structured strategic frameworks and playbooks translating scientific and business priorities into execution.
Act as a strategic advisor to senior stakeholders, ensuring cross-functional alignment.
- Insight Generation & Strategic Integration
Translate insights into clear strategic recommendations directly informing brand and medical decision-making.
- Evidence Translation & Field Enablement
Enable in-field and global teams to deliver consistent, high-impact scientific engagement, bridging the gap between data and execution.
Ensure compliance with global regulatory standards (EFPIA and equivalents).
- KOL Engagement & External Scientific Leadership
Represent Let's Health externally as senior scientific leader and trusted partner.
- Congress & Scientific Events Strategy
Ensure effective post-event insight capture, competitive intelligence, and dissemination to maximize strategic impact.
- Scientific Education, Communication & Content Excellence
Ensure clarity, consistency, and compliance, while driving innovation in scientific communication.
- Training & Capability Building
Equip teams with the knowledge, tools, and capabilities required to execute effectively and engage stakeholders with confidence.
______________________________________________________________________________
What You Bring
Advanced degree in Medicine, Pharmacy, Life Sciences, or related field (PhD/MD preferred).
Extensive experience in Medical Affairs within pharma, MedTech, or healthcare consulting.
Proven track record managing senior client relationships at global level.
Strong strategic thinking and ability to translate science into business impact.
Experience leading multidisciplinary teams and complex international projects.
Deep understanding of regulatory frameworks and compliance standards.
Fluency in English (and ideally also Spanish[GN1] ) with excellent communication and presentation skills
______________________________________________________________________________
What We Offer
A leadership role with high strategic impact in a fast-growing international company.
Collaboration with leading global pharmaceutical companies.
The opportunity to shape the future of Medical Affairs and Let's Health.
A dynamic, innovation-driven, and collaborative work environment in Madrid with up to two remote working days per week.
A culture built on trust, scientific excellence, and continuous development.
A competitive package that values what you bring to the table.
Want to know more?
Send your CV ******.
Clínicas Tulaser
Orihuela, ES
TÉCNICO ESTETICISTA EN CLÍNICAS TULASER ORIHUELA
Clínicas Tulaser · Orihuela, ES
.
Clínicas Tulaser es una empresa en constante crecimiento que tiene como misión acercar los servicios profesionales de depilación láser indolora a todo el mundo y ofrecer tratamientos faciales, corporales y de medicina estética. Cuenta con clínicas en toda España a nivel nacional e internacional.
-Buscamos incorporar un/a Técnico Esteticista especializada en realización de tratamientos de depilación láser y aparatología facial y corporal para nuestra clínica ubicada en Avenida Teodomiro, Orihuela
Se ofrece:
-25 horas semanales.
-Contrato temporal (con posibilidad de indefinido)
-Turno de tardes de Lunes a Viernes y 1 sábado al mes.
-Incorporación inmediata.
-Salario fijo + importantes comisiones
-Formación continua incluida en aparatología de última generación, protocolos de trabajo y ventas
Tareas
-Elaboracion de presupuestos.
-Venta y asesoramiento del cliente.
-Realización y asesoramiento de Tratamientos Faciales con Aparatología de última generación como Hifu, Diatermia, Fototerapia, Mesofrecuencia,…
-Asesoramiento y Realización de tratamientos Corporales: Remodelación Corporal, Reafirmación, Desarrollo Muscular, etcc..
Trabajamos con Sculptor, Diatermia, Hifu, Mesofrecuencia entre otros tratamientos.
- Depilación Láser Shr Sin Dolor con aparatología de última generación.
Requisitos
-Experiencia como comercial esteticista minimo 2 años.
-Personalidad dinámica y proactiva.
-Hablidades comerciales y empatía.
-Formación reglada.
-Experiencia en el puesto mínimo de un año en aparatología estética.
-Que le guste trabajar por objetivos.
Beneficios
-Posibilidad de crecimiento y desarrollo.
-Estabilidad laboral.
-Buen ambiente laboral y trabajo en equipo
Si crees que puedes encajar en nuestro equipo no dudes en aplicar la oferta, ¡estamos deseando conocerte!
Podólogo
NovaClínica del Pie Marta García
Albacete, ES
Podólogo
Clínica del Pie Marta García · Albacete, ES
.
Descripción de la empresa
En Clínica del Pie Marta García, situada en Albacete, nos dedicamos al cuidado integral de la salud de los pies.
Nuestro compromiso es ofrecer un servicio de alta calidad basándonos en la profesionalidad y una atención personalizada.
Nos esforzamos en crear un entorno en el que la salud y el bienestar de nuestros pacientes sean siempre nuestra prioridad.
Qué buscamos
Experiencia mínima de 3 años en consulta
Profesional responsable, cercana y con buena actitud
Capacidad de trabajo en equipo
Se valorarán los cursos de formación y experiencia en biomecánica
Qué ofrecemos
Buen ambiente de trabajo ??
Incorporación a una clínica moderna y en crecimiento
Condiciones a valorar según experiencia
Si te gusta tu profesión, te implicas con tus pacientes y quieres formar parte de nuestro equipo... ¡queremos conocerte!
- Envíanos tu CV a ******
Legit.Health
Life Science Project Manager (Clinical Trials & Healthcare Projects For Samd)
Legit.Health · Pontevedra, ES
Teletreball . Javascript PHP Python ERP Office
About us Legit.Health deploys computer vision and artificial intelligence technology to enable lifesaving diagnosis and therapies for visible diseases.
Our goal is to enable universal access to high-quality diagnosis and follow-up of pathologies and to offer affordable health assistance to everyone everywhere.
Things you should know before following and signing up for the position: We are a startup, it is important that you are knowledgeable about how startups operate and know that at this stage there are more unknowns than certainties.
There are many things to discover and define yet, so you will be part of that definition, therefore you will have many functions helping the management.
At Legit.Health we have a friendly open collaborative culture and a united team vision.
We love entrepreneurial/risk taking/high ambition mindsets.
Our work is rewarding and we help each other win by creating a supportive and collaborative environment for one another.
Take a look at our opening below and send us your application - we look forward to hearing from you!
Job description We are on the lookout for a passionate Life Science Project Manager with a focus on clinical trials and healthcare innovation and a specialization in software medical devices , eager to drive innovation in the evolving landscape of digital health.
This pivotal role involves leading the development and implementation of transformative projects in healthcare technology from conception to delivery .
The ideal candidate will bridge the gap between commercial, clinical and technical teams , translating customer needs into actionable specifications , and ensuring our solutions not only meet the high standards required by our health sector partners and their patients but also stay within budget and time constraints while adhering to regulatory requirements.
A key part of your role will be working with partners (hospitals, CROs, and research institutions), ensuring proper study design, execution, and integration of our technology into customer workflows .
Note on collaboration and roles: You'll work alongside a Deal Owner , who leads the commercial relationship , and a Customer Success Manager , responsible for post-sale client engagement and support.
This setup allows you to focus on implementation, delivery, execution, and providing clinical, technical and regulatory advisory to the customer — without managing the client relationship end-to-end.
Your responsibilities will center on translating clinical and business needs into clear project plans and specifications , ensuring successful execution across all phases.
While deep technical expertise is not required, a solid foundational understanding of data and technical concepts —such as database structures, data transfer specifications, integrations, and system requirements—is essential to effectively coordinate with technical teams and support seamless projects from definition to the delivery.
You will also provide clinical, technical, and regulatory guidance to customers —without being responsible for managing the full client relationship lifecycle.
What you need to achieve Project planning and execution: Develop and track detailed project plans, manage changes to project scope, schedule, ensuring successful project execution within time, and scope constraints.
Daily customer interaction: Collaborate with customers, investigators, CROs, and Sponsors to ensure project success Team liaison: Act as the crucial link between the commercial team and the product team, facilitating effective communication and ensuring customer needs translate into clear and achievable technical specifications.
Technical and regulatory customer advisory: Provide expert support to help customers generate and understand the best use case for our software medical device, including explaining technical aspects related to product, as well as regulatory feasibility and data protection issues.
Functional and Technical requirements analysis: Thoroughly assess project needs and specifications to ensure alignment with product objectives and customer expectations.
Holistic view of healthcare processes: Offer a comprehensive perspective of healthcare processes to help and support the team in developing effective solutions.
Development specifications and Product documentation Definition: Clearly establish development requirements and ensure the creation of accurate and complete product documentation.
Product strategy participation: Actively contribute to the definition and adjustment of product strategy, ensuring its relevance and success in the market.
Must have Strong knowledge of Good Clinical Practice (GCP) and clinical research regulations Proven experience in project management, especially in the development of software medical devices within the health, biotechnology, or digital health sectors ( hospitals, CROs, Sponsors, research institutions) .
Specific knowledge of AI technologies applied to health and previous experience in dermatology or related fields.
Understanding of medical device regulation, including familiarity with software medical device regulatory frameworks and compliance.
Basic knowledge of data protection laws, such as GDPR and HIPAA compliance, to ensure our products meet the necessary data privacy and security standards.
Deep understanding of the health industry, including B2B dynamics and specific regulations for software medical devices.
Exceptional communication skills, capable of effectively interacting with technical teams, healthcare professionals, and business stakeholders, explaining complex concepts in a clear and accessible manner.
Effective leadership, with experience leading multifunctional teams in dynamic and demanding environments.
Degree in Business Administration, Health Management, Biotechnology or a related field.
Project management certification (e.g., PMP, PRINCE2) is highly valued.
Nice to have Experience with data transfer specifications, database structures, and system integrations in the context of clinical or research studies.
Familiarity with clinical data management systems (CDMS) , electronic data capture (EDC) platforms, and clinical trial software (e.g., Medidata, REDCap, OpenClinica).
Knowledge of healthcare processes and management systems, such as HIS/EHR/EMR, RIS, LIS, PACS, or ERP, as well as standards like FHIR and HL7v2.
Foundational programming knowledge in programming languages such as PHP, JavaScript, or Python.
Important Able to work autonomously, with discipline and with high motivation and energy Proactive, willing to learn, have an impact and grow in the company Team player capable of adapting to changes in a fast-paced environment What do we offer ? Full-remote position.
We are a team of committed professionals, so you choose where you work from and also means that all processes need to be thought of as if we had no office and everyone is working remotely.
No one will feel like an outsider, since all conversation will need to happen on slack or hangouts.
Working in a fast growing Start-up environment within an international context Flexible compensation: daycare and restaurant Flexible vacation policy: 23 working days per year + 2 additional days granted by the company (your birthday and December 7th) + 2 days for company closure per labor agreement (December 24th and 31st) Flexible working hours Full time contract Starting day: as soon as possible.
Competitive salary according to your experience Languages High Spanish and English proficiency (writing and speaking).
Additional languages are a plus In compliance with the provisions of the data protection regulations, we inform you that the personal data you have provided with your resume will be processed in a mixed manner (automated or not) by AI Labs Group, S.L., with NIF B******** and address in Gran Vía, 1, BAT Tower, Bilbao (Bizkaia), ***** (hereinafter, Legit.Health).
The purpose of this data processing is the management of Legit.Health's personnel selection processes and is based on your prior consent.
Your data will be kept for one year, after which we will proceed to cancel it.
You are also informed that no automated decisions will be made.
Your data will not be transferred to third parties.
At any time you can exercise your rights of access, rectification, deletion, portability, limitation, or opposition, by writing to the email ******.
We also inform you that you can go to the Control Authority to assert your data protection rights.
- Please note that this is not an email to submit job applications.
If you wish to apply for a position, please follow the instructions on our official job postings.
Sincerely, Legit.Health team.
Let's Health
Clinical / Medical Director
Let's Health · Valladolid, ES
Teletreball .
We're looking for a Medical Affairs Director!
Are you passionate about shaping global Medical Affairs strategy and driving scientific excellence in healthcare?
At Let's Health, we're growing and looking for aMedical Affairs Directorto lead high-impact strategic initiatives with global biopharma clients.
This role combines scientific leadership, client partnership, and innovation, positioning you as a key member of our leadership team, reporting directly to our CEO.
______________________________________________________________________________
About Let's Health
We only do one thing: help life sciences companies launch and grow their brands.
That takes medical strategy, creative excellence, and sharp technological execution working as one.
We don't collaborate.
We partner.
For 18+ years, we've partnered with the world's leading biopharma companies to turn complex evidence into strategy, content, and campaigns that actually land with HCPs, patients, and decision-makers.
We work across 25+ markets, with 150+ biopharma clients who keep coming back.
And right now, we're in a real growth moment, building the team and the infrastructure to take things to the next level.
If you want to do meaningful work in healthcare, in a place small enough that your contributions genuinely matter, this might be exactly what you're looking for.
______________________________________________________________________________
Your Mission
You will act as thesenior scientific partnerfor our key clients, leading Medical Affairs strategy across the full product lifecycle.
You will translate complex science into actionable strategies, guide global engagements, and strengthen Let's Health's position as a trusted scientific and strategic advisor.
You will also play a critical role inbusiness growth, and innovationworking closely with the CEO and cross-functional teams to evolve our Medical Affairs offering.
______________________________________________________________________________
Key Responsibilities
- Medical Affairs Strategy Design & Planning
Develop structured strategic frameworks and playbooks translating scientific and business priorities into execution.
Act as a strategic advisor to senior stakeholders, ensuring cross-functional alignment.
- Insight Generation & Strategic Integration
Translate insights into clear strategic recommendations directly informing brand and medical decision-making.
- Evidence Translation & Field Enablement
Enable in-field and global teams to deliver consistent, high-impact scientific engagement, bridging the gap between data and execution.
Ensure compliance with global regulatory standards (EFPIA and equivalents).
- KOL Engagement & External Scientific Leadership
Represent Let's Health externally as senior scientific leader and trusted partner.
- Congress & Scientific Events Strategy
Ensure effective post-event insight capture, competitive intelligence, and dissemination to maximize strategic impact.
- Scientific Education, Communication & Content Excellence
Ensure clarity, consistency, and compliance, while driving innovation in scientific communication.
- Training & Capability Building
Equip teams with the knowledge, tools, and capabilities required to execute effectively and engage stakeholders with confidence.
______________________________________________________________________________
What You Bring
Advanced degree in Medicine, Pharmacy, Life Sciences, or related field (PhD/MD preferred).
Extensive experience in Medical Affairs within pharma, MedTech, or healthcare consulting.
Proven track record managing senior client relationships at global level.
Strong strategic thinking and ability to translate science into business impact.
Experience leading multidisciplinary teams and complex international projects.
Deep understanding of regulatory frameworks and compliance standards.
Fluency in English (and ideally also Spanish[GN1] ) with excellent communication and presentation skills
______________________________________________________________________________
What We Offer
A leadership role with high strategic impact in a fast-growing international company.
Collaboration with leading global pharmaceutical companies.
The opportunity to shape the future of Medical Affairs and Let's Health.
A dynamic, innovation-driven, and collaborative work environment in Madrid with up to two remote working days per week.
A culture built on trust, scientific excellence, and continuous development.
A competitive package that values what you bring to the table.
Want to know more?
Send your CV ******.
Let's Health
Clinical / Medical Director
Let's Health · Madrid, ES
Teletreball .
We're looking for a Medical Affairs Director!
Are you passionate about shaping global Medical Affairs strategy and driving scientific excellence in healthcare?
At Let's Health, we're growing and looking for aMedical Affairs Directorto lead high-impact strategic initiatives with global biopharma clients.
This role combines scientific leadership, client partnership, and innovation, positioning you as a key member of our leadership team, reporting directly to our CEO.
______________________________________________________________________________
About Let's Health
We only do one thing: help life sciences companies launch and grow their brands.
That takes medical strategy, creative excellence, and sharp technological execution working as one.
We don't collaborate.
We partner.
For 18+ years, we've partnered with the world's leading biopharma companies to turn complex evidence into strategy, content, and campaigns that actually land with HCPs, patients, and decision-makers.
We work across 25+ markets, with 150+ biopharma clients who keep coming back.
And right now, we're in a real growth moment, building the team and the infrastructure to take things to the next level.
If you want to do meaningful work in healthcare, in a place small enough that your contributions genuinely matter, this might be exactly what you're looking for.
______________________________________________________________________________
Your Mission
You will act as thesenior scientific partnerfor our key clients, leading Medical Affairs strategy across the full product lifecycle.
You will translate complex science into actionable strategies, guide global engagements, and strengthen Let's Health's position as a trusted scientific and strategic advisor.
You will also play a critical role inbusiness growth, and innovationworking closely with the CEO and cross-functional teams to evolve our Medical Affairs offering.
______________________________________________________________________________
Key Responsibilities
- Medical Affairs Strategy Design & Planning
Develop structured strategic frameworks and playbooks translating scientific and business priorities into execution.
Act as a strategic advisor to senior stakeholders, ensuring cross-functional alignment.
- Insight Generation & Strategic Integration
Translate insights into clear strategic recommendations directly informing brand and medical decision-making.
- Evidence Translation & Field Enablement
Enable in-field and global teams to deliver consistent, high-impact scientific engagement, bridging the gap between data and execution.
Ensure compliance with global regulatory standards (EFPIA and equivalents).
- KOL Engagement & External Scientific Leadership
Represent Let's Health externally as senior scientific leader and trusted partner.
- Congress & Scientific Events Strategy
Ensure effective post-event insight capture, competitive intelligence, and dissemination to maximize strategic impact.
- Scientific Education, Communication & Content Excellence
Ensure clarity, consistency, and compliance, while driving innovation in scientific communication.
- Training & Capability Building
Equip teams with the knowledge, tools, and capabilities required to execute effectively and engage stakeholders with confidence.
______________________________________________________________________________
What You Bring
Advanced degree in Medicine, Pharmacy, Life Sciences, or related field (PhD/MD preferred).
Extensive experience in Medical Affairs within pharma, MedTech, or healthcare consulting.
Proven track record managing senior client relationships at global level.
Strong strategic thinking and ability to translate science into business impact.
Experience leading multidisciplinary teams and complex international projects.
Deep understanding of regulatory frameworks and compliance standards.
Fluency in English (and ideally also Spanish[GN1] ) with excellent communication and presentation skills
______________________________________________________________________________
What We Offer
A leadership role with high strategic impact in a fast-growing international company.
Collaboration with leading global pharmaceutical companies.
The opportunity to shape the future of Medical Affairs and Let's Health.
A dynamic, innovation-driven, and collaborative work environment in Madrid with up to two remote working days per week.
A culture built on trust, scientific excellence, and continuous development.
A competitive package that values what you bring to the table.
Want to know more?
Send your CV ******.
Clinica El
Mijas, ES
RECEPCIONISTA - AUX CONTABLE/ADMINISTRATIVO
Clinica El · Mijas, ES
.
Somos un centro médico privado que se encuentra ubicado en Sitio de Calahonda-Mijas Costa-Málaga y buscamos incorporar de forma estable personal que se encargue de tareas de atención al cliente y administrativas.
Tasks
Buscamos incorporar a nuestro equipo un profesional que de atención al cliente y lleve la gestión administrativa de la documentación generada en nuestro centro médico.
Horario: Lunes a Viernes 09.00 h a 19.00 h y sábados de 10.00 h a 14.00 h (alternando con otra compañera un máximo de 40h semanales)
Requirements
- Dominio de los idiomas inglés y español, tanto hablado como escrito. Valorable otros idiomas.
- Sólidas habilidades organizativas y multitarea, con atención al detalle.
- Familiarización con software de contabilidad y tareas administrativas generales.
- Excelentes habilidades interpersonales y de comunicación para la interacción con pacientes.
- Capacidad para trabajar eficazmente en equipos pequeños y adaptarse a diversos roles.
Benefits
Estabilidad profesional
Salario 1200 netos al mes
Queremos a una persona que quiera formar parte de un gran equipo de profesionales, comprometido y empático. En nuestro centro médico somos una gran familia y eso queremos transmitir a nuestros pacientes también. Atender al público no siempre es fácil y menos en el entorno sanitario por lo que la persona que aplique al puesto debe tener el perfil requerido.
Principal Clinical Scientist
19 d’abr.Alignerr
Principal Clinical Scientist
Alignerr · Madrid, ES
Teletreball .
Principal Clinical Scientist (AI Training)
About The Role
What if your career-long expertise in clinical trial design and regulatory science could directly influence how AI understands and reasons about clinical evidence? We're looking for a Principal Clinical Scientist to bring senior-level rigor to AI-driven research — ensuring the clinical data powering next-generation AI systems meets the standards expected in real-world regulatory submissions.
This is a fully remote, flexible contract role designed for experienced clinical scientists who want to work at the frontier of AI and biomedical research. No AI background required — just deep clinical expertise and a sharp eye for scientific quality.
- Organization: Alignerr
- Type: Hourly Contract
- Location: Remote
- Commitment: 10–40 hours/week
- Design and review clinical trial protocols used to generate high-quality, regulatory-grade datasets for AI training and evaluation
- Interpret and audit clinical trial results to ensure accuracy, consistency, and alignment with regulatory standards
- Evaluate AI-generated clinical analyses for scientific soundness and regulatory relevance
- Provide expert, structured feedback that helps AI models reason more accurately about clinical trial data, outcomes, and methodology
- Work independently and asynchronously — fully on your own schedule
- Senior-level experience designing clinical trial protocols for regulatory submission (FDA, EMA, or equivalent)
- Deep expertise interpreting clinical data within regulatory frameworks
- Strong foundation in clinical research methodology, biostatistics, or translational science
- Naturally detail-oriented with high standards for scientific accuracy and consistency
- Clear and effective written communicator able to document feedback in structured formats
- Prior experience with data annotation, data quality review, or AI evaluation workflows
- Background in pharmacology, epidemiology, or outcomes research
- Familiarity with AI tools or clinical decision-support systems
- Experience working across multiple therapeutic areas or trial phases
- Work directly on frontier AI systems shaping the future of clinical and biomedical research
- Influence how AI understands, evaluates, and reasons about real-world clinical evidence
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with the structure of meaningful, expert-level work
- Collaborate with leading AI research labs and teams pushing the boundaries of medical AI
- Potential for ongoing work and contract extension as new projects launch