Remote Healthcare Jobs in Spain
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Provide medical leadership to study teams by creating protocols, ensuring subject safety, and performing real-time medical monitoring. Collaborate with cross-functional teams to interpret clinical data and ensure compliance with regulatory standards and SOPs.
The Medical Director provides medical leadership and support for clinical trials, including protocol creation, site selection, and real-time medical monitoring. They serve as the primary medical point of contact for internal and external stakeholders, ensuring study compliance and safety throughout all phases.
The Medical Director provides medical oversight for clinical studies, acting as a Medical Monitor to ensure subject safety and data integrity. They also provide therapeutic input for protocol development, study start-up, and regulatory compliance.
Translate, post-edit, and review clinical trial documentation to ensure adherence to medical and ethical standards. Collaborate with teams to enhance the readability and accuracy of scientific materials while maintaining regulatory compliance.
The VP of Medical Science and Strategy will lead the development and execution of medical strategies for cardiovascular programs. This role involves cross-functional leadership to ensure scientific excellence and alignment with clinical development goals.
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The Medical Science Liaison cultivates strategic partnerships with Key Opinion Leaders and executes medical strategy for the Hematology portfolio. This role involves delivering scientific support, gathering expert insights, and facilitating internal training to ensure high standards of therapeutic expertise.
The consultant will assess client revenue cycle operations, medical records practices, and EMR workflows to identify gaps and compliance risks. They are also responsible for configuring EMR forms, templates, and billing procedures to ensure regulatory compliance and operational efficiency.
The Care Coordinator manages a panel of patients in CCM and RPM programs, conducting outreach and providing health education. They are responsible for monitoring patient data, updating care plans, and ensuring seamless communication between patients and healthcare providers.
Develop and maintain comprehensive clinical study timelines from protocol concept through database lock while ensuring alignment with asset-level plans. Coordinate across stakeholders to manage risks, dependencies, and resource planning while driving operational excellence and milestone achievement.
You will coordinate and manage the day-to-day operational activities of clinical trials, including participant recruitment and site logistics. Additionally, you will ensure strict adherence to study protocols, regulatory requirements, and Good Clinical Practice standards.
The Study Management Associate III provides strategic leadership and oversight for global clinical trials, managing cross-functional teams and external vendors from inception through closure. They are responsible for ensuring inspection readiness, managing study budgets and timelines, and overseeing critical systems like EDC, IRT, and eTMF.
The Clinical Trial Liaison acts as a field-based scientific expert to accelerate clinical trial execution by building relationships with investigators and site staff. They are responsible for driving site engagement, addressing enrollment barriers, and communicating clinical insights to internal study teams.
The Clinical Trials Associate provides essential administrative and project tracking support to ensure clinical trials remain organized and on schedule. Responsibilities include maintaining project documentation, managing system access, and coordinating site information across global teams.
The Clinical Research Associate II is responsible for conducting monitoring visits, ensuring data integrity, and maintaining trial documentation in compliance with ICH/GCP guidelines. They will manage site activities, prepare monitoring reports, and ensure patient safety throughout the clinical study process.
The Proposals and Contracts Manager is responsible for leading the end-to-end RFP process and managing contract negotiations across various accounts. They will collaborate with internal stakeholders and clients to ensure proposals and contracts align with operational standards and project requirements.
The Director serves as a strategic business partner and Chief of Staff to the Head of Global Clinical Development Operations, driving operational cadence and strategic alignment. They are responsible for multi-year workforce planning, financial budget management, and leading functional integration for business development activities.
Provide non-clinical support to patients and other stakeholders through inbound and outbound calls, email, chat, and text, including connecting patients with resources and referring them to clinical support when appropriate. Maintain accurate, compliant documentation, manage multiple requests and follow-ups, and collaborate with clinical educator teams to improve patient satisfaction and service delivery.
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The Senior Clinical Trial Manager oversees clinical trial operations, including budget management, study oversight, and the development of monitoring plans. They are also responsible for mentoring Clinical Research Associates, driving study start-up and enrollment, and fostering productive relationships with sponsors and vendors.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Additionally, you will conduct site visits, resolve issues, and collaborate with cross-functional teams to ensure accurate data collection and reporting.
The Senior Clinical Research Associate II is responsible for site monitoring, site management, and ensuring adherence to regulatory guidelines and project plans. They act as a lead monitor for clinical studies, manage study files, and oversee data integrity through source document review.
You will deliver remote medical consultations to Polish-speaking patients as part of a global digital healthcare team. The role involves integrating into existing operations while maintaining flexibility in your working schedule.
Implement and configure billing applications and related software solutions to meet client requirements, applying revenue cycle management expertise and best practices. Coordinate with clients, development, and engineering teams on testing, troubleshooting, project plans, risk mitigation, documentation, training, and end-user support.
The Clinical Lead II oversees clinical and site start-up strategies, ensuring study budgets and timelines are met while managing risks. They collaborate with cross-functional teams to drive patient recruitment and represent the clinical function in sponsor communications.
The Senior Clinical Data Coordinator will lead clinical coding activities, manage third-party data, and act as the lead Data Manager for assigned studies. They are responsible for producing and validating eCRFs and databases while ensuring adherence to project timelines and quality standards.
The Clinical Trial Liaison will build relationships with investigators and site teams to provide scientific guidance and support trial delivery. They are responsible for optimizing patient recruitment strategies and ensuring study teams understand protocol requirements and enrolment goals.
The Clinical Trial Manager will oversee clinical development projects to ensure the efficient delivery of therapies while maintaining high standards of quality. They will collaborate with cross-functional teams to streamline processes and achieve customer goals within a global environment.
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The Senior Clinical Research Associate manages the full site monitoring lifecycle, ensuring compliance with GCP, protocols, and regulatory requirements. They also act as a Lead CRA to coordinate global studies, mentor junior staff, and partner with project teams to ensure study milestones are met.
Translate, post-edit, and review clinical trial documentation to ensure adherence to medical and ethical standards. Collaborate with teams to enhance the readability and accuracy of scientific materials while maintaining regulatory compliance.
The Senior Director will provide executive leadership and strategic oversight for pharmacy operations across the European network, ensuring compliance with regulatory standards. They will lead investigational drug services, drive operational excellence, and mentor pharmacy teams to support organizational growth.
The virtual assistant will provide administrative support specifically for dental and orthodontic practices. Responsibilities include managing patient communications, scheduling, and general office tasks remotely.
Stop the endless job search. Our AI finds and applies to the best jobs for you.
We reviewed 57 job postings for remote healthcare professionals in Spain and found these are the skills employers ask for most often:
| Skill | Share of job posts |
|---|---|
| Project management | 42% |
| Regulatory compliance | 33% |
| Stakeholder management | 25% |
| Problem-solving | 23% |
| Clinical research | 23% |
| Communication | 19% |
| Data analysis | 19% |
| Clinical trial management | 18% |
| Clinical trials | 18% |
| Good Clinical Practice | 16% |
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