What remote healthcare jobs are available?

Remote healthcare roles include medical coder ($48,000-$72,000), medical biller ($40,000-$55,000), telehealth nurse ($68,000-$95,000), utilization review nurse ($75,000-$100,000), case manager ($72,000-$95,000), clinical research coordinator ($58,000-$80,000), and health informatics specialist ($80,000-$120,000). Administrative and IT roles offer the most remote opportunities. Clinical roles require state licensure in patient locations.

How much do remote medical coders make?

Remote medical coders earn $48,000-$75,000 depending on certification and specialty. Entry-level coders start at $42,000-$52,000. CPC or CCS certified coders earn $52,000-$68,000. Risk adjustment and surgical coding specialists command $65,000-$85,000. Remote coding positions outnumber office positions 3:1. Productivity bonuses add $5,000-$12,000 annually for coders exceeding accuracy and volume targets.

Can nurses work from home?

Registered nurses work remotely in telehealth triage ($68,000-$90,000), utilization review ($75,000-$100,000), case management ($72,000-$95,000), clinical documentation improvement ($70,000-$92,000), and nurse education ($68,000-$88,000). Active RN license required; multistate compact licenses enable working with patients across 40+ states. Telehealth nursing grew 400% since 2020 and continues expanding as healthcare systems adopt virtual care models.

What certifications do remote healthcare jobs require?

Medical coding requires CPC (AAPC) or CCS (AHIMA) certification—90% of remote coding jobs require certification. Nursing roles require active RN license plus specialty certifications: CCM for case management, CPUM for utilization review. Health information management requires RHIA or RHIT. HIPAA compliance training is mandatory for all remote healthcare positions. Most certifications require 3-12 months preparation and passing standardized exams.

How do remote healthcare workers maintain HIPAA compliance?

HIPAA compliance requires encrypted VPN connections, HIPAA-compliant video platforms (Zoom Healthcare, Doxy.me), private workspaces where family cannot see screens, and employer-provided secure equipment. Protected health information (PHI) cannot be stored on personal devices. Employers provide annual compliance training and conduct security audits. HIPAA violations carry penalties from $100 to $50,000 per incident, with criminal charges for willful neglect.

How do I become a medical coder working from home?

Complete a medical coding certificate program (4-6 months, $2,000-$4,000) covering ICD-10, CPT, and HCPCS coding systems. Pass CPC or CCS certification exam (70% pass rate with preparation). Entry-level coders work in-office for 6-12 months before transitioning to remote, though some employers hire directly into remote positions. Certified coders find employment within 3 months—job placement rates exceed 85% for accredited program graduates.

What is telehealth nursing?

Telehealth nurses assess patients via phone and video, providing triage recommendations, chronic disease monitoring, post-discharge follow-up, and health education. RN license and 2+ years clinical experience required. Telehealth nurses earn $68,000-$95,000, comparable to bedside nursing without physical demands or exposure risks. Shifts cover 8-12 hours with flexible scheduling options. Major employers include UnitedHealth, CVS Health, and Teladoc.

What is the future of remote healthcare jobs?

Remote healthcare employment is projected to grow 28% by 2030, outpacing overall healthcare growth of 13%. Telehealth visits now represent 20% of all outpatient care, up from 1% in 2019. Medical coding, telehealth, and health informatics show strongest remote growth trajectories. AI will augment rather than replace remote healthcare roles—human oversight remains essential for clinical decision-making and patient communication.

Remote Healthcare Jobs in Poland (74)

Senior Clinical Research Associate, Sponsor dedicated in Poland

IQVIA · Full Time · Yesterday

IQVIA

🌎 Poland 💵 171K - 375K per year ⭐ 2-5 yrs exp 💼 Healthcare

The Senior CRA is responsible for performing site selection, initiation, monitoring, and close-out visits while ensuring compliance with GCP and ICH guidelines. They also manage study progress by tracking regulatory submissions, recruitment, and data integrity.

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Medical Director - Oncology , Sponsor Dedicated (Home-Based)

IQVIA · Full Time · 2 Days Ago

IQVIA

🌎 Poland 💵 314K - 667K per year ⭐ 10+ yrs exp 💼 Healthcare Medical Director

The Medical Director provides medical and scientific oversight for clinical research programs, serving as the primary medical monitor for sponsor companies. Responsibilities include protocol development, safety monitoring, SAE reporting, and providing medical expertise to project teams throughout the clinical trial lifecycle.

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Principal Biostatistician

Fortrea · Full Time · 2 Days Ago

Fortrea

🌎 Bulgaria, Greece, Hungary, Oman, Poland, Romania, Slovakia, United Kingdom ⭐ 10+ yrs exp 💼 Healthcare

Lead statistical strategy and delivery for complex clinical trials, ensuring high-quality outputs and regulatory compliance. Provide technical leadership, mentor junior staff, and collaborate with multidisciplinary stakeholders to support global programs.

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Senior CTM - Internal Medicine (Dermatology, Cardiovascular, Liver, Nephrology, Immunology, Rare Disease, Diabetes)

Thermo Fisher Scientific · Full Time · 2 Days Ago

Thermo Fisher Scientific

🌎 Bulgaria, France, Greece, Italy, Oman, Poland, Romania, Serbia, Spain, United Kingdom ⭐ 5-10 yrs exp 💼 Healthcare

The Senior Clinical Team Manager directs and coordinates the technical and operational aspects of clinical trials to ensure successful completion within budget and timelines. They manage clinical and start-up activities, lead project teams, and maintain compliance with ICH GCP and regulatory standards.

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Clinical Research Associate II

Emmes Group · Full Time · 3 Days Ago

Emmes Group

🌎 Poland ⭐ 2-5 yrs exp 💼 Healthcare

The Clinical Research Associate II monitors clinical study sites to ensure trials are conducted in accordance with protocols, SOPs, and regulatory requirements. They perform site visits, verify source data, manage site documentation, and provide training to site staff under minimal supervision.

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Freelance Clinical Research Associate

TFS HealthScience · Freelance · 3 Days Ago

TFS HealthScience

🌎 Poland, United States ⭐ 2-5 yrs exp 💼 Healthcare

The Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with regulatory requirements and SOPs. They ensure subject safety and data integrity by reviewing source documentation and managing investigational products.

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Clinical Rater (Poland)

Brooklyn Health · Freelance · 3 Days Ago

Brooklyn Health

🌎 Poland 💵 $150 - $350 per hour ⭐ 5-10 yrs exp 💼 Healthcare

Perform manual, independent reviews of clinical trial interviews and scale administrations to ensure scoring accuracy and protocol adherence. Senior roles will also oversee site performance, interpret rater patterns, and manage targeted site interventions.

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Clinical Research Manager

TFS HealthScience · Full Time · 3 Days Ago

TFS HealthScience

🌎 Poland, Spain 💵 €63000 - €65000 per year ⭐ 5-10 yrs exp 💼 Healthcare

The Clinical Research Manager oversees clinical trial operations, ensuring compliance with study protocols, SOPs, and ICH-GCP guidelines. They lead study teams, manage site performance, and serve as the primary point of contact for sponsors and investigative sites.

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Freelance Senior Clinical Research Associate

TFS HealthScience · Freelance · 4 Days Ago

TFS HealthScience

🌎 Poland ⭐ 5-10 yrs exp 💼 Healthcare

The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with SOPs and regulatory requirements. They will collaborate with study teams and investigative sites to ensure data integrity, subject safety, and timely execution of study deliverables.

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Vice President, Medical Affairs (Psychiatry)

Premier Research · Full Time · 4 Days Ago

Premier Research

🌎 Belgium, Bulgaria, Ireland, Netherlands, Oman, Poland, Romania, Spain, United Kingdom ⭐ 10+ yrs exp 💼 Healthcare

Serve as the primary medical and scientific strategic lead for psychiatry-focused clinical studies and business development. Collaborate with cross-functional teams to design protocols, execute study strategies, and provide expert medical input for internal and external stakeholders.

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Clinical Trial Supply Manager

ICON plc · Full Time · 4 Days Ago

ICON plc

🌎 Bulgaria, Poland, Spain ⭐ 5-10 yrs exp 💼 Healthcare

Oversee the planning and execution of clinical supplies projects to ensure regulatory compliance and timely delivery. Collaborate with cross-functional teams to manage project timelines, budgets, and logistics while addressing potential risks.

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Clinical Trial Psych Rater - Hungarian Speaking

IQVIA · Part Time · 5 Days Ago

IQVIA

🌎 Austria, Bosnia and Herzegovina, Bulgaria, Croatia, Hungary, Latvia, Lithuania, Poland, Serbia, Slovakia, Switzerland, United States ⭐ 2-5 yrs exp 💼 Healthcare

The Clinical Specialist reviews clinical trial data and assessment scales to ensure standardized practices and data integrity. They also provide guidance to raters through live interactions, feedback, and functional assessments.

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Associate Director, Clinical Trial Manager RWLP Homebased POLAND

Syneos Health · Full Time · 5 Days Ago

Syneos Health

🌎 Poland ⭐ 10+ yrs exp 💼 Healthcare

Provide leadership to clinical operations within the APAC region to ensure the overall delivery and performance of clinical trials. Collaborate with cross-functional teams to navigate drug development complexities and meet customer goals.

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Director, Medical Affairs, Poland

Revolution Medicines · Full Time · 6 Days Ago

Revolution Medicines

🌎 Poland ⭐ 10+ yrs exp 💼 Healthcare

The Director of Medical Affairs for Poland is responsible for defining and executing the local medical strategy for the oncology portfolio. This role involves leading scientific exchange, building relationships with key opinion leaders, and ensuring alignment between global strategy and local healthcare needs.

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Senior Clinical Data Manager

Everest Clinical Research · Full Time · 6 Days Ago

Everest Clinical Research

🌎 Poland, United States ⭐ 5-10 yrs exp 💼 Healthcare

The Senior Clinical Data Manager leads data management activities, including project planning, database design, and ensuring high-quality deliverables for clinical trials. They act as the primary contact for clients, manage timelines, and provide training and oversight to the data management team.

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Manager, Global Clinical Monitoring

Precision Medicine Group · Full Time · 6 Days Ago

Precision Medicine Group

🌎 Poland ⭐ 5-10 yrs exp 💼 Healthcare

The Manager, Global Clinical Monitoring is responsible for the line management, performance, and development of CRAs, IHCRAs, and CTMs within an assigned European region. They also contribute to operational excellence initiatives, process improvements, and strategic resource allocation to ensure high-quality clinical trial execution.

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Manager, Global Clinical Monitoring

Precision for Medicine · Full Time · 6 Days Ago

Precision for Medicine

🌎 Poland ⭐ 5-10 yrs exp 💼 Healthcare

The Manager, Global Clinical Monitoring is responsible for the line management, performance, and development of CRAs, IHCRAs, and CTMs across Europe. They also contribute to operational excellence initiatives and ensure high-quality execution of clinical operations activities.

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Clinical Lead / Clinical Trial Manager (Europe) - Talent Pipeline Opportunity

Emerald Clinical Trials · Full Time · 6 Days Ago

Emerald Clinical Trials

🌎 Albania, Andorra, Belgium, Bulgaria, Croatia, Denmark, Estonia, Finland, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Malta, Netherlands, Norway, Oman, Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, United Kingdom ⭐ 5-10 yrs exp 💼 Healthcare

Lead day-to-day clinical trial operations from start-up through close-out while managing study timelines and enrolment targets. Provide oversight of CRA activities, ensure protocol compliance, and manage relationships with sponsors and investigators.

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Clinical Research Associate - Talent Pipeline Opportunity

Emerald Clinical Trials · Full Time · 6 Days Ago

Emerald Clinical Trials

The Clinical Research Associate is responsible for conducting site visits, ensuring protocol compliance, and maintaining high-quality study documentation. They will also manage site relationships, support patient recruitment, and validate study data throughout the clinical trial lifecycle.

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Clinical Project Leader / Senior Project Leader - Biotech (Select EU countries)

Parexel · Full Time · 1 Week Ago

Parexel

🌎 Croatia, Hungary, Ireland, Lithuania, Oman, Poland, Romania, Spain, United Kingdom ⭐ 5-10 yrs exp 💼 Healthcare

The Clinical Project Leader will provide cross-functional leadership for clinical trials, ensuring projects are delivered on time, within budget, and in compliance with ICH GCP standards. They are responsible for managing client relationships, project P&L, and mitigating risks throughout the project lifecycle.

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Clinical Research Associate - Poznan - FSP

Parexel · Full Time · 1 Week Ago

Parexel

🌎 Poland 💵 220K - 240K per year ⭐ 2-5 yrs exp 💼 Healthcare

You will be responsible for all site management and supervisory activities for oncology studies while working with industry leaders. Additionally, you will mentor junior CRAs and ensure compliance with clinical research guidelines.

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Senior Manager Physician Partnership

Johnson & Johnson Innovative Medicine · Full Time · 1 Week Ago

Johnson & Johnson Innovative Medicine

🌎 Austria, Belgium, Bulgaria, Croatia, Denmark, Estonia, France, Germany, Hungary, Italy, Latvia, Lithuania, Netherlands, Poland, Serbia, Slovakia, Slovenia, Spain, Sweden 💵 €96000 - €165K per year ⭐ 10+ yrs exp 💼 Healthcare

The Senior Manager will foster and maintain strategic relationships with electrophysiologists and key accounts across the EMEA region. They will act as a liaison between the organization and stakeholders to ensure consistent service, strategic engagement, and effective collaboration.

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Investigator Payments Lead - Senior Associate / Clinical Site Payments Lead - Senior Associate - Poland (Home-based) - FSP

Parexel · Full Time · 1 Week Ago

Parexel

🌎 Poland ⭐ 2-5 yrs exp 💼 Healthcare

Manage the full lifecycle of clinical site payment administration, including protocol schedules, budget configurations, and payment triggers. Troubleshoot payment failures and provide oversight of vendors to ensure adherence to contractual terms and operational standards.

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Regional Medical Science Liaison (MSL) - Breast Cancer / Oncology - Poland/Czech Rep

Amplity Health · Full Time · 1 Week Ago

Amplity Health

🌎 Poland ⭐ 5-10 yrs exp 💼 Healthcare

The Regional Medical Science Liaison will serve as a scientific partner to healthcare professionals and investigators to support clinical development and medical affairs activities. They will facilitate scientific education, manage KOL relationships, and provide field-based insights to shape medical strategy.

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Senior Clinical Research Associate - Oncology, Hematology, CNS - Poland

Worldwide Clinical Trials · Full Time · 1 Week Ago

Worldwide Clinical Trials

🌎 Poland ⭐ 2-5 yrs exp 💼 Healthcare

The Senior CRA is responsible for site qualification, initiation, monitoring, and close-out visits to ensure protocol adherence and data integrity. They also provide mentorship to less experienced staff and ensure compliance with regulatory and trial master file documentation.

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Clinical Auditing Specialist II/III - Vendor and Information System Audits Team

Thermo Fisher Scientific · Full Time · 1 Week Ago

Thermo Fisher Scientific

🌎 Belgium, Bulgaria, Hungary, Poland, Serbia, United Kingdom ⭐ 5-10 yrs exp 💼 Healthcare

Conduct and lead external supplier GxP information systems audits for clinical trials while providing regulatory consultation to internal teams. Prepare detailed audit reports and contribute to practical process improvement efforts across the organization.

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Medical Services Specialist with Czech and English Language (100% Remote)

Conduent Poland Sp. z o.o. · Other, Full Time · 1 Week Ago

Conduent Poland Sp. z o.o.

🌎 Poland 💵 €1.5 per day ⭐ 2-5 yrs exp 💼 Healthcare

Manage customer inquiries regarding products and disease states while providing world-class service via phone, email, and written communication. Maintain accurate records of interactions and ensure compliance with industry regulations and adverse event reporting processes.

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Medical Services Specialist with Czech and English Language (100% Remote)

Conduent · Full Time · 1 Week Ago

Conduent

🌎 Poland ⭐ 2-5 yrs exp 💼 Healthcare

Manage customer inquiries regarding products and disease states via telephone, email, and written communication. Provide accurate medical information while maintaining compliance with industry regulations and internal quality processes.

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Regional Clinical Study Manager

BeiGene · Full Time · 1 Week Ago

BeiGene

🌎 Poland 💵 281K - 352K per year ⭐ 5-10 yrs exp 💼 Healthcare

The Regional Clinical Study Manager is accountable for regional study delivery, ensuring quality, inspection readiness, and adherence to timelines and budgets. They lead the regional clinical operations team, manage external vendors, and act as the primary point of escalation for study-related issues.

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Senior Clinical Study & Line Manager

BeiGene · Full Time · 1 Week Ago

BeiGene

🌎 Poland 💵 325K - 406K per year ⭐ 5-10 yrs exp 💼 Healthcare

The role involves line managing clinical study managers, overseeing their performance, and ensuring clinical trials are executed according to ICH/GCP guidelines and corporate standards. The manager will also drive process improvements, allocate resources, and provide local expertise to support clinical trial activities.