Where can I find remote jobs?

DailyRemote, LinkedIn, and We Work Remotely are the top platforms for finding remote jobs in 2026. Company career pages at remote-first organizations like GitLab, Zapier, and Automattic list positions directly. FlexJobs and Remote.co offer curated listings with employer verification. Over 85,000 new remote positions are posted weekly across these platforms combined.

How much do remote jobs pay?

Remote jobs pay $50,000 to $200,000 annually, with software developers averaging $120,000, marketing managers $95,000, product managers $140,000, and customer support roles $45,000. Remote salaries match or exceed office equivalents at 78% of companies. Geographic arbitrage allows remote workers to earn San Francisco salaries ($150,000+) while living in lower-cost regions.

What remote jobs can I get with no experience?

Customer support representative ($35,000-$45,000), virtual assistant ($30,000-$50,000), data entry specialist ($28,000-$40,000), social media coordinator ($40,000-$55,000), and sales development representative ($50,000-$70,000 OTE) hire candidates without prior experience. These five roles account for 60% of entry-level remote job postings and require only communication skills and reliable internet.

What is the difference between remote and hybrid work?

Remote work means 100% work-from-anywhere with no office requirement. Hybrid work requires 2-3 office days weekly and limits where employees can live. 32% of US jobs are fully remote, 27% are hybrid, and 41% are fully in-office. Fully remote workers report 25% higher job satisfaction than hybrid workers. Hybrid roles pay 5-10% less than equivalent fully remote positions.

How do I prepare for a remote job interview?

Test camera, microphone, and internet speed 24 hours before the interview. Position lighting in front of your face, not behind. Use a neutral background or professional virtual background. Close all browser tabs and applications to prevent notifications. Dress professionally from head to toe. Look at your camera when speaking, not the screen. 67% of hiring managers have rejected candidates due to technical issues during video interviews.

What are the best countries for digital nomads?

Portugal ranks #1 for digital nomads with affordable cost of living ($2,000/month in Lisbon), fast internet (average 200 Mbps), Digital Nomad Visa, and strong expat community. Spain, Mexico, Thailand, and Colombia round out the top five. Key factors: time zone overlap with US/EU employers, cost of living under $2,500/month, reliable 50+ Mbps internet, and visa accessibility. Portugal and Spain offer paths to EU residency.

Are work from home jobs legit?

Yes, the majority of work from home jobs are legitimate. In 2026, over 35% of US workers hold fully remote positions at verified companies. To identify legit work from home jobs: check that the company has a real website and LinkedIn presence, never pay upfront fees to apply, verify the company on Glassdoor or Trustpilot, and apply through established job boards like DailyRemote that screen employers. Red flags include requests for personal banking information, guaranteed high income with no experience, and unprofessional communication. Remote-first companies like GitLab, Zapier, Automattic, and Shopify post legitimate work from home positions regularly.

What remote jobs are hiring immediately?

Customer support, data entry, virtual assistant, sales development, and content moderation roles are the remote jobs most commonly hiring immediately. These positions typically have a 1-2 week hiring process compared to 4-6 weeks for technical roles. Companies like Amazon, UnitedHealth Group, and CVS Health regularly post remote jobs with immediate start dates. On DailyRemote, new remote jobs are posted every day across 15+ categories, and many positions accept applications within 24 hours of posting. Filter by "latest" to see the most recently added remote jobs hiring now.

What are the easiest remote jobs to get?

The easiest remote jobs to get are customer service representative ($35,000-$50,000), data entry clerk ($28,000-$42,000), virtual assistant ($30,000-$55,000), transcriptionist ($25,000-$45,000), and online tutor ($30,000-$60,000). These roles require no specialized degree, have high hiring volume, and many offer part-time or flexible schedules. Most need only a computer, reliable internet, and basic communication skills. Customer service alone accounts for 25% of all entry-level remote job postings, and many companies provide paid training for new hires.

Are there part-time remote jobs?

Part-time remote jobs are widely available across multiple industries. Common part-time remote positions include customer support (20-30 hours/week), freelance writing ($25-$75/hour), virtual assistant (15-25 hours/week), online tutoring (10-20 hours/week), and bookkeeping (15-20 hours/week). About 30% of all remote job listings on DailyRemote offer part-time or flexible schedules. Many part-time remote jobs let you set your own hours, making them ideal for parents, students, or anyone building a side income. Companies like Belay, Time Etc, and Fancy Hands specialize in part-time remote positions.

Can I work remotely from anywhere in the world?

Many remote jobs allow you to work from anywhere in the world, though some have location restrictions for tax and legal reasons. Fully distributed companies like GitLab, Automattic, Toptal, and Deel hire in 50+ countries. International remote workers should consider time zone requirements (many US companies require 4+ hours overlap), tax implications in their country, and visa requirements. 54 countries now offer digital nomad visas including Portugal, Spain, Costa Rica, and Thailand. On DailyRemote, filter by "Worldwide" location to find remote jobs with no geographic restrictions.

What are the best work from home jobs?

The best work from home jobs in 2026 by salary and job satisfaction are: software engineer ($120,000-$200,000), product manager ($130,000-$180,000), UX designer ($95,000-$160,000), data analyst ($75,000-$120,000), and digital marketing manager ($80,000-$130,000). For non-technical roles, the best options are project manager ($85,000-$140,000), technical writer ($70,000-$110,000), and account executive ($80,000-$150,000 OTE). The best part-time work from home jobs include freelance writing, bookkeeping, and online tutoring. DailyRemote lists the best remote positions across 15+ categories — use the salary filter to find high-paying work from home jobs in your field.

What are high paying remote jobs?

The highest paying remote jobs are in technology, finance, and healthcare. Software architects earn $180,000-$300,000, engineering managers $170,000-$250,000, product directors $200,000-$350,000, and cybersecurity engineers $150,000-$220,000. In non-tech fields, remote sales directors earn $150,000-$250,000 OTE, management consultants $120,000-$200,000, and medical directors $200,000-$400,000. For entry-level workers seeking high pay without experience, sales development ($50,000-$80,000 OTE) and technical support ($45,000-$65,000) offer the best starting salaries with rapid advancement potential. Browse high-paying remote jobs on DailyRemote using the salary filter.

Remote Clinical Research Jobs (1,568)

Director (Country Head) , Clinical Operations

Parexel · Full Time · 20 mins ago

Parexel

🌎 Czech Republic ⭐ 10+ yrs exp 💼 Healthcare

The Director of Clinical Operations oversees a team of managers and individual contributors to ensure high-quality, timely project delivery within budget. They are responsible for talent development, resource planning, and driving business growth through client engagement and strategic leadership.

clinical-research technical-support communication feedback operations training leadership

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SR CRA

ICON plc · Full Time · 20 mins ago

ICON plc

🌎 Poland ⭐ 5-10 yrs exp 💼 Others

You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Responsibilities include conducting site visits, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data collection.

clinical-research training compliance

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Medical Writer II

ICON plc · Full Time · 20 mins ago

ICON plc

🌎 United Kingdom ⭐ 2-5 yrs exp 💼 Writing Medical Writer

The Medical Writer II is responsible for developing and writing clinical trial documents, regulatory submissions, and scientific publications while ensuring accurate interpretation of clinical data. They also assist in managing medical writing resources and support business development activities through research and proposal writing.

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Regulatory Coordinator

Nemours Children's Health · Full Time · 21 mins ago

Nemours Children's Health

🌎 United States ⭐ 2-5 yrs exp 💼 Legal

The Regulatory Coordinator manages the regulatory lifecycle of pediatric oncology clinical trials, ensuring compliance with federal regulations and institutional policies. They oversee the electronic regulatory binder system, coordinate study start-up activities, and facilitate audit-ready documentation across the enterprise.

clinical-research operations training science documentation compliance

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Site Payments Specialist

ICON plc · Full Time · 1 hour ago

ICON plc

🌎 Bulgaria, Poland, Spain ⭐ 2-5 yrs exp 💼 Others

The Site Payments Specialist is responsible for configuring and maintaining site payment systems and study budgets to ensure accurate financial operations. They will collaborate with study teams and investigative sites to manage payment requirements, resolve discrepancies, and ensure compliance with clinical trial agreements.

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Investigator Payment Lead - Senior Associate

ICON plc · Full Time · 1 hour ago

ICON plc

🌎 Bulgaria, Poland, Spain ⭐ 2-5 yrs exp 💼 Others

The Investigator Payments Lead manages the end-to-end administration of site and investigator payments across clinical studies, ensuring accuracy and compliance. They also coordinate with vendors, resolve payment discrepancies, and support audit activities to maintain operational efficiency.

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Investigator Payments Lead

ICON plc · Full Time · 1 hour ago

ICON plc

🌎 Bulgaria, Poland, Spain ⭐ 2-5 yrs exp 💼 Others

The Investigator Payments Lead manages end-to-end clinical trial site payment activities, ensuring accuracy and compliance with contractual agreements. They oversee payment system configurations, monitor vendor performance, and resolve payment-related queries to support study delivery.

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Sales Key Account Manager Oncology - Außendienst - Region "Mitte"

Johnson & Johnson Innovative Medicine · Full Time · 1 hour ago

Johnson & Johnson Innovative Medicine

🌎 Austria 💵 €62200 - €99935 per year ⭐ 2-5 yrs exp 💼 Sales Key Account Manager

The Key Account Manager drives sales and business results by executing brand plans and maintaining partnerships within the oncology and hematology therapeutic areas. They act as a product specialist, analyzing territory data to develop account plans and coordinating cross-functional activities to ensure customer interaction excellence.

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Sr CRA (Level I)

Thermo Fisher Scientific · Full Time · 1 hour ago

Thermo Fisher Scientific

🌎 United States ⭐ 2-5 yrs exp 💼 Others

The Senior CRA manages clinical monitoring and site management activities to ensure trials are conducted according to protocols, ICH-GCP, and regulatory requirements. They perform remote and on-site monitoring, conduct data verification, and maintain effective communication with investigational sites to ensure data quality and patient safety.

medical clinical-research communication microsoft-office medical-terminology

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Investigator Payments Lead, Senior Associate - FSP

Parexel · Full Time · 1 hour ago

Parexel

🌎 Argentina ⭐ 2-5 yrs exp 💼 Others

The Investigator Payments Lead manages the end-to-end lifecycle of clinical site payments, ensuring timely and accurate disbursements from study startup to close. They also provide oversight of vendor staff and troubleshoot complex payment issues to maintain site satisfaction and contractual compliance.

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Clinical Trial Associate

ICON plc · Full Time · 2 hours ago

ICON plc

🌎 South Korea ⭐ 2-5 yrs exp 💼 Healthcare

The Clinical Trial Associate assists project teams with the setup, organization, and maintenance of clinical study documentation and trial materials. They also perform quality control audits, track trial progress, and serve as a primary contact for clinical sites regarding basic requests.

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Laboratory Study Manager

ICON plc · Full Time · 2 hours ago

ICON plc

🌎 Bulgaria, Lithuania, Oman, Poland, Romania ⭐ 5-10 yrs exp 💼 Others

The Laboratory Study Manager will lead the planning, execution, and monitoring of complex clinical trials while ensuring adherence to regulatory requirements. They will collaborate with cross-functional teams to manage study plans, budgets, and timelines while resolving complex issues to maintain data integrity.

medical clinical-research communication training

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Clinical Research Associate - Poznan - FSP

Parexel · Full Time · 2 hours 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.

security clinical-research science talent-acquisition

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Local Contract Research Nurse (Per Diem) - Naples, Italy

Syneos Health · Part Time · 3 hours ago

Syneos Health

🌎 Italy ⭐ 2-5 yrs exp 💼 Healthcare

The Research Nurse will coordinate patient care and facilitate communication between patients and healthcare providers to ensure study protocol compliance. They are responsible for monitoring patient progress, collecting accurate data, and providing individualized support throughout the clinical research process.

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Site Management Associate

ICON plc · Full Time · 4 hours ago

ICON plc

🌎 Thailand ⭐ 0-2 yrs exp 💼 Others

The Site Management Associate supports clinical trial site management by assisting with monitoring activities and ensuring adherence to study protocols and regulatory requirements. They also collaborate with cross-functional teams to maintain accurate records and facilitate effective site communication.

clinical-research communication training documentation compliance

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Senior Contract Associate

BeiGene · Full Time · 4 hours ago

BeiGene

🌎 Germany 💵 €69800 - €87200 per year ⭐ 2-5 yrs exp 💼 Others

The Senior Contract Associate is responsible for drafting, negotiating, and finalizing complex clinical site contracts and budgets throughout the study lifecycle. They serve as the primary point of contact between internal departments and external sites to ensure compliance and timely execution of agreements.

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CRA II

Thermo Fisher Scientific · Full Time · 4 hours ago

Thermo Fisher Scientific

🌎 South Korea ⭐ 2-5 yrs exp 💼 Others

The Clinical Research Associate II coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence, manage documentation, and resolve site-level issues.

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Senior Technology Auditor, QA

Parexel · Full Time · 5 hours ago

Parexel

🌎 India ⭐ 5-10 yrs exp 💼 Finance Auditor

Lead, perform, and report a range of GxP audits across all phases of clinical research to ensure compliance with regulatory requirements. Manage audit programs, coordinate internal audits, and provide consultancy on quality and regulatory compliance to internal and external stakeholders.

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CRAII/ Sr CRAI (sponsor dedicated) Athens

Syneos Health · Full Time · 5 hours ago

Syneos Health

🌎 Greece ⭐ 2-5 yrs exp 💼 Others

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams and investigators to manage project components and ensure accurate documentation of monitoring activities.

clinical-research agile communication microsoft-office training documentation organization

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Central Review Manager

Thermo Fisher Scientific · Full Time · 7 hours ago

Thermo Fisher Scientific

🌎 India ⭐ 2-5 yrs exp 💼 Others

The Central Review Manager performs centralized review and approval of clinical monitoring visit reports to ensure consistency and protocol compliance. They also liaise with clinical monitoring staff and evaluate site performance, subject safety, and study processes based on monitoring data.

medical english clinical-research communication training time-management medical-terminology

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Computational Statistician (R2-R3)

Lilly · Full Time · 8 hours ago

Lilly

🌎 United States 💵 $79206 - $134K per year ⭐ 0-2 yrs exp 💼 Software Development

The Computational Statistician will develop and implement statistical analysis plans for clinical trials while collaborating with clinical research associates. They are responsible for establishing reporting databases, conducting peer reviews, and ensuring the accuracy of statistical analyses.

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Clinical Research Physician - Malignant Hematology

Lilly · Full Time · 8 hours ago

Lilly

🌎 United States 💵 $198K - $389K per year ⭐ 2-5 yrs exp 💼 Healthcare

The Clinical Research Physician participates in the development, conduct, and reporting of global clinical trials to support product registration and commercialization. They serve as a scientific resource for study teams, ensuring compliance with regulatory standards and managing medical strategies for marketed compounds.

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Clinical Research Lead - Immunology, Investigator Engagement (CA-West Coast Region)

Lilly · Full Time · 8 hours ago

Lilly

🌎 United States 💵 $115K - $187K per year ⭐ 5-10 yrs exp 💼 Healthcare

The Clinical Research Lead is responsible for driving clinical trial execution through strategic investigator engagement and site performance management. They act as a scientific ambassador to ensure protocol understanding and optimize enrollment strategies across the West Coast region.

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Clin Ops Specialist - Beijing

Syneos Health · Full Time · 9 hours ago

Syneos Health

🌎 China ⭐ 0-2 yrs exp 💼 Others

The Clinical Operations Specialist is responsible for ensuring site compliance with clinical protocols and maintaining accurate trial documentation. They also assist clinical monitoring staff with site management activities and coordinate essential project supplies and team meetings.

clinical-research agile communication operations training organization compliance

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Sr Project Manager - Beijing/Shanghai

Syneos Health · Full Time · 9 hours ago

Syneos Health

🌎 China ⭐ 5-10 yrs exp 💼 Product Project Manager

The Senior Project Manager oversees interdisciplinary clinical research programs, ensuring compliance with regulatory requirements and GCP standards. They act as the primary liaison between the company and customers to manage project deliverables, timelines, and budgets.

clinical-research project-management agile training leadership organization compliance

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Central Risk Manager (RBQM & Central Monitoring) - Remote: United States or Canada

Syneos Health · Full Time · 12 hours ago

Syneos Health

🌎 Spain 💵 $95000 - $175K per year ⭐ 10+ yrs exp 💼 Finance Risk Manager

The Central Risk Manager will serve as a subject matter expert in RBQM and centralized monitoring, leading risk assessments and developing monitoring strategies for global clinical trials. They will partner with sponsors and cross-functional teams to drive data-driven decision-making and ensure study quality and patient safety.

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FSP- Sr CRA II (Melbourne/ Sydney)

Syneos Health · Full Time · 12 hours ago

Syneos Health

🌎 Australia ⭐ 5-10 yrs exp 💼 Others

The Senior CRA II conducts on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. They also provide mentorship to junior staff, develop monitoring tools, and collaborate with cross-functional teams to ensure successful trial execution.

clinical-research agile communication feedback training documentation organization

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Director of Nursing

START Center for Cancer Research · Full Time · 13 hours ago

START Center for Cancer Research

🌎 United States 💵 $195K - $205K per year ⭐ 10+ yrs exp 💼 Others

The Director of Nursing provides proactive leadership and supervision to clinical staff, including nurses, navigators, and intake coordinators. They ensure high-quality patient care, regulatory compliance, and efficient operational workflows across all clinical research departments.

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Global Trial Optimization Specialist

ICON plc · Full Time · 13 hours ago

ICON plc

🌎 United States ⭐ 2-5 yrs exp 💼 Others

Develop and implement strategic patient recruitment and retention plans to ensure clinical trials meet their timelines. Serve as an expert consultant to project teams and manage vendor relationships to support study objectives.

clinical-research data-analysis communication reporting training time-management

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Director of Nursing

START Center for Cancer Research · Full Time · 14 hours ago

START Center for Cancer Research

🌎 United States 💵 $175K - $185K per year ⭐ 10+ yrs exp 💼 Others

The Director of Nursing provides leadership and supervision to clinical staff, ensuring high-quality patient care and adherence to research protocols. They are responsible for staff training, process improvement, and inter-departmental coordination to support clinical trial enrollment and regulatory compliance.