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 (1,605)

Senior Specialist, Clinical Research Monitoring

Edwards Lifesciences · Full Time · 3 Weeks Ago

Edwards Lifesciences

🌎 Georgia 💵 $108K - $153K per year ⭐ 5-10 yrs exp 💼 Healthcare

Perform field monitoring of clinical trials to ensure data consistency and compliance with GCP and regulatory requirements. Provide oversight of trial activities, mentor junior staff, and contribute to the development of clinical protocols and informed consent forms.

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Manager, Clinical Research Monitoring

Edwards Lifesciences · Full Time · 3 Weeks Ago

Edwards Lifesciences

🌎 Georgia 💵 $126K - $178K per year ⭐ 5-10 yrs exp 💼 Healthcare

Lead field monitoring and data collection for complex clinical trials while ensuring compliance with GCP and regulatory requirements. Provide strategic direction, mentor junior staff, and oversee trial conduct including metrics and protocol deviations.

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Community IBC Member (Augusta)

Sitero LLC · Full Time · 3 Weeks Ago

Sitero LLC

🌎 United States 💵 $110 - $125 per day ⭐ 5-10 yrs exp 💼 Others

The member reviews research protocols and monitors regulatory compliance to ensure the protection of participants, animals, and biosafety standards. They provide recommendations for the approval or termination of studies and assess risks associated with hazardous biological work.

clinical-research training compliance

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CRA II and SR CRA

ICON plc · Full Time · 3 Weeks Ago

ICON plc

🌎 Brazil ⭐ 2-5 yrs exp 💼 Others

Coordinate and execute clinical trial monitoring activities, including site visits and study status reporting. Maintain strong relationships with stakeholders and ensure patient safety through strict compliance with protocols and regulatory requirements.

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Vice President, Imaging

ICON plc · Full Time · 3 Weeks Ago

ICON plc

🌎 Ireland, United States ⭐ 10+ yrs exp 💼 Others

Serve as a senior strategic leader driving business growth and strengthening sponsor relationships within medical imaging and cardiac safety services. Provide expert guidance on study strategy, operational delivery, and scientific innovation for global clinical development programs.

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Community IBC Member (Nashville, TN)

Sitero LLC · Full Time · 3 Weeks Ago

Sitero LLC

🌎 United States 💵 $110 - $125 per year ⭐ 5-10 yrs exp 💼 Others

The member reviews research protocols and monitors regulatory compliance to ensure the protection of participants, animals, and data integrity. They specifically assess biosafety standards and provide recommendations for the approval or termination of studies.

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Sr Clinical Research Associate

Veranex, Inc. · Full Time · 3 Weeks Ago

Veranex, Inc.

🌎 United States 💵 $98400 - $140K per year ⭐ 5-10 yrs exp 💼 Healthcare

The Sr. CRA is responsible for monitoring clinical trials to ensure adherence to protocols, regulations, and SOPs while acting as the primary liaison to clinical sites. Key duties include conducting site visits, verifying source data, and contributing to the development of study plans and regulatory reports.

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Senior Statistical Programmer

Everest Clinical Research · Full Time · 3 Weeks Ago

Everest Clinical Research

🌎 United Kingdom ⭐ 5-10 yrs exp 💼 Software Development

Design and specify study data tabulation and analysis models for clinical trials in accordance with industry standards. Develop SAS programming codes to generate accurate statistical output reports and provide technical guidance to junior programmers.

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Project Manager, Contracts & Operations

Lupus Research Alliance Inc. · Full Time · 3 Weeks Ago

Lupus Research Alliance Inc.

🌎 United States 💵 $75000 - $85000 per year ⭐ 2-5 yrs exp 💼 Product Project Manager

The role involves managing cross-functional projects and administering the contracting process for Lupus Therapeutics. Key duties include preparing agreements, tracking budgets, and coordinating with biopharmaceutical partners and outside counsel.

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Senior Proposals Development Associate

ICON plc · Full Time · 3 Weeks Ago

ICON plc

🌎 United States ⭐ 5-10 yrs exp 💼 Others

Facilitate the development and preparation of high-quality proposals for clinical trials by collaborating with cross-functional teams and subject matter experts. Manage timelines, ensure compliance with client requirements, and mentor colleagues in the proposal process.

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Senior Site Contract Associate - IQVIA Biotech

IQVIA · Full Time · 3 Weeks Ago

IQVIA

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

Manage start-up contracting activities, including the development of investigator grant estimates and proposal text for biotech sponsors. Ensure overall contracting efficiency and adherence to project timelines while maintaining internal systems like CTMS.

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Auditor/Educator Physician

Omega Healthcare Solutions · Full Time · 3 Weeks Ago

Omega Healthcare Solutions

🌎 United States 💵 $35.5 - $51.5 per hour ⭐ 5-10 yrs exp 💼 Finance Auditor

The Auditor/Educator Physician reviews medical records for coding accuracy and provides feedback and education to improve documentation. They also create action plans and training materials to address coding problems and documentation gaps.

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Auditor/Educator In/Outpatient

Omega Healthcare Solutions · Full Time · 3 Weeks Ago

Omega Healthcare Solutions

🌎 United States 💵 $38.5 - $58 per hour ⭐ 5-10 yrs exp 💼 Finance Auditor

Review medical records for coding accuracy and provide feedback to coders and providers. Deliver education to improve documentation and coding practices.

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Medical Science Liaison, Global Rare Diseases - Midwest

Chiesi Group · Full Time · 3 Weeks Ago

Chiesi Group

🌎 United States 💵 $142K - $173K per year ⭐ 2-5 yrs exp 💼 Healthcare

The Medical Science Liaison (MSL) is responsible for building partnerships with key opinion leaders and engaging in scientific exchanges with external stakeholders. This includes providing medical support, delivering education, and fostering collaborations in the assigned therapeutic areas.

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Clinical Research Associate

ICON plc · Full Time · 3 Weeks Ago

ICON plc

🌎 United States 💵 $91336 - $114K per year ⭐ 2-5 yrs exp 💼 Healthcare

The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for early-stage development clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.

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RBSM - Lead

ICON plc · Full Time · 3 Weeks Ago

ICON plc

🌎 United Kingdom ⭐ 5-10 yrs exp 💼 Others

Provide end-to-end risk oversight for clinical studies to ensure patient safety, data quality, and trial integrity. Lead cross-functional risk review meetings and collaborate with Clinical Research Managers to implement mitigation strategies.

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Tech Systems/Support Analyst - Hungarian Native (Portugal Homebased)

IQVIA · Full Time · 3 Weeks Ago

IQVIA

🌎 Portugal ⭐ 0-2 yrs exp 💼 Support

The Tech/System Analyst provides first-level support to Clinical Trials personnel via phone, email, and chat. They ensure timely resolution of technical and operational inquiries.

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Associate Manager - Safety Operations

IQVIA · Full Time · 3 Weeks Ago

IQVIA

🌎 Argentina, Mexico ⭐ 2-5 yrs exp 💼 Others

Manage Medical Information staff and support operational decisions as directed by senior management. Collaborate with stakeholders to achieve local and global deliverables and metrics.

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Solutions Design Analyst

Clario · Full Time · 3 Weeks Ago

Clario

🌎 Costa Rica ⭐ 2-5 yrs exp 💼 Design

The analyst is responsible for delivering high-quality eCOA solution designs by translating pharmaceutical client requirements and study protocols into optimized specifications. They coordinate the design process and collaborate with cross-functional teams to ensure data integrity and efficient project delivery.

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FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc

Fortrea · Full Time · 3 Weeks Ago

Fortrea

🌎 United States 💵 $125K - $140K per year ⭐ 5-10 yrs exp 💼 Healthcare

Responsible for all aspects of clinical site monitoring, including initiation, routine visits, and close-out of oncology trials. Ensures data integrity, patient safety, and adherence to study protocols and regulatory requirements.

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FSP Principal Medical Writer (Regulatory) - Client-Dedicated

Thermo Fisher Scientific · Full Time · 3 Weeks Ago

Thermo Fisher Scientific

🌎 France, Greece, Italy, Portugal, United Kingdom ⭐ 10+ yrs exp 💼 Legal Medical Writer

Lead the planning, writing, and delivery of high-quality clinical and regulatory documents such as CSRs, protocols, and IBs. Provide subject matter expertise on document strategy and mentor junior medical writers to ensure operational excellence.

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Lead Medical Project Coord

Thermo Fisher Scientific · Full Time · 3 Weeks Ago

Thermo Fisher Scientific

🌎 Philippines ⭐ 10+ yrs exp 💼 Healthcare

Lead the management and coordination of medical projects to ensure compliance and optimal performance throughout the project lifecycle. Perform safety data reviews, manage project financials, and serve as the primary point of contact for clinical project teams.

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Medical Project Coordinator

Thermo Fisher Scientific · Full Time · 3 Weeks Ago

Thermo Fisher Scientific

🌎 Philippines ⭐ 2-5 yrs exp 💼 Product Project Coordinator

Coordinate and review safety data to ensure compliance with regulatory standards and optimal patient safety in clinical trials. Identify safety trends, resolve complex issues, and support the creation of safety and medical management plans.

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Senior Medical Project Coordinator

Thermo Fisher Scientific · Full Time · 3 Weeks Ago

Thermo Fisher Scientific

🌎 Philippines ⭐ 5-10 yrs exp 💼 Product Project Coordinator

The Senior Medical Project Coordinator manages and evaluates medical projects to ensure compliance, alignment, and optimal performance throughout the project lifecycle. This includes reviewing safety data, managing project financials, and serving as the primary point of contact for clinical project teams.

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Clinical Trial Manager with at least 5 years of experience in clinical research and experience as a CTM working with US - Mexico Home Based

Syneos Health · Full Time · 3 Weeks Ago

Syneos Health

🌎 Mexico ⭐ 5-10 yrs exp 💼 Healthcare

The role involves managing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires overseeing data integrity, investigational product reconciliation, and maintaining the Trial Master File.

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Coder Inpatient

Omega Healthcare Solutions · Full Time · 3 Weeks Ago

Omega Healthcare Solutions

🌎 United States 💵 $33.5 - $46 per hour ⭐ 2-5 yrs exp 💼 Software Development

The Coder Inpatient reviews medical records and performs coding on all diagnoses and procedures. They are responsible for maintaining the confidentiality of patient records while ensuring compliance with coding guidelines and regulations.

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VP Strategic Advisory Partnerships

Omega Healthcare Solutions · Full Time · 3 Weeks Ago

Omega Healthcare Solutions

🌎 United States 💵 $230K - $260K per year ⭐ 10+ yrs exp 💼 Others

The VP Strategic Advisory Partnerships will position Omega as a partner of choice within the advisory ecosystem and drive measurable revenue through influenced and co-developed sales opportunities. Responsibilities include developing relationships with advisory firms, identifying opportunities for collaboration, and enabling revenue generation through strategic partnerships.

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Supplier Performance Management Monitor

ICON plc · Full Time · 3 Weeks Ago

ICON plc

🌎 United States ⭐ 5-10 yrs exp 💼 Recruitment

Monitor the collection and analysis of data from third-party suppliers for sponsored clinical trials. Evaluate supplier compliance, track corrective actions, and maintain professional relationships with external stakeholders.

clinical-research communication training compliance

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Attorney 1, Securities

IQVIA · Full Time · 3 Weeks Ago

IQVIA

🌎 United States 💵 $77900 - $194K per year ⭐ 2-5 yrs exp 💼 Legal Attorney

The Attorney 1 will prepare SEC filings and provide counsel on compliance, governance, and capital markets transactions. They will also manage legal entity reorganizations and coordinate sustainability reporting requirements.

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Associate Director of Clinical Affairs

Harrow, Inc. · Full Time · 3 Weeks Ago

Harrow, Inc.

🌎 United States ⭐ 5-10 yrs exp 💼 Healthcare

The Associate Director of Clinical Affairs is responsible for creating and executing clinical strategies, including the design and support of clinical studies and protocol development. This role involves overseeing CROs and collaborating with cross-functional teams to facilitate trial enrollment and regulatory compliance.

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