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 (1,576)

Medical Science Liaison, France

Revolution Medicines · Full Time · 1 Week Ago

Revolution Medicines

🌎 France ⭐ 10+ yrs exp 💼 Healthcare

The MSL will execute field medical plans in France by engaging in scientific dialogue with healthcare professionals and cultivating relationships with Key Opinion Leaders. They will serve as a therapeutic expert and liaison between the company and clinical study sites to support medical education and congresses.

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Senior Clinical Research Associate

PSI CRO · Full Time · 1 Week Ago

PSI CRO

🌎 Gambia ⭐ 5-10 yrs exp 💼 Healthcare

The Senior Clinical Research Associate will conduct onsite monitoring visits, manage site communications, and ensure data quality and compliance for clinical research projects. They will also supervise study activities, timelines, and support regulatory document preparation for various therapeutic indications.

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Clinical Trial Manager II

ICON plc · Full Time · 1 Week Ago

ICON plc

🌎 Turkey ⭐ 5-10 yrs exp 💼 Healthcare

Oversee clinical trial management workstreams to ensure deliverables meet quality and timeline expectations. This includes designing protocols, managing day-to-day operations, and analyzing clinical data to optimize study outcomes.

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Biosampling Project Manager

ICON plc · Full Time · 1 Week Ago

ICON plc

🌎 Bulgaria, Oman, Romania ⭐ 5-10 yrs exp 💼 Product Project Manager

You will lead the planning, execution, and monitoring of complex clinical trials while ensuring adherence to regulatory requirements and project timelines. Additionally, you will collaborate with cross-functional teams to manage study plans, budgets, and resolve intricate operational challenges.

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Laboratory Study Manager

ICON plc · Full Time · 1 Week Ago

ICON plc

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

You will lead and coordinate central laboratory activities, acting as the primary link between study teams and laboratory partners. Responsibilities include managing human biological samples, overseeing laboratory operations, and ensuring compliance with global clinical study requirements.

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Community Associate

Careers at Eucalyptus · Full Time · 1 Week Ago

Careers at Eucalyptus

🌎 South Africa ⭐ 2-5 yrs exp 💼 Others

Manage the day-to-day operations of an online community by building member relationships and moderating content. Collaborate with cross-functional teams to triage patient communications and use community data to improve member engagement.

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Study Start Up Associate II

ICON plc · Full Time · 1 Week Ago

ICON plc

🌎 Denmark, Norway ⭐ 2-5 yrs exp 💼 Others

Lead the initiation and activation of clinical trials by managing the collection and review of essential site documents. Collaborate with internal teams and CROs to improve start-up metrics and ensure compliance with regulatory requirements.

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In-House Clinical Research Associate - Poland or Serbia

Worldwide Clinical Trials · Full Time · 1 Week Ago

Worldwide Clinical Trials

🌎 Poland, Serbia ⭐ 0-2 yrs exp 💼 Healthcare

Ensure the quality and timely submission of study site data and safety reporting. Manage regulatory documentation, ethical submissions, and Trial Master File updates while performing site feasibility studies.

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In-House Clinical Research Associate - Spain

Worldwide Clinical Trials · Full Time · 1 Week Ago

Worldwide Clinical Trials

🌎 Spain ⭐ 0-2 yrs exp 💼 Healthcare

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Study Start Up Associate II

ICON plc · Full Time · 1 Week Ago

ICON plc

🌎 Spain ⭐ 2-5 yrs exp 💼 Others

Lead the initiation of clinical trials by managing site start-up and activation activities. Ensure compliance with regulatory requirements and maintain the accuracy of essential documents within the eTMF.

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Operations Finance Data & Reporting Analyst I - Bulgaria - Remote

Worldwide Clinical Trials · Full Time · 1 Week Ago

Worldwide Clinical Trials

🌎 Bulgaria ⭐ 0-2 yrs exp 💼 Finance

The analyst will prepare financial metrics and reports for internal management while enhancing business tools to automate processes. Key duties include project setup, ERP data integrity maintenance, and managing the timekeeping and billing processes.

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Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)

Thermo Fisher Scientific · Full Time · 1 Week Ago

Thermo Fisher Scientific

🌎 Germany ⭐ 0-2 yrs exp 💼 Healthcare

The CRA I coordinates clinical monitoring and site management to ensure protocol and regulatory compliance. They conduct site visits, manage documentation, and maintain collaborative relationships with investigational sites to guarantee data reliability.

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Senior Clinical Research Associate

Ergomed · Full Time · 1 Week Ago

Ergomed

🌎 United States ⭐ 5-10 yrs exp 💼 Healthcare

The role involves performing on-site or remote monitoring visits to ensure investigational sites are adequate for clinical study conduct. Responsibilities include training site staff, verifying investigator qualifications, and mentoring junior staff through co-monitoring visits.

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Clin Ops Specialist

Syneos Health · Full Time · 1 Week Ago

Syneos Health

🌎 South Korea ⭐ 0-2 yrs exp 💼 Others

The specialist supports clinical monitoring staff with site management and ensures compliance with protocol requirements and guidelines. They are also responsible for maintaining the Trial Master File, tracking regulatory documents, and coordinating site supplies.

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Director, Operational Efficiency & Technology Innovation (United Kingdom)

MMS · Full Time · 1 Week Ago

MMS

🌎 United Kingdom ⭐ 10+ yrs exp 💼 Others

The role focuses on advancing AI and emerging technologies to improve operational efficiency, quality, and business outcomes across all service lines. It involves establishing AI governance frameworks and partnering with cross-functional leaders to drive technology adoption and organizational change.

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Clinical Trial Manager (Study Start Up CTM)

ICON plc · Full Time · 1 Week Ago

ICON plc

🌎 Taiwan ⭐ 5-10 yrs exp 💼 Healthcare

Manage day-to-day clinical trial operations, ensuring adherence to timelines, budgets, and quality standards. Collaborate with cross-functional teams and investigators to implement protocols in compliance with international regulations.

clinical-research operations training compliance

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Site Contracts Negotiator

ICON plc · Full Time · 1 Week Ago

ICON plc

🌎 India ⭐ 2-5 yrs exp 💼 Others

The role involves independently managing the negotiation and execution of clinical trial agreements and budgets for various studies. Key duties include collaborating with internal stakeholders and sites to ensure compliant and efficient study start-up.

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Senior Clinical Research Associate - Oncology, Rare Disease - Japan

Worldwide Clinical Trials · Full Time · 1 Week Ago

Worldwide Clinical Trials

🌎 Sweden ⭐ 2-5 yrs exp 💼 Healthcare

The CRA is responsible for managing the full lifecycle of study sites, including qualification, initiation, monitoring, and close-out. They ensure protocol adherence, verify source documents for data veracity, and provide guidance to site staff and junior CRAs.

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Sr CRA I - Guangzhou

Syneos Health · Full Time · 1 Week Ago

Syneos Health

🌎 China ⭐ 2-5 yrs exp 💼 Others

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory requirements. Develop quality monitoring tools and collaborate with cross-functional teams to support clinical trial operations.

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eClinical Business Lead, UAT Lead

Parexel · Full Time · 1 Week Ago

Parexel

🌎 India ⭐ 5-10 yrs exp 💼 Others

Oversee and manage the delivery of User Acceptance Testing (UAT) for eClinical vendor systems including IRT, eCOA, and ePRO. Collaborate with cross-functional teams and sponsors to ensure technology solutions meet project requirements and regulatory standards.

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CRA - FSP - Italy

Thermo Fisher Scientific · Full Time · 1 Week Ago

Thermo Fisher Scientific

🌎 Italy ⭐ 2-5 yrs exp 💼 Others

Monitor investigator sites using a risk-based approach to ensure data accuracy and compliance with protocols and regulatory requirements. Manage site initiation, close-out, and maintain regular communication with investigative sites to resolve deficiencies.

medical english clinical-research communication microsoft-office critical-thinking science

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Project Manager / Clinical Trial Lead - sponsor dedicated - Germany

Syneos Health · Full Time · 1 Week Ago

Syneos Health

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

The role involves leading and managing global clinical trials to ensure quality execution, compliance with GCP, and adherence to budgets and timelines. The Project Manager acts as the primary liaison between the company and the customer while overseeing interdisciplinary research studies.

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Directeur médical, neurologue

IQVIA · Full Time · 1 Week Ago

IQVIA

🌎 Canada 💵 $155K - $289K per year ⭐ 2-5 yrs exp 💼 Others

The Medical Director serves as the medical expert for clinical trials focusing on neurological diseases, primarily handling medical monitoring and scientific advisory. They are responsible for protocol-related support, analyzing adverse events, and contributing to the medical strategy of client proposals.

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Regional Clinical Trial Manager

ICON plc · Full Time · 1 Week Ago

ICON plc

🌎 Taiwan ⭐ 5-10 yrs exp 💼 Healthcare

Manage day-to-day clinical trial operations, ensuring adherence to timelines, budgets, and quality standards. Collaborate with cross-functional teams and stakeholders to implement protocols and ensure regulatory compliance.

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FSP CRA (Level II)

Thermo Fisher Scientific · Full Time · 1 Week Ago

Thermo Fisher Scientific

🌎 China ⭐ 0-2 yrs exp 💼 Others

Performs clinical monitoring and site management to ensure protocol and regulatory compliance. Conducts remote or on-site visits to assess data reliability and maintain audit readiness.

medical english clinical-research communication microsoft-office critical-thinking science

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Project Manager II and PM I

Fortrea · Full Time · 1 Week Ago

Fortrea

🌎 United Kingdom ⭐ 2-5 yrs exp 💼 Product Project Manager

Lead the end-to-end delivery of Healthy Volunteers and Patient Clinical Pharmacology projects while managing sponsor relationships and project budgets. Ensure quality, compliance, and audit readiness according to SOPs and ICH/GCP standards within a matrix environment.

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Senior Manager, Site Relationships and Engagement

ICON plc · Full Time · 1 Week Ago

ICON plc

🌎 United States ⭐ 5-10 yrs exp 💼 Others

Lead the strategy and execution of Oncology site network development and relationship management for clinical trials. Collaborate with cross-functional teams to enhance bid scenarios and monitor post-award delivery to ensure timely trial start-up.

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Principal Clinical Data Standards Consultant

ICON plc · Full Time · 1 Week Ago

ICON plc

🌎 China ⭐ 10+ yrs exp 💼 Healthcare

The role involves developing and maintaining clinical data collection standards libraries in compliance with CDISC and regulatory requirements. The consultant will act as a subject matter expert for studies in China and provide guidance on standards implementation across clinical data management activities.

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Senior Clinical Project Manager or Project Manager II - Oncology

Fortrea · Full Time · 1 Week Ago

Fortrea

🌎 United States ⭐ 5-10 yrs exp 💼 Product Project Manager

The Senior Project Manager oversees domestic and global oncology projects, managing teams, budgets, risks, and stakeholder communications to ensure operational excellence. They are also responsible for regulatory documentation, line management of staff, and supporting business development efforts.

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Study Start Up Associate - Medical Device

ICON plc · Full Time · 1 Week Ago

ICON plc

🌎 United States ⭐ 2-5 yrs exp 💼 Healthcare

The SSU Associate coordinates clinical trial site start-up activities, focusing on the preparation, submission, and approval of regulatory documents and Informed Consent Forms. They manage site readiness, track metrics in CTMS and eTMF, and ensure compliance with global regulatory standards.

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