US National Jobs - Remote, Work from Home, Part Time & Flexible Jobs
The U.S. probably has the highest number of remote and freelance jobs in the world. Many U.S. companies, from top-ranking Fortune 500 firms, such as Apple, 3M, Intel, Cisco, and MetLife, down to entrepreneurial startups, have strong... More
I lost my job due to COVID-19, but honestly, I already wanted a change. I was losing precious hours commuting and that took me away from my toddler and husband. Now I can focus on being productive and, when work is done, on being a wife and mom. I have a new outlook on life. I can actually have it all: a family and a career with work-life balance. I never intend to return to a job that isn't flexible. I'm really grateful and excited I made the choice to subscribe to FlexJobs!
I'd accomplished everything I wanted to in my last position and there was no chance of advancement. I also wanted to change to a career where I was helping others and hopefully increase my salary. Being able to work from home is a big plus. Being a single dad, it's nice not to commute to work, and it's easier to work additional hours when needed. I found FlexJobs' customizable search filters most effective in my search.
I was very unhappy at my previous job and am way more comfortable at home. I decided to look for a remote job and found FlexJobs! I've had this job for over a year now and it's been nothing short of amazing. I'm finally working a job where I am 100% comfortable, and I owe it all to FlexJobs. I'm able to keep up with my house and do other things during the day. My job is extremely flexible, and I had no idea how possible it is to find a remote job and actually excel.
FlexJobs is easy to navigate and has a lot of great tools. I'm so glad I took a chance and bought a membership. I needed to find another flexible, work-from-home position. My son has autism, and my job allows me to stay home and care for my son while earning a steady income. I have the option to work full-time when my availability allows for it. It's very important for my mental health. I can easily take time off and rearrange my schedule to accommodate my son's appointments. It's a perfect fit!
With my husband being active-duty military, I knew a remote job would be the only way for me to pursue a stable career. I found the perfect job and I'm so grateful I had FlexJobs to help me. For the price of a cheap lunch, you could potentially change your life. FlexJobs makes it possible to avoid work-from-home scams and find companies that fit your needs. I set up an email alert for my search criteria so I'd be alerted as soon as new jobs were added and tailored my resume for each position.
This job has made my life better. Every day, I work on something new, interesting, and challenging. I can balance my work with my life and have more control over my schedule. Many capable women in my generation have given up enriching careers because of children or household duties. With FlexJobs, everyone can find rewarding work that molds itself to their lifestyle. You'll never regret signing up for FlexJobs. Research the companies, customize your resumes and cover letters, and follow up.
Remote work is in such alignment with who I want to be as a husband and father. Having worked remotely due to COVID, I loved being able to create a better work-life balance and be more present for my family, and more productive professionally. Additionally, securing remote work will give us the flexibility to move closer to family and retain employment in my new role.
I'd been working virtually for years, but due to restructuring, my hours were cut. I still wanted a virtual job because I don't have to worry about bad weather and I like being home with my pets. My flexible job provides a better salary with less hours, and I can start and end my day when I like. The reason I think FlexJobs is the best service out there: they check on the companies posting to make sure they are legit, training is offered every week, and tests for skills are also helpful.
I'm a below-knee amputee and have recently had issues with my prosthesis but no financial resources to rectify them. I can still work, and working from home will provide discretionary income for a healthier diet and the ability to save. I can choose the schedule I prefer, as well as the range of hours I want to work. There are so many disabled adults who feel like they can no longer earn and/or contribute, but work-at-home positions can really enable them to enjoy life again.
We all tend to second-guess our abilities, but FlexJobs boosted my self-esteem. I've been a nurse for over 15 years and had been in search of a more flexible way to serve patients. I dabbled in travel and per diem nursing, but neither of those options truly gave me the flexibility I longed for, so I became a FlexJobs subscriber. Working remotely will aid me in sticking to a daily routine, will improve my overall health and well-being, and will prevent me from eating out every day.
My previous job was eliminated due to an acquisition, and I found the local job market was saturated. I knew commuting was not going to work for me, so I began looking on FlexJobs. Instead of commuting, I can take a short break and get started on homework for my online graduate program. Also, since my wife has an unconventional schedule, I can have lunch with her because of my flexible schedule. I can also get a morning workout in, and I get more work done remotely than I could in an office.
My disability made commuting difficult and requires that I sit in a reclined position. Also, my mother has Alzheimer's and cannot be left alone. For these reasons, I felt that getting a fully remote job was the best option for me. Having a remote job is life-changing! I no longer have to worry about the pain I had from commuting. As an added bonus, my hours are more flexible, so I can work when I'm feeling okay and rest when I need to, which reduces my anxiety and improves my overall health.
I was looking for a second part-time job to supplement my income, and I wanted it to be flexible so I could work it around my other job and do it from anywhere. I'll be able to pay off student loans faster, add writing pieces to my portfolio, and save time by not commuting. I can plan my job around my life, and I'm more confident about restarting my writing career knowing I can do it from anywhere around my current schedule. FlexJobs made it extremely easy for me to find work.
FlexJobs kept me motivated and gave me hope for a better role. I was able to get out of a toxic work environment and found a fantastic new job with a great team doing something I enjoy. The daily job email reminders kept me checking the boards every day. I've already seen the benefits of working remotely. It has not only allowed me to spend more time with family, but I'm able to see friends more and able to be more efficient with my time. FlexJobs is worth the price for the vetted positions.
FlexJobs was instrumental in my job search when I was laid off and needed to find 100% remote work. I have guardianship of two grandchildren who cannot attend school due to COVID-19, so I must be at home to help with their schooling and care. Working from home suits my personality, and I feel I accomplish more without the distractions of an office. I was very frustrated before using FlexJobs to find remote work. FlexJobs is a revelation.
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FeaturedNew! 2 days agoIndependently performs analytical testing, method optimization/validation, and/or other specialty technologies studies OR method transfers for pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or delivery systems.
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FeaturedNew! 2 days agoThe PL Is accountable for the overall delivery of the project (quality, time, cost) on behalf of the organization. Establishes and communicates customer expectations to the project team with minimal direction. Ensures that escalation pathways are...
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New! 2 days agoLeading or supporting scientific aspects of research activities in the following areas: research designs, methodologies, analytical techniques, data analyses, and reporting. Uses subject matter expertise in leading or supporting the development of...
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New! 5 days agoFunction in a lead role, meet with Vitalief's clinical research client stakeholders to assess their current clinical trials operational environment and understand what their business objectives are. Utilize business process improvement and change...
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8 days agoWrite and implement SAS macros and other utility tools. Independently designs and codes SAS programs for assigned project(s), consistently meeting objectives of the deliverables. Codes complex SAS programs to analyze and report clinical trial data.
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Featured9 days agoProvide medical consultation to team members and answer study related medical questions. Communicate clearly with associates and clients, maintaining and open line of communication to ensure all procedures are followed appropriately.
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9 days agoContributes to the development and/or review of study-related documentation, including but not limited to monitoring plan, risk management tool, eCRF, manuals, training materials, safety and regulatory documents, and clinical study report, etc.
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9 days agoSupport sales with clinical and technical demos of software products. Provide clinical guidance to sales, internal stakeholders, and customers as it relates to software. Collaborate with customers, sales, and customer success to define, document, and...
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10 days agoGuide all aspects of design, including visual design, interaction design, user experience, user research, and brand identity. Collaborate with cross-functional teams to develop design strategies that align with business goals and user needs. Develop...
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Featured10 days agoThe Senior Data Analyst will be responsible for implementing a range of moderate to complex analyses in support of clinical non-interventional studies (NIS)using collected data, such as chart reviews & prospective studies. PhD with at least 3 yrs of exp.
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11 days agoRepresent Development Operations on the Program Team (contribute to drug development strategy, planning, timing, cost projections) at the program level as well as the individual clinical study level. The Clinical Operations Lead is accountable to...
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Featured11 days agoParticipate in the design of complex multi-form CRFs and the resulting electronic databases. Lead the efforts for data cleaning, editing, and validation. Implement variable derivation, conduct statistical analyses for the types of studies described...
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Featured11 days agoServes as the primary contact and lead between the sponsor and the organization at the project level.Drives and owns the overall delivery of the cross-functional project (time, cost, quality).Establishes, communicates and manages customer expectations.
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Featured11 days agoServes as the primary contact and lead between the sponsor and the organization at the project level. On projects where the scope requires, ensures clear delineation in responsibilities and communication pathways for secondary project leads (such as...
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Featured11 days agoAccountable for the overall delivery of the project (quality, time, cost) on behalf of the organization. Establishes and communicates customer expectations to the project team with minimal direction. Ensures that escalation pathways are adhered to...
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16 days agoContinuously assess project status, reassess and revise risks, oversee issue documentation and escalation, and ensure the project team and stakeholders remain informed of project status, risks, and issues throughout the project (including both periodic...
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17 days agoPerform Lead Biostatistician role on medium complexity studies, providing statistical oversight and attending relevant project meetings. Perform project management activities for identified projects including resource planning, timelines and milestone...
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22 days ago5+ years of experience writing code using SQL or SAS to manipulate and analyze large government and/or commercial healthcare claims datasets. Proficiency executing observational/outcomes research studies and custom analytic engagements using large...
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22 days agoIn this role, the Senior Researcher is responsible for conceptualizing the vision for this work, providing support for project teams in developing and carrying out the work, following sound project management practices to ensure the timely completion...
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23 days agoAct as lead trial Biostatistician to provide statistical support for clinical studies in the study design, analysis, interpretation, and publication of clinical studies. Co-author protocols, statistical analysis plan, study reports, presentations, and...
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Featured24 days agoLeading of all medical aspects of contracted tasks. Supervising of safety variables. Discussing with clients, investigators and healthcare professionals of medical issues in the pre and post approval services by using accurate medical judgment...
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Featured24 days agoServe as a key BPS Subject Matter Expert (SME) by providing technical and strategic leadership for the development of biologics such as monoclonal antibodies. Lead the technical due diligence process when working with prospective customers as well...
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Featured24 days agoDay to day tasks include; drafting of work scopes and timelines, interacts with clients and internal project team members, and contributes to critical strategic thinking. Supports scientific coordination and project management, including scoping...
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25 days agoManages all clinical operational aspects of a clinical trial from site selection, start-up, enrollment, maintenance, and close-out. Prepares and reviews study related plans and documents including protocols, informed consent forms, recruitment plans...
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25 days agoProvide programming/study start up management or other support and assist CDM managers in daily technical operations. Respond to & solve technical oriented problems in a timely manner, as appropriate for the position. Plan, manage, execute and oversee...
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Featured25 days agoBe scientifically responsible person for design and implementation of selected Non-interventional studies; conceptualize methodologically sound advanced study designs to meet project objectives and develop/supervise the development of study protocols...
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Featured25 days agoWhen needed, the Senior Statistician will provide statistical as well as programming expertise. Responsibilities also include direct contributions to client proposals and study execution for the ESA business, including a variety of prospective and...
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25 days agoResponsibilities include conducting literature/evidence reviews, drafting new measure specifications, coordinating measure testing activities, monitoring and evaluating measure deployment, identifying publication opportunities, and maintaining...
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25 days agoManage complex programs, including strategy, timelines and internal and external stakeholder management, and drive value to ensure we're exceeding client expectations by: Maintaining strong relationships with both executives and project teams across...
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25 days agoContribute to business development of the Center by finding new opportunities and leading proposals for government and foundation clients under tight deadlines. Help advance methods and address key research questions on electronic nicotine devices and...
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25 days agoAs a scientific leader, identify new or adjacent business markets, meet with prospective clients identify strategic opportunities, lead capture and proposal development teams. As a scientific/technical leader, lead or support complex research projects.
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25 days agoCollaborate with team members to review patient recruitment and DCT strategies' appropriateness and implementation for various client proposals. 3-4 years' experience in Patient Recruitment for clinical research. Minimum Bachelor's degree.
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Featured26 days agoProvides scientific leadership to Outcomes Research team members. Maintains line of research and expertise in relevant scientific areas, along with connections with new literature and regulatory documents. Publishes scientific work in journals...
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26 days agoSupport clinical study teams for assigned studies through attendance at study meetings, review of study documents, and consultation on GCP-related questions. Identify and escalate significant compliance issues to Clinical QA and other relevant...
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Featured26 days agoProvide study, project and program-specific medical monitoring and review services, including but not restricted to: Leading of all medical aspects of contracted tasks. Supervising of safety variables. Discussing with clients, investigators and...
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26 days agoAct as project director and manage all aspects of systematic literature reviews (SLRs) and/or evidence synthesis (NMAs. ITCs) to ensure the quality of all deliverables meets client requirements. Establish and maintain client relationships.
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26 days agoThe Lead Consultant will manage projects and is expected to provide expertise relating to the critical review of relevant literature to inform model conceptualisation, design and parameterisation. They will also contribute to the programming of dynamic...
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29 days agoResearch medical literature to build Bayesian Networks holding expert medical knowledge. Collaborate with data scientists, med consultants, and software engineers. Take part in the quality assurance of Bayesian Networks content. Develop a platform.
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30+ days agoAs a Lead Data Manager you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. Must have demonstrated experience in providing customer-focused support, with satisfactory examples...
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30+ days agoDaily work activities may include developing communications plans to tell stories about research advancements, consulting on top-tier media inquiries, working with senior scientists to summarize and/or report on research papers, and writing or editing...
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30+ days agoConduct literature reviews to understand evidence-based guidelines across various conditions and procedures. Develop and validate measures using technical tools and claims data. Maintain a library of documentation for internal and external stakeholders.
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30+ days agoOverall responsibility for the design and execution of multiple clinical studies from inception through close-out with responsibility for all study components. Provides leadership to the internal study team and vendors to ensure work quality, execution...
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30+ days agoCollaborate with the medical writing team in the preparation and QC of the above documents.Liaise with internal and external clients in tracking status. Maintains SOPs and updates requirements based on current regulatory guidelines.Engages team members
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30+ days agoDevelop, implement, and manage scientific programs, initiatives, and events to advance priority areas. Clinical Trials: metastatic and aggressive breast cancers, breast cancer disparities and big data. These may include programs co-created with...
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30+ days agoDrive material compliance to applicable global product and/or packaging regulatory/environmental legislations (e.g. California Prop 65, RoHS, Conflict Minerals, EU Medical Device Regulation) for product portfolios. With minimal support, develop...
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30+ days agoDevelop and Manage a team of Epidemiologists, Biostatisticians, HEOR scientists, and related quantitative sciences that provide scientific expertise to our Real World Evidence, Clinical Research, and International Business Units, and proactively drive...
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30+ days ago5+ years of industry or equivalent experience, including observational or clinical research experience, preferably in rare diseases; must have experience in study design and conduct, as well as the analysis, interpretation, and communication of data.
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30+ days agoMay lead or support a study or studies, depending on size/complexity. If lead, accountable for the clinical/scientific execution of the protocol. As the lead, will be responsible for the following: Clinical point of contact for scientific issues...
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30+ days agoManage site development and oversight activities including project planning, developing processes and tools, and overseeing, training, and mentoring staff in the conduct of, the following activities. Conduct site assessments, determine site needs...
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30+ days agoThe Clinical Project Manager (CPM) is responsible for the planning, implementation and conduct of single region or less complex, clinical trials in Phase I-III. The CPM is accountable for the day-to-day operations of clinical trials including, but not...
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