Bookkeeping Jobs - Remote Work From Home & Flexible
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.
Chris N.
from
Oregon City, OR United States — Hired at SureSwift Capital as Staff Accountant
Your site is fantastic. You have helped me make a change I really needed to make, and you made it so easy! Thank you! I am very grateful! FlexJobs was easy to use and really pinpointed the jobs that would be a good match for me. I'm a single mom of three that was working full-time, sometimes 70-80 hours a week. I found a job on this site that is 100 percent work-from-home and is a much better fit for me and my
kids!
Rachel B.
from
Cary, NC United States — Hired at Clevertech as Staff Accountant
FlexJobs is one job search site that gets it! I found a great telecommuting position in about two months. It is definitely worth the
money.
Natasha W.
from
Hagerstown, MD United States — Hired at AccountingDepartment.com as Bookkeeper
Welcome to remote, part-time, freelance, and flexible bookkeeping jobs! Bookkeeping professionals often work on a contract or freelance basis for small businesses or larger companies. Bookkeeping jobs are available in a variety of industries, such as nonprofit, sales, small business, art and creative, client services,... More
Welcome to remote, part-time, freelance, and flexible bookkeeping jobs! Bookkeeping professionals often work on a contract or freelance basis for small businesses or larger companies. Bookkeeping jobs are available in a variety of industries, such as nonprofit, sales, small business, art and creative, client services, and accounting and finance. Bookkeeping professionals should have an aptitude for organized and detailed work, and math and computer skills are essential. Companies hiring for bookkeeping jobs often offer remote, work-from-home, or hybrid work.
Common bookkeeping job titles include bookkeeper, controller, and billing specialist. Entry-level bookkeeping jobs are available, as well as manager and director-level roles for more experienced professionals. There are also opportunities for freelance, full-time, part-time, and flexible schedules. Whether you are looking for work from anywhere bookkeeping jobs or remote “bookkeeping jobs near me,” FlexJobs can help your search.
Looking for remote, part-time, or freelance bookkeeping jobs? FlexJobs can help.
- Remote Bookkeeping Jobs
- Part-Time Bookkeeping Jobs
- Freelance Bookkeeping Jobs
- Entry-Level Bookkeeping Jobs
Which Types of Jobs Are Related to Bookkeeping Jobs?
Common bookkeeping jobs include math & economics jobs, HR & recruiting jobs, medical billing jobs, and analyst jobs.
More Information About Bookkeeping Careers and Finding Remote Jobs:
10 Companies That Hire for Remote Bookkeeping Jobs
10 Flexible Jobs Where You Work Alone
Remote Bookkeeping Jobs are also known as:
- online bookkeeping jobs
- virtual bookkeeping jobs
- work from home bookkeeping jobs
- telecommuting bookkeeping jobs
Need a well-designed resume template for your next bookkeeping job?
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FeaturedDrive relationship-building across study teams and vendors, enabling bridges to ensure project deliverables are coordinated and met. Quickly identify potential sources of issues (e.g., with patient recruitment and retention, monitoring visit strategy...
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1 week agoLead statistical programming activities as product lead for full development project or groups of projects in Oncology Therapeutics. Comply with company, department and CDISC standards and processes, ensuring statistical programming innovations and...
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New! YesterdayDevelop and Manage the QMS strategy for the company. Develop and execute a robust quality management strategy aligned with the organization's overall objectives and business goals. Define quality policies, standards, and guidelines to ensure consistent...
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New! YesterdayWorking with a cross functional team to produce, qualify and close quality sales leads. Analyzing customer needs in support of current business objectives. Presenting and articulating advanced product features, benefits, and overall product solutions...
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New! 2 days agoFull ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance with the clinical monitoring plan. Conducts monitoring (pre-study, initiation, routine...
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FeaturedNew! 2 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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New! 2 days agoThe Site contract and Budget Specialist (Contracts Analyst) will be responsible for the commercial relationship with sites involved in clinical trials including work from contract and amendment language, budget negotiation within the established...
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FeaturedNew! 3 days agoProvide administrative and technical support to project teams including planning, organizing and coordinating responsibilities at a global level with supervision (as required) of the operational activities. You will assist with initial setup, ongoing...
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FeaturedNew! 3 days agoAs an Assistant CRA, you will perform remote site management and monitoring activities on assigned project(s) in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and PPD procedural documents by reviewing study data...
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FeaturedNew! 3 days agoProvides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides medical consultation to...
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New! 3 days agoLead the development and execution of strategies and tactical plans across the Hematology-Oncology Therapeutic Area globally, in both the US and EUR/International regions, in collaboration with cross-functional teams (i.e., Clinical Development...
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New! 4 days agoLead the planning, execution, and oversight of clinical research projects, including coordinating the activities of cross-functional teams, ensuring compliance with protocols and standard operating procedures, and monitoring progress against project...
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New! 6 days agoReviews and provides editorial feedback on all MSMR submissions spanning a wide variety of military-related health surveillance reports. MS in Epidemiology, Biostatistics, Environmental Health, or similar and 5+ years interpreting health analysis. Hybrid.
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FeaturedNew! 6 days agoFunction independently as a lead statistician with minimal oversight to deliver the project statistician tasks/responsibilities, including analysis database creation, statistical analyses, and creation of formatted statistical analysis tables and...
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1 week agoManages all clinical operational and quality aspects of allocated studies, involving moderate to high complexity, in compliance with ICH-GCP. In accordance with project specific requirements, may assume Lead CTM responsibilities on a global ...
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1 week agoReceive, triage, manage, and reconcile adverse event reports, including those reported in the scientific literature, in accordance with contractual and regulatory timelines. Manage adverse events and endpoints. Preparation of adverse event narratives.
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1 week agoAs a Clinical Trial Coordinator, you will provide technical support to the project team and will coordinate non-clinical responsibilities of project administration. Excellent English, French, and Dutch language skills. Good communication skills. Remote.
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1 week agoProvide support to Global/Regional Regulatory Lead(s) for assigned countries and studies and may on occasion be requested to function as Regional Regulatory Lead. Preparation of Investigational New Drug (IND) applications to national Regulatory Authority.
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1 week agoDesigning and leading research projects or tasks using qualitative and quantitative methods. Identifying, acquiring, and analyzing health, health sector, and related economic data from government and other sources to complete project tasks.
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Featured1 week agoThe Oversight AD.D.S. D is accountable for strategic indication or client-specific portfolio management within a Therapeutic Unit. Provides therapeutic expertise in project delivery execution, demonstrating the ability to react quickly and...
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Featured1 week agoMay manage staff, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, coaching and mentoring. Accountable for strategic portfolio management for our diagnostics...
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Featured1 week agoServe as a key BPS Subject Matter Expert (SME) by providing technical and strategic leadership for the development of biologics such as monoclonal antibodies. Provide technical sales support in partnership with our commercial team to help customers...
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9 days agoLead and own all in vitro and in vivo non-clinical toxicology activities (non-GLP & GLP) for BBOT's pipeline. Design and communicate customized toxicology strategies for each program. Currently, all programs are small molecules for oncology indications.
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10 days agoDevelop Standard Operating Procedures, source documents, and plans for integration and implementation of social science research projects into the health center. Assist with compilation and reporting of information for Institutional Review Boards...
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10 days agoBe responsible for managing A.S.projects from early Discovery through Clinical trial support. Strong project management, analytical, problem-solving, strategic and organizational skills. Utilize project management tools to plan, track, prioritize a...
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11 days agoWe have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients.We are excited to expand operations in Asia Pacific. Impact ...
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Featured11 days agoIdentify opportunities that result in the expansion of the local GP database which will increase the number of practices working with us to achieve our study targets. Identify opportunities to expand our access to patients and achieve AES study targets...
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Featured11 days agoResponsible for implementing a range of moderate to complex analyses in support of clinical non-interventional studies (NIS) using collected data, such as chart review and prospective studies. This individual will work independently to support the NIS...
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Featured12 days agoMonitors all safety variables (AE, laboratory abnormalities, changes in patient medical status, evaluation of prescribed concomitant medication for protocol restrictions, and un-blinding requests) of clinical studies.Provides medical review of events.
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12 days agoFull ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance with the clinical monitoring plan. Conducts monitoring (pre-study, initiation, routine...
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12 days agoDevelops and implements projects to effectively improve and streamline operations and functions of the department. Defines issue management and scope management strategy. Manages on-going consensus among project team and programmers.Develops and...
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12 days agoWorks with internal teams to progress quality issues in QMS. Tracks timeliness of cases in QMS. Supports teams in creation of CAPAs. Maintains strong working knowledge of QMS. Interacts with QA Lead Manager and above as required for quality issue case...
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12 days agoResponsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned.
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12 days agoOwns and provides leadership for all aspects of the appropriate proposal process (text, quote, budget, and/or response to Requests for Information [RFIs]) for assigned/accountable opportunities (inclusive of managing opportunities autonomously.)
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12 days agoResponsible for general maintenance and any required archival of documents produced by the study project teams within CPS. Organizing, gathering, scanning, and filing of all applicable documents into appropriate electronic and/or paper copy locations...
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Featured12 days agoEnsures tasks delegated to PVG are properly executed. Adheres to applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues. Adheres to client SOPs/directives and project specific WPDs for assigned...
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Featured12 days agoCollaborates with the Project Lead for the development of the Project Plan and to prepare or present at client meetings, including bid defense and kick-off meetings. Bachelor's degree or equivalent and relevant formal academic/vocational qualification...
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13 days agoFull ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out. A first stable experience as a CRA, within the pharmaceutical industry or a CRO. Strong IT skills. Remote.
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Featured13 days agoManages all clinical operational and quality aspects of allocated studies, involving moderate to high complexity, in compliance with ICH-GCP. In accordance with project-specific requirements, may assume Lead CTM responsibilities on a global or regional...
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13 days agoLiaises with monitor and investigative sites to resolve outstanding regulatory issues identified. Assists with the identification of potential investigators and development/distribution of initial protocol packets. University degree in life sciences...
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13 days agoThe Director, Clinical Program Management is responsible for working cross functionally to deliver and oversee clinical programs and associated outcomes across our journeys, which span family forming (pregnancy, fertility, surrogacy/adoption) and...
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13 days agoReview, draft, negotiate and track a variety of legal agreements including master services agreements, partnership agreements, subcontractor agreements, confidentiality agreements, steering board committee agreements, and other client contracts.
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Featured15 days agoReport to the Director, Regulatory Affairs, the Sr Manager will plan, coordinate, and provide Regulatory Services activities supporting Regulatory Chemistry, Manufacturing and Controls (CMC) aspects of customer projects in accordance with the Regulator...
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Featured15 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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15 days agoWe are seeking a Principal Biostatistician to lead large global or other major projects, analyze all parts of any clinical study, and provide planning on multiple clinical studies from multiple clients including tracking project activities and project...
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