Data Entry Jobs - Remote Work From Home & Flexible
I applied to over 130 jobs online (on other sites) and had given up trying. I honestly had no success despite having what I considered related experience, an accredited course, and a national certification exam. I only applied to approximately 10 to 12 jobs on FlexJobs. It is the best resource for flexible work. I've never been happier with my
career!
Jean B.
from
Jefferson Township, PA United States — Hired at Ciox Health as Coding Specialist
I found a job with FlexJobs in about two weeks. Even though it's not full-time salaried, it alleviated some financial hardship, and has helped me continue my job search without
stress.
Laurel S.
from
Germantown, MD United States — Hired at Rev as Transcriptionist
This was an incredibly helpful tool when I was looking for a legitimate telecommuting job in the coding field. I live in a rural town in eastern Oregon, and my profession isn't something that is in demand in this
area.
Kristen B.
from
Pilot Rock, OR United States — Hired at Change Healthcare as Coding Specialist
Welcome to remote, part-time, freelance, and flexible data entry jobs! Data entry professionals play an important role in organizations by ensuring the smooth and efficient processing of large amounts of information and data. Most data entry jobs include entering data into a computer system or a secure file system... More
Welcome to remote, part-time, freelance, and flexible data entry jobs! Data entry professionals play an important role in organizations by ensuring the smooth and efficient processing of large amounts of information and data. Most data entry jobs include entering data into a computer system or a secure file system and may include other types of clerical activities. Companies hiring for data entry jobs often offer remote, work-from-home, or hybrid work.
Common data entry job titles include data entry clerk, data entry specialist, and data entry manager. Entry-level data entry 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 data entry jobs or remote “data entry jobs near me,” FlexJobs can help your search.
Looking for remote, part-time, or freelance data entry jobs? FlexJobs can help.
- Remote Data Entry Jobs
- Part-Time Data Entry Jobs
- Freelance Data Entry Jobs
- Entry-Level Data Entry Jobs
Which Types of Jobs Are Related to Data Entry Jobs?
Common data entry jobs include typing jobs, transcription jobs, billing jobs, and virtual assistant jobs.
More Information About Data Entry Careers and Finding Remote Jobs:
What Are Data Entry Jobs? A Guide to Salary, Skills and Job Hunting
12 Companies That Hire for Remote Data Entry Jobs
Remote Data Entry Jobs are also known as:
- online data entry jobs
- virtual data entry jobs
- work from home data entry jobs
- telecommuting data entry jobs
Need a well-designed resume template for your next data entry job?
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New! YesterdayLeads the development of clinical program enhancements and better practices. Assists with development, enhancement, and maintenance of operational functions, policy and clinical support and provider education. Develops, implements, and monitors project...
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New! YesterdayLead the development and implementation of clinical specialty programs. Serve as a clinical liaison for assigned contract(s) and manage overall client relationship. Develop and track appropriate metrics to monitor quality and care cost impact of...
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New! YesterdayLeads clinical program enhancements, assists with operational functions, policy and clinical support, provider education, and oversees implementation of new specialty programs. Serves as liaison between company and customers.
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New! YesterdayLeads clinical program development, enhances operations, coordinates new specialty programs, resolves customer issues, manages complex projects, and integrates clinical programs with company initiatives. Play a role in various multi-functional projects.
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New! YesterdayOversee a complex portfolio of sponsored and non-sponsored research funding. Provide direct support to faculty and administrators with proposal preparation, budget development, and financial analysis. Ensure compliance with regulations and policies.
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New! YesterdayPartner with stakeholders to define project scope, goals, and tactics. Evaluate and document workflows, develop report formats, and oversee report development. Estimate project ROI and develop project communication plans.
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New! YesterdayLead LGBTQIA+/sexual and gender minority research program. Manage daily research-related components, supervise and coordinate clinical research staff, manage research operations, oversee execution of all aspects of research process and participate in ..
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FeaturedNew! YesterdayManages staff, conducts performance appraisals and career discussions, recruits and selects staff, delivers training, ensures adherence to ethical and regulatory standards, evaluates employee and project metrics, participates in process improvement...
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FeaturedNew! YesterdayManage clinical operations and quality aspects of studies. Develop monitoring strategy and clinical tools in alignment with study protocol. Collaborate with project lead and manage project financials. Responsible for the implementation and training of...
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FeaturedNew! YesterdayManages clinical operations, quality, finances, team, and project processes for Neurosciences studies. Collaborates with project lead, ensures timely deliverables, and assesses site feasibility. Relevant experience required.
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FeaturedNew! YesterdayManages clinical operations, quality, finances, and team for assigned studies. Develops monitoring strategy, ensures deliverables, and implements project processes. Collaborates with Project Lead and start-up team.
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FeaturedNew! YesterdayImplement, coordinate and facilitate study development of Reading Center projects. Oversee study and regulatory operations related to startup, maintenance and closeout for multiple multi-center, international clinical research studies. Devise and impl..
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New! YesterdayLead global biosimilar development, oversee cross-functional trial activities, ensure implementation of trials in accordance with guidelines, execute clinical studies with high quality, contribute to study document authoring and review.
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New! YesterdayDesign and analyze studies related to healthcare industry research. Develop and implement statistical methods and algorithms for analyzing data. Collaborate with researchers and healthcare professionals to determine study objectives, data collection m..
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New! YesterdayAssist in the creation and submission of regulatory documents, review regional component of the Global Regulatory Plan, and ensure compliance with submissions to regulatory agencies. Provide regulatory support to cross-functional teams and participate..
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New! YesterdayRetrieve, organize, validate, and deliver data to support research study protocols. Analyze qualitative and quantitative data from multiple sources and synthesize results into meaningful reports and presentations. Develop subject matter expertise arou..
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New! 2 days agoMonitor investigational sites, ensure data integrity and patient safety, execute on-site visits, manage trial master files, validate site documents, communicate with study teams. 3+ years monitoring experience and understanding of FDA and ICH/GCP regu..
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New! 2 days agoManage vendor category needs, assess new vendors and services, establish and maintain relationships with vendors, and analyze metrics to recommend best fit for a study. Requires experience in project trial delivery and CRO experience.
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New! 2 days agoManage all laboratory aspects of clinical trial projects, including study setup and planning, study activity monitoring and closeout, proactive communication with customers, and participation in meetings and training activities.
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New! 2 days agoManage laboratory aspects of clinical trial projects for a customer or program. Act as main point of contact for customers throughout study lifecycle, facilitate study set-up and planning, monitor study activity and closeout, and establish proactive l..
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New! 2 days agoLead drug substance process development and manufacturing, mentor team, manage financials, forecast expenditures, provide strategic input for regulatory filings. PhD in chemistry with 15+ years of technical and management experience required.
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New! 2 days agoLead analytical research and development and quality control activities for active pharmaceutical ingredients and drug products. Oversee release stability testing and analytical regulatory documentation to support global clinical studies. Mentor team ..
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New! 2 days agoDesign and implement drug product development strategies, manage budgets and financials, mentor and guide team members, author and review regulatory filings and technical documents, and lead cross-functional efforts to meet internal customer requirements.
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FeaturedNew! 2 days agoLead the cross-functional project team to ensure successful delivery of clinical trials in respiratory diseases. Manage project(s) of increasing complexity, establish and communicate customer expectations, and ensure compliance with policies...
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FeaturedNew! 2 days agoAccountable for project delivery, managing cross-functional teams, meeting customer expectations, and resolving issues. Requires therapeutic area knowledge, leadership, communication skills, and ability to manage complex situations.
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New! 3 days agoProvide grant development support and advice to faculty. Coordinate teams for complex grant proposals. Liaise with funding agencies. Identify funding opportunities. Write high-quality drafts of non-technical proposal components.Format proposal documents.
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New! 3 days agoEnsure institutional compliance in areas of human, animal, and stem cell research. Lead a team of 45 FTEs and provide guidance to faculty, researchers, and staff involved in research. Advise on regulatory matters and oversee policy development.
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New! 3 days agoManage all laboratory aspects of assigned clinical trial projects for a customer or specific program. Act as main point of contact for the customer throughout the study lifecycle. Facilitate study setup, monitoring, and closeout. Build and maintain...
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New! 3 days agoManage all laboratory aspects of assigned clinical trial projects, including study setup and planning, study activity monitoring and closeout, and proactive lines of communication. Represent the company at meetings and training activities. Assist in t..
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New! 3 days agoCoordinate, prioritize, and oversee administrative activities, finances, and communications for a public health research center. Develop and implement research projects, manage data, and supervise staff. Must have excellent organizational, communicati..
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New! 3 days agoSupport the development of clinical strategy for regulatory approvals and expanded indications. Prepare protocols and other relevant documents. Provide scientific expertise and build relationships with internal and external parties.
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New! 3 days agoContribute to clinical science activities, including protocol development, study implementation, data analysis, and reporting. Build relationships and assist with regulatory submissions. Minimum 7 years clinical study design experience required.
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New! 3 days agoDrive new business and develop client relationships in clinical research. Lead a business development team, communicate with stakeholders, execute account planning, meet revenue targets, and represent the company at industry events.
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New! 3 days agoDevelop clinical strategy, author protocols and scientific publications, provide scientific expertise to clinical trial managers, build relationships with internal and external parties, and analyze study data. Minimum 7 years of clinical study design...
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New! 3 days agoSupport the development of clinical strategy for regulatory approvals and expanded indications. Prepare scientific publications and presentations. Build and maintain relationships with internal and external parties. Assist with data collection...
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New! 3 days agoManage study tasks related to IRBs and study sponsors, resolve regulatory and sponsor-related issues, maintain study records, ensure compliance with regulatory guidelines, and communicate with sponsors. Bachelor's degree and 2 years of relevant resear..
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New! 3 days agoResearch Nurse I is responsible for providing patient care, educating patients and families, assisting with research operations, ensuring ethics and participant safety, managing data and informatics, and supporting site and study management.
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New! 3 days agoSupport clinical strategy development for regulatory approvals and expanded indications. Prepare protocols, author scientific documents, provide scientific expertise, build relationships, analyze study data, and author clinical documents for regulator..
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New! 3 days agoContribute to clinical science for regulatory approval, engage with physicians and payers, develop protocols, implement studies, analyze data, report results, build relationships, understand clinical landscape and future implications.
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New! 3 days agoMonitor clinical trial activities in compliance with regulations and guidelines, support project teams, identify and resolve issues, manage data and execute site close-out activities. Minimum 2 years of monitoring experience required.
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New! 3 days agoCoordinate and review clinical research-related charges, ensuring accuracy and completeness. Provide specialized support to clinical research staff and research finance. Utilize electronic platforms to review charges and direct them to appropriate cli..
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New! 3 days agoClinical Research Medical Director in Thoracic Oncology to provide clinical/scientific knowledge for global scientific/medical evidence plan. Serve as medical monitor on lung oncology trials. Support cross-functional collaborations for development pro..
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New! 3 days agoLead, manage, and coordinate clinical trials from start-up to close-out at a country level. Collaborate with cross-functional teams, oversee vendor activities, and ensure timely delivery of results within the local country.
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New! 4 days agoContribute to a research project studying diagnostic testing and treatment of acute disease among patients with Alzheimer's Disease. Use statistical software to work with large data sets, analyze data, conduct literature reviews, and draft reports and..
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New! 4 days agoPerform pre and/or post-award functions, coordinate institutional reviews and approvals, prepare financial transactions and reports, and troubleshoot and resolve matters related to sponsored funds and projects. Assist in the review of financial reports...
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New! 4 days agoReviews and ensures compliance of plain language summaries of clinical trial results. Assists in vendor oversight, provides feedback, and facilitates cross-functional discussions. Translates scientific content into easy-to-understand terms and applies..
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New! 5 days agoLead design, development, and implementation of customer-driven research on our Platform and Healthcare Member Systems. Collaborate with clients to fulfill research needs. Analyze Electronic Health Record data and respond to regulatory requests.
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New! 5 days agoSupport clinical trial activities including data monitoring, biobanking, and site visits. Manage supply orders and assist in audit readiness. Bachelor's degree and 5+ years' work experience in clinical field required. Travel up to 50%.
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New! 5 days agoDevelop and execute marketing strategies for a product area, coordinate with global counterparts, provide customer insights, support competitive analyses. 25% travel. 4+ years marketing experience required. MBA and medical device marketing preferred.
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New! 5 days agoOversee and develop clinical research studies, including study design and protocol development. Manage clinical study operations, budgets, and timelines. Build relationships and collaborations with internal and external stakeholders.
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