Analyst Jobs - Remote Work From Home & Flexible
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Dane N.
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Welcome to remote, part-time, freelance, and flexible analyst jobs! Analyst professionals take information (research) and discern its possible meanings and implications. Analyst professionals are employed in a wide range of industries, and the type of information being analyzed is dependent on the industry.... More
Welcome to remote, part-time, freelance, and flexible analyst jobs! Analyst professionals take information (research) and discern its possible meanings and implications. Analyst professionals are employed in a wide range of industries, and the type of information being analyzed is dependent on the industry. Companies hiring for analyst jobs often offer remote, work-from-home, or hybrid work.
Common analyst job titles include financial analyst, data analyst, and business analyst. Entry-level analyst 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 analyst jobs or remote “analyst jobs near me,” FlexJobs can help your search.
Looking for remote, part-time, or freelance analyst jobs? FlexJobs can help.
Which Types of Jobs Are Related to Analyst Jobs?
Common analyst jobs include big data jobs, internet research jobs, product owner jobs, and data scientist jobs.
More Information About Analyst Careers and Finding Remote Jobs:
10 Companies That Hire for Remote Business Analyst Jobs
What Is a Business Analyst? Job Description, Salary, and Skills
Remote Analyst Jobs are also known as:
- online analyst jobs
- virtual analyst jobs
- work from home analyst jobs
- telecommuting analyst jobs
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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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Featured12 days agoProvides leadership to direct reports by cultivating a supportive, motivating and collaborative work environment. Management responsibilities include onboarding, salary administration, performance management including promotion and discharge...
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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 agoDevelop and maintain comprehensive CP strategic development plans for assigned clinical development programs/studies. Provide CP subject matter expertise to the clinical study team/development team. Draft and finalize CP related report templates.
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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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2 weeks agoProvide comprehensive clinical and administrative support with protocol development review, regulatory review, and the implementation process as well as oversees medical writing/editing, regulatory/ compliance, and protocol coordination/navigation and...
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15 days agoThe Senior CTM will manage existing clinical projects and should have specialist knowledge of applicable regulations, nationally and internationally as appropriate. Advanced degree in a health-related field is preferred with 7+ years in clinical trials.
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Featured15 days agoMonitor, anticipate, pre-evaluate and communicate on pharmaceutical regulations impacting the Biological Drug Substance business: Lean in reputable industry trade association, influence on trends and provide SME consultation to organization.
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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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