Medical Research Jobs - Remote Work From Home & Flexible
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 mysearch.
David B. from Kansas City, MO United States —Hired at Included Health as Engineering Manager, Infrastructure
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 everyday.
Art M. from Montgomery, AL United States —Hired at Ontrak, Inc. as Care Coach
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 mycareer!
Jean B. from Jefferson Township, PA United States —Hired at Ciox Health as Coding Specialist
Welcome to remote, part-time, freelance, and flexible Medical Research jobs!Medical research jobs are dedicated to aiding and supporting expanding knowledge in the field of medicine. Medical research focuses on new treatments and other research that leads to the development of new treatments for medical issues. From...More
Welcome to remote, part-time, freelance, and flexible Medical Research jobs!Medical research jobs are dedicated to aiding and supporting expanding knowledge in the field of medicine. Medical research focuses on new treatments and other research that leads to the development of new treatments for medical issues. From developing vaccines, antibiotics, and other medicines, to a greater understanding of health and disease; medical research offers a great variety of interest areas. People interested in medical research jobs would have a strong background in biomedical science, biology, chemistry, or physics. Medical researchers will primarily work with universities, federal governments, and within privately funded laboratories. If you are looking for medical research jobs, check out popular titles such as: clinical research associate, medical research assistant, and research laboratory technician. If you are passionate about expanding the field of medicine, a flexible position in medical research could be a great fit for your career. See below for the latest flexible and remote medical research jobs!
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New!YesterdayManage a portfolio of clinical research sites to drive adoption, retention and stellar customer satisfaction, and ultimately help our sites be more successful at recruiting & enrolling patients for clinical trials. Introduce, onboard and build ongoing...
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New!YesterdayWork with supervisor and various internal/external key stakeholders to resolve/escalate contractual issues. 1 year experience or equivalent working on budget development for France. Fluency in French and English is required. Ensure adherence to company...
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New!2 days agoAgreements, Amendments to Clinical Trial Agreements, vendor contracts and site budgets. Work with supervisor and various internal/external stakeholders to resolve contractual issues. Update relevant study team members regarding the status of contract...
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New!2 days agoResponsible for clinical account managers (CAM) performance and deliverables to our clients and key stakeholders (i.e. client success). Key deliverables to clients include drug trend reporting, cost savings initiatives, and clinical and operational...
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New!2 days agoAccountable for strategy, planning, definition of content, preparation, review, and approval of global regulatory CMC submissions and responses to Health Authority questions. Submissions must be in line with agreed global regulatory strategy and within...
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New!2 days agoResponsible for leading investigational drug services. In addition to managing various drug studies, this individual will work with the team to standardize processes and drive operational efficiency for research activities within Pharmacy Services.
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New!3 days agoWrite and update medical-related content topics in several formats for point-of-care and education products. Perform structured medical/nursing literature searches and research analysis to ensure inclusion of most recent evidence and guidelines in topics.
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FeaturedNew!3 days agoDelivers patient advisory board, patient insights and patient-centric trial strategy projects both independently and collaboratively as the lead or member of scientific project teams. This position is responsible for designing as well as leading the...
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New!3 days agoCoordinates, plans, organizes and oversees, in her regional location, the completion of administrative and technical tasks during the Dx study life time in collaboration with the Principal Investigator, the regional laboratory testing site and the...
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New!3 days agoOnboard the users with an initial phone call and complete a multidimensional assessment to gather relevant behavioral health history and symptoms. Monitor the progress of members and offer therapeutic strategies on how to deal with temptations and...
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FeaturedNew!4 days agoPerform and coordinate all aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently.Conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documents.
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FeaturedNew!4 days agoMonitoring independently different sites, including RBM - Participation in investigator meeting as necessary - Ensuring the trial is conducted in accordance with the approved protocol ICH-GCP guidelines, SOPs etc - Ensuring effective communication...
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New!4 days agoYou will lead the development and implementation of research initiatives, outcomes measurement, and quality improvement strategies to enhance the effectiveness and efficiency of our treatment programs. Background in research design, data analysis, and...
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New!4 days agoThe Senior Research Associate (SRA) based in Clinical Outcomes Assessment provides scientific leadership within project teams either independently and/or collaboratively with research scientists, in the conceptualization and execution of COA projects.
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New!4 days agoLeverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports. Build relationships. Oversee integrity of the...
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New!4 days ago数据管理器负责数据管理t activities for research studies. The data manager works as an integral part of a cross-functional team through the lifecycle of the research study from design through final analysis and study closeout.
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FeaturedNew!4 days agoProvide scientific guidance/consultation on methodological and operational considerations of study design and conduct. Lead or oversee the development of draft scientific project deliverables (e.g., protocols, case report forms (electronic or paper)...
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FeaturedNew!4 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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FeaturedNew!4 days ago设计一个科学负责人选d 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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FeaturedNew!4 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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FeaturedNew!4 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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FeaturedNew!4 days ago为全球提供监管文档支持Regulatory Affairs team members for Product Registrations, Renewals, Launches, etc. Provide support and needed information to all global regions on all US products across the product portfolio so that...
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FeaturedNew!5 days agoApplies relevant components of the project protocol to daily tasks and directs others on how to apply to their daily tasks. Acts as a liaison to the PM and/or client as required and communicates with management regarding all data management (DM)...
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FeaturedNew!5 days agoUtilize your project management skill set and medical terminology knowledge to understand our business and support impactful projects. Gain exposure through networking events and shadowing opportunities. Participate in professional development...
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New!5 days agoWe are looking for an occupational therapist, certified in lymphedema treatment, to serve as a lymphedema educator for a pilot lymphedema screening program at BMC. The job requires 4-6 hours of telemedicine visits a week with postoperative breast...
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New!5 days agoThe Director of Sponsored Programs Administration will lead pre-and post-award (non-financial) administration of sponsored programs, thus assuring a high quality, effective and efficient support platform for the research community. This position is...
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New!6 days agoThe Regional Study Coordinator II coordinates, plans, organizes, and oversees, in his regional location, the completion of administrative and technical tasks during the Dx study life time in collaboration with the Principal Investigator, the regional...
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New!6 days agoGive feedback on new and existing technologies for perioperative infection control. This includes being current on key publications - both scientific peer-reviewed and industry generated. Align & Coordinate Activities with both Corporate and Field...
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New!6 days agoResponsible for the operational planning, feasibility, execution and conduct of clinical trial(s). Serve as the Clinical Trial Team lead Leads and directs teams in key study planning, development, and execution elements (e.g. operational reviews...
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New!6 days agoDesign and maintenance of statistical databases that support multiple stakeholder groups which include clinical development, outcomes research and safety evaluation. Key collaborator with statistics and other project stakeholders in ensuring that...
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New!6 days agoDevelop, review, document and perform validation of SAS programs and macros. Support the development of data repositories, pooling multiple studies. Create standard reports in different output formats. Automate programming tasks within the SAS...
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New!6 days agoThe Senior Site Contract Analyst - Oncology will be responsible for the commercial relationship with clinical sites involved in clinical trials including work from clinical contract and amendment language, clinical budget negotiations within the...
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New!6 days agoBe responsible for supporting oversight of clinical specimens and associated laboratory data collected throughout the life of a clinical trial, including safety labs, PK, biomarkers, tumor samples, etc. and will assist in departmental infrastructure...
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New!6 days agoProvide Standard Analytical Product Package E2E services with regards to feasibility as part of the End to End Process (E2E) within Global Development, aligned with the program level strategy within the agreed timelines and at the highest quality...
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New!6 days agoIn this position, you will coordinate timelines and activities for biomarker projects to ensure high quality and timely delivery of biomarker results and maintain close contact with the Biomarker and Imaging program leadership to communicate activities.
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New!6 days agoManage clinical supply planning and forecasting for study protocols. Serve as member of clinical study team and/or clinical drug supply team, as assigned. Interpret relevant protocol information to develop packaging/labeling design and/or global...
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FeaturedNew!6 days agoProvide scientific guidance/consultation on methodological & operational considerations of study design and conduct. Lead or oversee the development of draft scientific project deliverables (e.g., protocols, case report forms), statistical analysis plans.
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New!6 days agoThe Central Services Specialist - ICF Management position will be responsible for review, coordination and finalization of Global Informed Consent Form templates for all clinical studies that are managed by Development Operations. Responsibilities also...
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FeaturedNew!6 days agoProvides scientific leadership to patient preference 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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FeaturedNew!6 days agoApplies knowledge of scientific methods, including quantitative and qualitative with mastery of one area. Provides scientific leadership to Outcomes Research team members. Maintains line of research and expertise in relevant scientific areas, along...
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FeaturedNew!6 days agoCompletes study and site management activities as defined in task matrix, and as applicable and directed for study assigned. Completes and documents study-specific training. Orients and trains on any company/study-specific systems. Provides in-house...
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1 week agoProvide senior leadership to the research portfolio to deliver timely, high-quality, and policy-relevant results as part of an ongoing production process for key indicators central to IHME's mission. Make strategic planning recommendations.
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Featured1 week agoPerform department, Internal, Country and Investigator file reviews as assigned, and documents findings in appropriate system(s). Ensure allocated tasks are performed on time, within budget and to a high-quality standard. Proactively communicates any...
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1 week agoCompletes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study...
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Featured8 days agoDevelop attractive customer propositions across the range of Clinical Services based on their current and future needs as uncovered during the sales process. Close and win business from both existing and new customers and business segments.
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Featured8 days agoThe successful candidate will primarily focus on the design, development, and maintenance of automated analytical and reporting pipelines. Master's degree and 5 years of relevant experience in large-scale, multi-source data collection, and analysis.
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9 days agoStudy concept development and execution of natural history of disease assessment for business and development and early development indications. Assess real world data assets and establish real world data plan, including data licenses and data platforms.
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10 days agoCoordinate activities related to enterprise medical and safety governance, serve as the Secretariat of Global Safety Committee, including managing agenda, issue meeting minutes and follow-up on action items.Drive and coordinate cross-functional...
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11 days ago坐标pre-award帮助等功能Principal Investigators in completion of grant proposals including budget development, drafting administrative sections, collecting materials, and obtaining institutional review/approval.
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12 days agoResponsible for the day-to-day operations and administration of the Patient Registry, working closely with our vendor. Supervise daily performance of Navigators and monitor quality of services provided; institute coaching to make improvements through...
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