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 —聘请了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 —聘请了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 —聘请了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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FeaturedNew!YesterdayProvide 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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New!YesterdayYou will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all...
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New!YesterdayDesign and implement relationship development and future sales planning within strategic accounts with focus on supporting current program development and repeat business from current biotech and pharmaceutical companies. Represent the company at...
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FeaturedNew!YesterdayResponsible for the management of designated clinical trials including investigator recruitment and selection, analysis of potential patient recruitment, preparation of trial related documentation (protocols, case report forms, investigators brochures...
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New!YesterdayClinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.
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New!YesterdayDelivery of innovative scientific and medical content (DSE/digital/MSL materials/FAQs/Medical Information Letters) tailored to specific audiences in the US and globally via impactful formats and relevant channels. High school diploma / GED & 12 years...
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New!2 days agoBuild and lead a group of PhD and non-PhD level scientists to conduct preclinical and translational drug development from candidate nomination to phase I, by developing a translational/biomarker plans, strategy and go/no go criteria at each stage of...
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FeaturedNew!2 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!2 days agoDevelop client focused budgets and proposals for the conduct of Phase I-IV clinical trials, including simple bid grid mapping with manager support. Work in collaboration with global operational review teams to develop high quality budgets and proposals...
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FeaturedNew!2 days agoThe Project Manager and Dashboard Lead arE accountable for the successful execution of all tasks related to the production of Real-World Data Solutions. This role is responsible for engagement with our clients and commercial sales teams from the...
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FeaturedNew!3 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!3 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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FeaturedNew!5 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!5 days agoSupports audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable...
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1 week agoServe as the designated radiation safety officer (RSO) for more than one medical facility. Responsible for overseeing that radiation safety surveys of radiation sources used within the facility are performed; monitors radiation exposure of workers.
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1 week agoDeveloping client-ready deliverables including protocols, statistical analysis plans, technical reports, and slides. Contributing to short-term resourcing discussions. Managing the delivery of components of projects by collaborating with other staff...
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8 days agoWork with brand teams to prepare and submit completed digital and print creatives for medical/legal/regulatory (MLR) submissions. Train and supervise junior staff members. Establish and cultivate relationships with MLR counterparts to discuss...
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8 days agoMonitor & manage all aspects of designated clinical trial protocols in Global Central Labs and is accountable for overall project performance and client's satisfaction by meeting their needs and expectations through the life cycle of the assigned trials.
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8 days agoWrite copy to the highest standard (quality and scientific) for a range of educational materials including the development of oral presentations, publications, print items, and digital platforms, and for different audiences. 1-3 years of experience.
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8 days agoYou will work with the Data Governance team to ensure that the Customer Success department and leadership have access to reliable and actionable data which will be used to build and monitor programs that improve our operational success and help...
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8 days agoYou will be responsible for ensuring successful delivery, user adoption, and outcomes of your assigned portfolio of clinical trials. You will plan, execute, and manage the implementation and usage of the product on clinical trials. You will have the...
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8 days agoThe Patient Partner Research Scientist reports directly to the Senior Director of PEI within the Patient-Centered Research Team. Be responsible for designing, leading, and delivering Evidera's patient engagement and patient-centricity advisory board...
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Featured8 days agoProvides administrative and technical support. Supports audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document. Aids the development of the critical path for site...
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9 days agoServe as clinical expert to provide clinical/scientific knowledge into the development, delivery and communication of the global scientific/medical evidence plan for the indication. Support cross-functional and global collaborations to integrate broad...
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9 days agoSeeking a Research Data Analyst to support research data collection, management, and analysis activities as part of a coordinating center for a consortium conducting clinical trials in the area of orthopedic trauma.
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9 days ago寻找一个老的研究总结m Coordinator II who will contribute to high-level special projects in support of a number of research efforts focused on the role of sleep, infections, health status, and mental health in cognitive decline and related...
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9 days agoAct in a liaison capacity between appropriate management personnel and staff, transmitting decisions and information to organizational units as appropriate, as well as outside agencies and organizations. Bachelor's degree in business, science, or...
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9 days agoCoordinate and manage all aspects of the registry build, including governance. Lead protocol development, consent and data capture and management activities. Development of recruitment, retention and engagement plans. Ensure that all outside vendor...
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Featured9 days agoThe Senior SAS Programmer 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 review and prospective studies. This individual will work...
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9 days agoServes as a regulatory compliance analyst, educator, and manager who exercises operational responsibility daily for the Institutional Review Board(s) to which they are assigned and charged with protecting the rights and welfare of human research...
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9 days agoProvides Medical and Safety monitoring on projects. Provides expert advice and detailed clinical development strategies for allocated project(s), including RFP/RFI, protocol development, study design, investigator brochure development, regulatory...
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Featured10天前Serves as a creator/contributor for signal detection and product safety scientist tasks which are ultra-high in complexity or which concern ultra-high complexity products, under supervision by a more experienced team member. Conducts quality review...
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10天前Oversees the large, complex, and highly diversified research portfolio including proposal development and post-award management. Oversees the submission of proposals from more than 20 faculty and researchers and over 35 sponsors, mainly federal and...
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10天前Assist in the processing of all research applications for all Campuses the IRB Committee reviews in accordance with the federal regulations. Assist in conducting preliminary reviews of all IRB applications to ensure compliance with policies.
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10天前Manages and drives all aspects of document development, revision, retirement, according to the Procedure section of this Charter, ensuring documents are written in alignment with sponsor procedures and quality standards. Ensures Document Owner is...
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10天前Consultant in HE/HTA statistics (+/-100% of the work): As a Statistician you will work directly with the HE team to produce high-quality statistical and economic statistical analysis and reporting. The intention is for the statistician to work...
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Featured12 days agoSet project goals and timetables, ensuring that all implementation and administrative activities are completed. Coordinate, plan and attend meetings; monitor activities to ensure objectives have been met within designated time frame, and coordinate...
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12 days agoEffectively plan and execute multiple Data Management projects simultaneously. Provide updates directly to senior stakeholders as requested by management. Serve as a subject matter expert. Participate in Business Development presentations and bid...
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13 days agoEnsure that research supports broader vision and commercial, product, and clinical strategy. Design, implement, and manage a portfolio of projects that cover cost outcomes, clinical outcomes, and discovery research. Communicate about study results...
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2 weeks agoProactive KOL / treatment centre mapping & planning according to the scientific strategic needs of the product or therapeutic area. Conduct drug administration (dosing and administration) readiness trainings upon request. Support post-marketing studies.
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2 weeks agoDemonstrate understanding of the pharmaceutical industry and medical affairs. Oversee and, if necessary, perform targeted literature reviews to identify and summarize model inputs and methodology used in previous health technology assessments. Perform...
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15 days agoEnsures that the conduct of clinical studies at sites is in accordance with the protocol/protocol amendments, Good Clinical Practice regulations, International Harmonization Guidelines, applicable company Standard Operating Procedures (SOPs), and all..
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15 days agoThe Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures...
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Featured15 days agoReceives, prepares and submits safety reports to applicable parties. Escalates to lead and/or line manager if any issues are encountered. Ensures reports are submitted in compliance with regulatory timelines and country legislation. Assists in...
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Featured15 days agoFunctions 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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15 days agoManaging compliance activities related to publication development and archival of all required documentation in internal repository (e.g. iEnvision). Coordinating contracting and budget management activities related to confidentiality and consultant...
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Featured15 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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Featured15 days ago为公关提供管理和技术支持oject 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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16 days agoSupport neurogenetic programs within Experimental Medicine as a primary early clinical lead. Help design and conduct early clinical studies, from natural history through treatment proof-of-mechanism clinical trials. Author translational and pre-...
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Featured16 days agoEstablishes and communicates customer expectations to the project team with minimal direction. Ensures that escalation pathways are adhered to internally and externally. Leads the cross-functional project team to meet or exceed deliverables. Manages...
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