Clinical Research Jobs - Remote Work From Home & Flexible
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30+ days agoThe CRM in close collaboration with seniorclinical researchstaff and faculty investigators, is responsible for managing significant aspects of up to 5 - 15 different Vascular and Cardiothoracic SurgeryResearch clinicaland device trials.
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13 days agoEnsure thatresearchsupports broader vision and commercial, product, andclinicalstrategy. Design, implement, and manage a portfolio of projects that cover cost outcomes,clinicaloutcomes, and discoveryresearch. Communicate about study results...
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30+ days agoWork closely with the SeniorClinicalTrial Manager to support all aspects ofclinicalstudies from initiation, planning, execution, maintenance, and close-out. Take a leadership role in the assigned site and study management activities, including ICFs...
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New!YesterdayClinical ResearchAssociates (CRAs) play a vital role in ensuring ourclinical researchprograms are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.
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30+ days agoThrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, challenging projects. Perform and coordinate all aspects of theclinicalmonitoring process. You shall also be qualified to conduct...
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FeaturedNew!3 days agoPerform and coordinate all aspects of theclinicalmonitoring 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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15 days agoTheClinical ResearchAssociate (CRA) will monitor the progress ofclinicalstudies at investigative sites or remotely, and ensureclinicaltrials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures...
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30+ days agoSite selection, pre-trial assessment, subject recruitment and retention planning, site initiation, monitoring and close-out. Partnering with the CTA, LTM and GTM to ensure overall site management while performing trial related activities for assigned...
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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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30+ days agoFull ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out. Planning and conducting various site visits (feasibility, site selection, interim and close-out) in...
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30+ days agoFull ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out. Planning and conducting various site visits (feasibility, site selection, interim and close-out) in...
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30+ days agoFunction in a lead role, meet with Vitalief'sclinical researchclient stakeholders to assess their currentclinicaltrials operational environment and understand what their business objectives are. Utilize business process improvement and change...
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15 days agoEnsures that the conduct ofclinicalstudies at sites is in accordance with the protocol/protocol amendments, GoodClinicalPractice regulations, International Harmonization Guidelines, applicable company Standard Operating Procedures (SOPs), and all..
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30+ days agoYou will monitor and own the progress ofclinicalstudies at investigative sites and ensure thatclinicalstudies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all...
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30+ days agoWork in multiple therapeutic areas to ensure compliance, data quality, monitor patient recruitment, and more. Must have a bachelor's degree and five years of direct experience. Full-time, remote job with travel. West coast applicants preferred.
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3 weeks agoSeeking a Legal Counsel to join its Global Regulatory Legal team to support continued growth of itsResearchContracts Center of Excellence, with a focus on pre-clinicalandclinical research, as well as specified corporate-level, cross-divisional...
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Featured30+ 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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30+ days agoPerform all type of visits from site feasibility to close out visits according to plan, document actions and follow up on action plans. Train and guide site staff in safety information handling, systems, protocol and trial procedures to minimize ...
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30+ days agoConfirms each project's scope in conjunction with the client and operational teams to ensure adherence to contractual scope, timelines and budget for all team members. Requires high-level skills in the areas of organization, multi-tasking...
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New!YesterdayYou will monitor and own the progress ofclinicalstudies at investigative sites and ensure thatclinicalstudies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all...
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30+ days agoAct as subject matter expert, mentor, coach and/or provide performance feedback to manager for peers. Assist with selection, hiring, training, and supervision of CRAs as needed. Perform co-monitoring and training visits with CRAs. When required, act...
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Featured30+ days agoApplies knowledge of scientific methods, including quantitative and qualitative with mastery of one area. Provides scientific leadership to OutcomesResearchteam members. Maintains line ofresearchand expertise in relevant scientific areas, along...
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9 days agoServe asclinicalexpert to provideclinical/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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30+ days agoAs a Principal working within a company at the forefront of digital innovation in the Life Sciences, you will help grow our practice in the US. Focus will be on building our brand in the market, developing our customer network and identifying and...
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25 days agoLead business development opportunities - identify and generate new project opportunities, clarify customers challenges and needs, be able to develop a compelling, differentiated proposal to solve these issues, and win new work.
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30+ days agoPrepare concise, well written, comprehensible technical reports and manuscripts describingresearchfindings for technical and general audiences, and for clients. Ph.D. degree with 0-3 years related experience or M.A., M.S., or M.P.H. or equivalent...
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9 days agoSeeking aResearchData Analyst to supportresearchdata collection, management, and analysis activities as part of a coordinating center for a consortium conductingclinicaltrials in the area of orthopedic trauma.
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30+ days agoPerform a variety of definedresearchand laboratory tests and experiments according to prescribed protocols and assigned schedules, set up experiments as prescribed by a principal investigator, and maintain record/logs of work performed.
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23 days agoAssist in preparation and reproduction of study materials during study start-up phase ofclinicaltrials. Follow up with outstanding documentations fromclinicalsites to complete site qualification. Schedule logistical and technical trainings with...
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18 days agoYou will directly manage scientists, external contractresearchlabs to supportclinicalvirology deliverables, including working cross functionally to meet timelines and budgets forclinicalvirology assays. Authorclinicalvirology reports,...
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30+ days agoTheClinicalData Coordinator will provide administrative, implementation processing and/or documentation support to multipleClinicalData Management project teams. Roles may include data entry, document/process/report development, and data/document...
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30+ days agoThrough the review of fertility medical records data, you will monitorclinicalcompliance with industry standards and record member outcomes to confirm they exceed industry standards supporting our members to achieve healthy birth outcomes. Bachelors.
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FeaturedNew!YesterdayResponsible for the management of designatedclinicaltrials 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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23 days agoConduct exploratoryresearch, concept validation and usability testing on various projects. Designresearchstudies, gather data, synthesize it into actionable insights and disseminate findings to various teams through reports and presentations.
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29 days agoThe SeniorResearchAssociate (SRA) based inClinicalOutcomes Assessment provides scientific leadership within project teams either independently and/or collaboratively withresearchscientists, in the conceptualization and execution of COA projects.
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30+ days agoResearch, develop and optimize advanced algorithms, actively engage and collaborate with the team and report results to a variety of audiences. Experience in C/C++ programming is needed. Option for remote job.
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30+ days agoDesign scientifically and strategically sound DMPK/ClinicalPharmacology studies. Analyze and summarize data and/or integrate study results into the ongoing development strategy. Write protocols and reports for nonclinical ADME andClinical...
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30+ days agoThis position will have oversight and responsibility for all EarlyClinicalDevelopment (ECD) functions: Manage a motivated group of physician-scientists engaged in the programs within the ECD portfolio. Author strategic content ofclinicaldevelopment...
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30+ days agoManage study operations including home-based assessments of cognitive function,clinicalassessments of neurological signs and symptoms, and hospital-based magnetic resonance imaging (MRI) studies of brain structure and function. Support quality...
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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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8 days agoSupports the VP in leading theclinicalgovernance for the KoothClinicalOperations function across North America. Work closely with senior staff in the service operations function to ensure that day-to-day management decisions are co-produced with...
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30+ days agoManage theclinicalintegrity of the assigned program and provideclinicalsupervision to therapists and case management staff. Will work in outpatient and field-based locations (clients' homes, schools, etc.) and in an office.
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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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30+ days agoSet project timelines, budget, necessary procedures, staffing requirements and resources in various phases of IVD projects. Must have a bachelor's degree, 4 years of PM experience, and 2 years in medical device trials. Remote with as-needed travel.
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30+ days agoThis person will use the PICOTS analytic framework to analyze published studies, assess strength of evidence (using the GRADE-based system), and write rapid and in-depth evidence assessments forclinicalevidence assessment membership services.
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30+ days agoLead ourresearchteam responsible for our delivering user insights across our product portfolio. Support and coachresearchersto collaborate effectively with cross-functional partners, translating their curiosities into actionableresearchquestions.
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25 days agoDrive and leadclinicaland perioperative consulting services, driving the programming, planning and design of healthcare facilities. Develop meaningful, long-term relationships with clients and internal partners through excellence, integrity...
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23 days agoContribute to program strategy, resourcing, budgeting, project plans, and oversight forclinicalstudies to achieveclinicalprogram goals.Lead the CRO/vendor selection strategy to support assigned studies, oversee the documentation for processes.
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Featured30+ days agoThe SeniorResearchScientist acts as an independent Principal Investigator for complex patient preference projects; expected to have comprehensive knowledge of best practices in patient preferenceresearchand understand how to apply these practices...
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26 days agoTheResearchData Coordinator II (RDC II) autonomously reviews and synthesize information from medical records (clinic notes, pathology reports, radiology reports, patient questionnaires, etc.) to extract industry, cooperative, and investigator...
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