Clinical Trial Manager Jobs - Remote Work From Home & Flexible
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26 days ago我ndependently serves asClinical TrialLead on complex studies, applying and providing guidance to clients and team members on best practices tailored to the applicable project, patient population, investigational product and client. Responsible for...
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Featured20 days agoAccording to the specific role, coordinates, oversees and completes functions on assignedtrialsactivities detailed on the task matrix. Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in system.
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26 days agoProactively identify risks and escalate to ProjectManagerand other appropriate functional leads. Develop and maintain project-specificclinicaloperations plans as required per project. Minimum of seven years relevantclinicalresearch experience in...
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30+ days agoTheClinical Trial Manager(CTM) in Real World Solutions is responsible for the operational oversight of all the milestones and activities assigned projects, including site management and monitoring activities. This includes remote site management...
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Featured17 days agoWork directly with the study teams: in the development ofclinicalresearch documents including research protocols, informed consent documents, case report forms, study team worksheets and other documents; to guide the preparation of regulatory agency...
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26 days agoServes as a financial member of the Project Team with the goal to contribute towards timely, efficient & accurate preparation and tracking of site payments. Reviews the financial section of theClinical TrialAgreement (CTA) in order to prepare the ...
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Featured27 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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18 days agoA Research ProjectManagermay also be assigned to oversee various operational and training aspects of the EPIC / OnCore application used by the Research Enterprise. The RPM will work closely and collaboratively with a variety of faculty and staff at...
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26 days agoThe Senior Investigator Grants Associate position is designed to provide grant administration processing and financial support to the Finance Team and applicable project teams. The position requires the candidate to be detail oriented, analytical...
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30+ days agoTheClinicalProjectManager(CPM) is responsible for the planning, implementation and conduct of single region or less complex,clinical trialsin Phase I-III. The CPM is accountable for the day-to-day operations ofclinical trialsincluding, but not...
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20 days agoServes as a financial member of the Project Team with the goal to contribute towards timely, efficient, and accurate preparation and tracking of site payments. Reviews the financial section of theClinical TrialAgreement (CTA) in order to prepare...
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30+ days agoServe as the primary contact forclinical trialsacross the ACO to ensure appropriate communications,trialmanagement, and meeting of timelines. Develop strong working relationships and maintain effective communication with study team members and key...
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New!TodayYou will lead a cross-functional team through the planning and execution ofclinical trialswhile adhering to budget, scope and timelines. You will also interface with departmental teams (clinical, divisional, and external) and act as liaison with...
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30+ days agoThe CRM in close collaboration with seniorclinicalresearch staff and faculty investigators, is responsible for managing significant aspects of up to 5 - 15 different Vascular and Cardiothoracic Surgery Researchclinicaland devicetrials.
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Featured18 days agoThe PL Is accountable for the overall delivery of the project (quality, time, cost) on behalf of the organization. Establishes and communicates customer expectations to the project team with minimal direction. Ensures that escalation pathways are...
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New!6 days agoTheClinicalStudyManagerleads assignedclinicalresearch study planning, execution and management. The StudyManageris specifically accountable for completing activities to ensure appropriate sponsor oversight of study sites in accordance with GCP...
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27 days ago我n this role, you'll partner closely withClinicalOperations and adjacent teams to develop and execute operational services that accelerate ourclinical trialroadmap. You'll be in charge of managing active and planned real world prospectiveclinical...
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30+ days agoSenior ProjectManager(SPM) is responsible for the overall coordination and management ofclinical trialsfrom start-up through closeout activities. Directs the technical, financial and operational aspects of the projects. Ensure project deliverables.
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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 devicetrials. Remote with as-needed travel.
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New!5 days agoResponsible for management of assignedclinicalstaff to ensure projects are appropriately resourced and employees are trained and meeting corporate and project objectives, timelines, deliverables and milestones. Lead, coach, and motivateClinical...
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New!6 days agoLead the execution of Site Start Up & Activation for assigned research projects in accordance with the Scope of Work and Project Plan. Work with Operations Leads to develop and maintainclinicalproject plans, including but not limited toClinical...
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10 days agoLeads the performance of the Local Study Team at country level. Ensuresclinicaland operational feasibility assessment of studies is performed to the highest quality. Coordinates the site selection process by identifying potential sites. Performs...
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Featured1 week ago监督供应商和承包商,以确保学习clinical trialsare executed with high quality and within timelines to meet budget parameters. Minimum of 5 years of relevantClinicalOperations experience including development ofclinical计划……
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New!2 days agoServe as the primary TMF contact for assigned studies.Ensure TMF is complete and inspection ready throughout study lifecycle and documents are filed contemporaneously.Develop and maintain study-specific work instructions, as needed.Review documents.
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10 days agoResponsible for the management and career development of ourClinicalResearch Associate (CRA) workforce, as well as supporting the development of departmental initiatives to strengthen the quality and productivity of GCM operations. Master's degree.
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30+ days agoAct as leadtrialBiostatistician to provide statistical support forclinicalstudies in the study design, analysis, interpretation, and publication ofclinicalstudies. Co-author protocols, statistical analysis plan, study reports, presentations, and...
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New!4 days agoAs a service, product, functional and/or therapeutic area Specialist acting as the primary Sponsor/Client project liaison and advocate is responsible to plan, execute, manage, and monitor complex, multinationalclinicalresearch project(s), for...
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30+ days agoConduct market research to identify key customer segments, Gather user input fromclinicalcasemanagerson existing solutions and future product roadmap, Conduct usability studies and gather user feedback. Develop product requirements and specifications,
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Featured2 weeks agoResponsible for executing disclosure and transparency activities as directed, including the redaction and anonymization ofclinical trialdocuments required for public disclosure in compliance with regulatory requirements and policy and processes.
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10 days agoThis position requires the ability to independently lead, manage, and motivate a team of CRAs (employee and/or consultant) to a standard consistent with company values and overall focus on quality. Specific focus will be to ensure the right resources...
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30+ days agoSite selection, pre-trialassessment, subject recruitment and retention planning, site initiation, monitoring and close-out. Partnering with the CTA, LTM and GTM to ensure overall site management while performingtrialrelated activities for assigned...
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30+ days agoDevelops study budget based onclinicalprotocol and fair market analysis. Develop cost per patient budgets and site contracts for our SponsoredClinical Trials. Create monthly financial reports of allclinical trials. Develop program andtrial...
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New!TodayManage sites through life oftrialand close-out, including, the implementation, coordination and conduct ofclinicalresearch activities in compliance with applicable Corporate and Divisional Policies and Procedures under supervision of theClinical...
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Featured8 days agoWorking with Research Leaders for preclinical/clinicalresearch activities and drive Evidence Generation Strategy. Develop study-related materials (e.g. protocol). Perform assigned sub-project tasks with cardiovascular groupclinicalstaff.
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30+ days agoContinuously assess project status, reassess and revise risks, oversee issue documentation and escalation, and ensure the project team and stakeholders remain informed of project status, risks, and issues throughout the project (including both periodic...
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10 days agoAccountable for the end to end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, sponsor's policies and procedures, quality standards and adverse event reporting requirements.
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26 days agoYou will monitor and own the progress ofclinicalstudies at investigative sites and ensure thatclinical研究进行,记录和报告/protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate...
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30+ days agoEstablish and coordinate all ongoing study management activities, such as leading the cross-functional study team to develop an overall study execution plan to deliver crucial study deliverables. Cultivate and maintain strong relationships. Review data.
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30+ days agoYou will monitor and own the progress ofclinicalstudies at investigative sites and ensure thatclinical研究进行,记录和报告/protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all...
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30+ days agoYou will be responsible for collection and transcription of research patient data and study related information into research records and assist with maintenance of study patient files. You will work with study monitors to process and collect data and...
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1 week agoAs expert for the simulation modeling tool(s), you will create training materials and provide trainings for team members and support other simulation modeling tool users as Power User. Identify and suggest possible improvements for CTS data analysis...
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30+ days agoAuthors routineclinicaland regulatory documents (e.g.,clinicalstudy protocols,clinicalstudy reports, and investigator's brochures, and sections of regulatory submissions) in partnership with cross-functional team with oversight. Supportsclinical...
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New!2 days agoAct as subject matter expert, mentor, coach and/or provide performance feedback tomanagerfor 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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3 weeks agoThe RegulatoryManager(RM)/Senior RegulatoryManager(SRM) provides regulatory strategy and development guidance for optimal conduct ofclinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures...
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10 days agoThe RegulatoryManager(RM) provides regulatory strategy and development guidance for optimal conduct ofclinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures, ensuring timely preparation of...
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25 days agoManages and Leads Global CTT (Clinical TrialTeam), supportsclinicalsupply planning, and manages external vendors. Initiates recruitment/retention and enrollment planning for protocols (globally). Responsible for creating and maintaining project...
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30+ days agoThe RegulatoryManager(RM)/Senior RegulatoryManager(SRM) provides regulatory strategy and development guidance for optimal conduct ofclinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures...
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Featured26 days agoThe Senior FinanceManagerleads the financial planning and analysis activities, as well as Accounting for Latin AmericaClinical TrialsDivision. This team member will work with the Latin America leadership to develop and implement strategies to drive...
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1 week agoServe as an initial point of contact for new studies; Process intake forms and unfunded agreements; Correspond with sponsors to obtaintrialinformation & required documents to initiate the activation process; Monitor the status of start-up timelines.
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18 days agoAs a ContractManager, you will review, draft, negotiate and track a variety of legal agreements including confidentiality agreements, master confidentiality agreements,clinicalstudy agreements and amendment agreements.. This is a remote opportunity...
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