Clinical Research Remote Jobs in Nevada (US)
This page tracks remote clinical research openings that are location-eligible for Nevada.
This page tracks remote clinical research openings that are location-eligible for Nevada.
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1,573
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$103,000 - $169,793
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• Support set up and execution of late phase clinical trials with a focus on data quality • Assist in authoring clinical protocols, Investigators Brochures and other regulatory documents ensuring consistency and clarity • Provide input into and implementation of data management plan, CRF design, and data review oversight • Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission • Assists the management of collaborators, consultants, and/or Clinical Research Organizations in completion of key projects • Anticipate and actively manage problems across a broad spectrum of cross-functional teams • Work cross-functionally within teams to ensure clinical strategy is translated into the development of the study concept document, study protocol and related documents • Support appropriate training, recruitment, and development requirements for matrix team resources.
Role Description Under the direct supervision of Vice President of Clinical Strategy, assists in coordinating and supporting all clinical strategy activities and projects in accordance with the established policies and standards as well as state and federal regulations including HIPAA. - Perform and assist in preparing for: - Managed Care Business Reviews by analyzing pharmacy claims data - Create and update cost grids using AWP, WAC and ASP for internal and external stakeholders - Monitor and create pipeline presentations with actionable recommendations - Budget and pipeline forecasting - Open Sales and Managed Care education - Pharmacists and nursing education - Enhanced clinical outreaches - Participates in real world research projects - Assist with compliance and accreditations - Other presentations and projects as necessary - Prepare and present at Professional Advisory Committee - Assists in creating Clinical Strategy - Assists in research and provide drug information as needed. - Assist in coordination of APPE and AE students: - Projects - Onboarding and ensure smooth transition. - Assists in Educational Accreditation (CAPE, ACPE, BRN etc). - Maintain clinical strategy related folders in TEAMs and SharePoint - Performs other duties and tasks as assigned. Qualifications - Doctor of Pharmacy (PharmD) degree from an ACPE-accredited school of pharmacy. - Licensure: Current, active and in good standing pharmacist license in the state of employment. - Must be proficient and efficient in independent remote work. Must have reliable internet and cell phone service. - Excellent communication, presentational and interpersonal skills. - Excellent clinical knowledge and analytic abilities. - Strong Microsoft Excel, PowerPoint and Word skills. Requirements - Current, active and in good standing pharmacist license in the state of employment. Preferred Skills - Knowledge of contemporary specialty pharmacy practice and healthcare requirements. - Strong clinical acumen in specialty pharmacy disease states (Immunology, MS, RA, Oncology, Rheum etc.). - Demonstrated organizational and leadership skills.
UnitedHealth Group is a healthcare and well-being company that’s dedicated to improving the health outcomes of millions around the world. We are comprised of
Role Description The Senior Clinical Pharmacist serves as a subject matter expert for the Part D Stars measures as well as other medication related issues including navigating the pharmacy benefit. This role will foster and manage relationships with internal and external partners to produce positive health outcomes and solid star performance for the plan. Work Schedule (40 hrs./week): - Monday – Friday 8am – 5pm local time with flexibility based on travel requirements - Local, state, and national travel up to 25% of the time based on business needs - Flexibility to telecommute from anywhere within the U.S. Primary Responsibilities: - Provide clinical pharmacy advice and guidance on quality of care programs including HEDIS and CMS Stars programs - Develop and train best practices to improve medication adherence and medication related measure gap closures - Interpret pharmacy programs to write clinical guidelines, job aids, and decision trees - Write and collaborate on member/provider collateral materials for pharmacy programs - Work on program implementation teams and contribute to business process design and systems set up, troubleshooting, and updates - Review programs for compliance with state, federal, and CMS regulations and recommend remediation - Monitor impending legislation for potential impact on current and future programs - Analyze data and prepare management summaries related to work stream results, performance management results, audit results, CMS reporting, and client reporting - Perform quality audits, determine performance gaps and root causes, prepare reports and collaborate on remediation - Examine, evaluate, and provide recommendations to evolve and enhance clinical pharmacy programs and best practices Qualifications - High School Diploma/GED - Current and unrestricted pharmacist licensure in State of residence - 5+ years of experience working as a Licensed Pharmacist within varied practice settings - 5+ years of experience and/or knowledge of Medicare Part D, Medicaid, and/or commercial - 1+ year of experience delivering presentations to large audiences - Intermediate level of proficiency with navigating MS Office and Windows-based environment - Ability to travel up to 25% of the time Preferred Qualifications - Doctor of Pharmacy (PharmD) - Residency and/or Board Certification (ie: BCPS, BCACP, BCGP) - Clinical quality experience (ie: HEDIS, Stars, NCQA) - Experience with Medicare Advantage - Experience working closely with and influencing providers - Experience teaching, training, and presenting accurate clinical information verbally to a variety of audiences Soft Skills - Excellent written, verbal and presentation skills Benefits - Comprehensive benefits package - Incentive and recognition programs - Equity stock purchase - 401k contribution (all benefits are subject to eligibility requirements) Compensation The hourly pay for this role will range from $112,700 to $193,000 per annum based on full-time employment. Pay is based on several factors including but not limited to local labor markets, education, work experience, certifications, etc. Application Deadline This will be posted for a minimum of 2 business days or until a sufficient candidate pool has been collected. Job posting may come down early due to volume of applicants.
Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
• Serves as a statistical department resource, mentors biostatisticians on job skills, and oversees or develops training plans or materials for Biostatistics associates. • Conducts training sessions, or otherwise trains new hires and enhance the skills of existing personnel. • Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high quality work. • Provides independent review of project work produced by other biostatisticians in the department. • Provides support across all statistical tasks during the lifecycle of the project, from protocol to CSR. • Prepares or oversees the preparation of Statistical Analysis Plans (SAPs), including development of well-presented mock-up displays for tables, listings, and figures. Collaborates with sponsor, if required. • May be responsible as Lead Biostatician for the statistical aspects of the protocol, generation of randomization schedule, and input to the clinical study report. • Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. • Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis. • Implements company objectives, and creates alternative solutions to address business and operational challenges. • As biostatistics representative on project teams, interfaces with other departmental project team representatives. • Preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others.
Title: Clinical Deployment Site Lead (VA EHRM) Location: Any Location / Remote Job Description: Job Family: Process and Operational Efficiency Job Qualifications: Skills: Collaboration, Information Systems, Leadership Certifications: None Experience: 5 + years of related experience US Citizenship Required: No Job Description: GDIT's Federal Health Division is hiring a Site Lead to provide operational leadership and coordination for a large-scale, multi-site Veterans Affairs Electronic Health Record (EHR) system deployment. - Work Location: Remote/Hybrid (Nationwide) - Travel Requirements: Up to 75% - Remote/Hybrid with extensive national travel This role is responsible for planning, executing, and managing of an assigned workstream across all phases of EHR deployment—pre-deployment, go-live, and post-deployment optimization. Acting as the primary point of contact for a workstream, the Site Lead ensures effective collaboration and communication among technical teams, clinical stakeholders, site leadership, vendors, and senior management. HOW YOU WILL MAKE AN IMPACT: - Lead and manage daily operational support for assigned EHR deployment workstreams. - Plan, track, and coordinate workstream activities to meet project goals, timelines, and budget constraints. - Serve as the primary liaison across technical, clinical, operational, and leadership stakeholders to promote effective decision-making and issue resolution. - Oversee all deployment phases, ensuring readiness, alignment, and seamless execution as sites transition to the new EHR. - Communicate routinely with stakeholders to provide updates, surface challenges, mitigate risks, and maintain progress on deliverables. - Build and maintain trusted relationships with client partners, vendor teams, and internal colleagues. - Develop deep expertise in the client’s policies, processes, workflows, and organizational structures to effectively carry out workstream responsibilities. - Support creation of program materials including data analysis, slide decks, written documentation, and status reports to inform leadership and drive progress. - Identify, document, and escalate patient safety concerns arising during deployment using established pathways for timely adjudication and resolution. - Coordinate triage activities related to incident management workflows, forums, and stakeholder events. - Provide onsite support as needed for readiness activities, go-live activation, and post-deployment optimization. - Ability to travel up to 75% to various VA client sites. nationwide. WHAT YOU'LL NEED (required): - Bachelor’s degree and 5+ years of progressive electronic health records (EHR) support outcome-based functional capability of an assigned workstream across any phase of EHR implementation - 3+ years of direct project management and stakeholder engagement experience supporting EHR activities for a software as a service (SaaS) managed EHR solution - Proven experience working in a clinical environment supporting project management - Strong organizational, communication, and problem-solving skills - Must be able to obtain a Position of Trust and successfully pass a thorough Government background screening process requiring the completion of detailed forms and fingerprinting WHAT WOULD BE EVEN BETTER (highly preferred): - Experience with Clinical Information Systems - Prior experience in Healthcare IT or EHR deployment environments - Demonstrated expertise in the relevant workstream domains supporting EHR deployments - Experience working within federal, veteran, or military healthcare environments - Familiarity with clinical workflows across inpatient and outpatient settings WHY GDIT: - Work on a mission that matters—delivering outcomes for Veterans and their families. - Access the latest cloud and automation technologies in a modern engineering environment. - Enjoy flexible work options, continuous learning, and a strong culture of purpose and performance. - Be part of a collaborative team driving innovation in government IT. #GDITFedHealthJobs #GDITHealth #VAeHRMsupport The likely salary range for this position is $124,093 - $144,900. This is not, however, a guarantee of compensation or salary. Rather, salary will be set based on experience, geographic location and possibly contractual requirements and could fall outside of this range. Scheduled Weekly Hours: 40 Travel Required: 50-75% Telecommuting Options: Remote Work Location: Any Location / Remote Total Rewards at GDIT: Our benefits package for all US-based employees includes a variety of medical plan options, some with Health Savings Accounts, dental plan options, a vision plan, and a 401(k) plan offering the ability to contribute both pre and post-tax dollars up to the IRS annual limits and receive a company match. To encourage work/life balance, GDIT offers employees full flex work weeks where possible and a variety of paid time off plans, including vacation, sick and personal time, holidays, paid parental, military, bereavement and jury duty leave. GDIT typically provides new employees with 15 days of paid leave per calendar year to be used for vacations, personal business, and illness and an additional 10 paid holidays per year. Paid leave and paid holidays are prorated based on the employee’s date of hire. The GDIT Paid Family Leave program provides a total of up to 160 hours of paid leave in a rolling 12 month period for eligible employees. To ensure our employees are able to protect their income, other offerings such as short and long-term disability benefits, life, accidental death and dismemberment, personal accident, critical illness and business travel and accident insurance are provided or available. We regularly review our Total Rewards package to ensure our offerings are competitive and reflect what our employees have told us they value most.
We’re Built for Biotech℠, dedicated to helping today’s top innovators turn big ideas into life-changing treatments.
Role Description Premier Research is looking for a Clinical Lead II (Oncology) to join our Clinical Management team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here. What You'll Be Doing: - Serves as initial point of contact for all site management and monitoring quality concerns, including initiation and oversight of site performance improvement plans (sPIP). - Plans, presents and participates in sponsor calls, representing Clinical and SSU function by providing status updates on clinical deliverables. - Oversees the quality of clinical monitoring, central monitoring and site management deliverables through the use of dashboards/reporting tools. Strong contributor to the central monitoring plan. - Monitors clinical operations metrics, activities and timelines on a regular basis; Tracks data entry timelines, open actions, protocol deviations, queries aging reports, SDR/SDV backlog and monitoring visit report turnaround timelines. - Ensures a state of audit readiness for both Premier and sites. Reviews/responds to audit findings and support sites in remediation/responses to any site audit findings. - Escalates through the established channels CRA/CM/SSU performance concerns, quality events, data breaches, serious breaches, scientific misconduct or any other event that requires prompt assessment and reporting. Qualifications - Bachelor’s degree, or its international equivalent from an accredited institution, in a clinical, biological, scientific, or health-related field; or equivalent work experience. - 2 years of experience as a Clinical Lead. Prior onsite monitoring experience including experience with Risk-Based Monitoring is preferred. - Required Therapeutic Area: Oncology. - Strong leadership skills including organizational skills, ability to persuade and motivate team members and sites to achieve targets. - Working knowledge of clinical financials including understanding of budgets, pass-through and resource management. - Ability to multitask and work effectively in a fast-paced environment with changing priorities. Requirements - Minimum base pay for this role is $116,000.00 USD. - Actual salary will be influenced based on a variety of factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. Benefits - Comprehensive benefits package, which may include health insurance, retirement plans, and paid time off. Company Description Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status.
Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
• Provides support across all assigned statistical tasks during the lifecycle of the project, from protocol to CSR. • Prepares Statistical Analysis Plans (SAPs), including development of well-presented mock-up displays for tables, listings, and figures. Collaborate with the sponsor, if required. • May be responsible for the statistical aspects of the protocol, generation of randomization schedule, publications and input to the clinical study report. • Coordinates the activities of other biostatistics and statistical programming personnel on assigned projects to ensure timely completion of high quality work. Provides independent review of project work produced by other biostatisticians in the department. • Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. • Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis. • Conducts and participates in verification and quality control of project deliverables, ensuring that output meets expectations and is consistent with analysis described in SAP and specifications. • Implements company objectives, and create alternative solutions to address business and operational challenges. • Serves as biostatistics representative on project teams, interfacing as necessary with other departmental project team representatives. This would include preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others. • Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, adapts to timeline or priority changes by reorganizing daily workload, and proactively communicates to biostatistics management any difficulties with meeting these timelines. • Monitors progress on study activities against agreed upon milestones and ensures the study
Role Description The Sr. Clinical Research Associate (Sr. CRA) is responsible for set-up, initiation, execution, monitoring, and close-out of IVD and medical device clinical trials at external clinical research sites and/or laboratories. The Sr. CRA should be able to independently train and manage external clinical research sites. This position reports to the Manager, Clinical Site Operations and is part of the Global Clinical Affairs organization. The position will be fully remote within the United States. In this role, you will have the opportunity to: - Oversee clinical study protocol execution at external sites, from start-up to close-out, ensuring timely data collection and compliance with FDA standards and Good Clinical Practice (GCP). - Develop and maintain relationships with institutions, study investigators, internal stakeholders, and vendors to ensure successful trial execution, data integrity, and adherence to project requirements. - Conduct independent study monitoring, including site coordination, investigational product accountability, and assessments of protocol deviations and/or adverse events, and drive clinical data quality which can include follow-up on incomplete data entry and/or outstanding queries. - Manage IRB submissions and all study regulatory documentation to ensure Trial Master File is kept up to date and audit ready. - Contribute to study planning including budget and contract negotiation and timeline forecasts, site identification and qualifications, and process improvement initiatives within the Global Clinical Affairs organization; as well as prepare study documents, including creating clinical templates, such as informed consent forms, clinical monitoring plan, etc. Qualifications - Bachelor’s degree with 5+ years clinical research experience OR Master’s degree with 3+ years clinical research experience OR Doctoral degree in field with clinical research experience. - Basic knowledge of regulatory requirements and Good Clinical Practice for in vitro diagnostic and medical device products. - Previous experience with managing clinical research sites and monitoring clinical study data. - Good technical background to understand and communicate current and new technologies. - Ability to work on multiple projects simultaneously. Requirements - Ability to travel 20-70%– including overnight(s), within the US. Travel may be up to 70% during project initiation periods. Benefits - Comprehensive package of benefits including paid time off, medical/dental/vision insurance, and 401(k) to eligible employees. - This position is eligible for a remote work arrangement in which you can work remotely from your home. - Annual salary range is $103,000.00 - $130,000.00. - This job is also eligible for bonus/incentive pay.
• Serves as the clinical trial lead responsible for the planning, conduct and oversight of the operational portion of clinical studies • Primary clinical point of contact with the client • Collaborate with PM on monthly invoicing and variance management of clinical budget • Develop study related clinical documents (e.g. clinical plans, Informed Consent Form templates, study specific forms and manuals, CRF completion guidelines, study trackers, PSV/SIV slides and other training materials) • Identify and develop training needs for CRAs and third-party vendors specific to the study, protocol and practices including presenting these at Investigator Meetings and Study Kick-off meetings • Generate potential site list from key stakeholders and drive site feasibility process • Identify potential risks to the enrollment targets based on feasibility analysis and site’s contracted commitment • Develop and finalize the country recruitment/retention strategy • Develop timely and effective communication and good working relationships with investigators and study team to ensure effective and timely feasibility, site start up, enrollment, maintenance and close out procedures • Lead internal clinical team meetings and sets expectations for clinical team of CRAs and CTAs • Address all CRA and site questions and maintains Frequently Asked Question (FAQ) log as appropriate • Support in planning and conducting investigator meetings • Review and/or approve of IP release packages • Oversee, support and track all submissions and approvals to Competent Authorities and IRB/Ethics Committees in conjunction with regulatory departments as applicable • Develop clinical monitoring strategies for assuring study timelines are met and assuring quality deliverables • Generate and utilizes metric reporting (e.g., CTMS, DM Query Trends, Outstanding Monitoring Reports) to ensure that the study is conducted per plan and communicates issues to PM and CRAs as appropriate • Responsible for eTMF implementation and management • Collaborate with PM, CRAs and QA to develop any Corrective and Preventative Action Plan (CAPA) and is accountable for implementation and timely closure • Accountable to assist sites, internal staff and CRAs with the preparation for GCP audits • Work closely with PM for project-specific resourcing issues • Escalate pertinent CRA performance and site compliance issues when necessary • Collaborate with data management and CRAs to ensure data quality and compliance with data cleaning timelines • Manage processes for investigational product (IP) including drug accountability and reconciliation • When a cross-functional PM is not assigned to a given program, the CTM will assume project management responsibility as needed • Support business development and marketing activities as appropriate • May negotiate site budget and investigator contract with support from the legal department and/or site contracts group • May review site visit reports and ensures monitoring (i.e. scheduling and scope) is executed per monitoring plan • May be responsible for management of clinical vendors (e.g. labs, IP, patient diary, home health care) in conjunction with PM • May perform clinical data review of patient profiles, data listings and summary tables, including query generation • May have line management responsibilities • Performs other duties as assigned by management
Precision Medicine Group delivers specialty services that help its life science clients navigate healthcare challenges. The company entered its 10th year of suc
Role Description Serves as the clinical trial lead responsible for the planning, conduct and oversight of the operational portion of clinical studies per defined scope of work and ensures that clinical studies are conducted in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP and all applicable regulatory requirements. - Primary clinical point of contact with the client - Collaborate with PM on monthly invoicing and variance management of clinical budget - Develop study related clinical documents (e.g. clinical plans, Informed Consent Form templates, study specific forms and manuals, CRF completion guidelines, study trackers, PSV/SIV slides and other training materials) - Identify and develop training needs for CRAs and third-party vendors specific to the study, protocol and practices including presenting these at Investigator Meetings and Study Kick-off meetings - Generate potential site list from key stakeholders and drive site feasibility process - Identify potential risks to the enrollment targets based on feasibility analysis and site’s contracted commitment - Develop and finalize the country recruitment/retention strategy - Develop timely and effective communication and good working relationships with investigators and study team to ensure effective and timely feasibility, site start up, enrollment, maintenance and close out procedures - Lead internal clinical team meetings and sets expectations for clinical team of CRAs and CTAs - Address all CRA and site questions and maintains Frequently Asked Question (FAQ) log as appropriate - Support in planning and conducting investigator meetings - Review and/or approve of IP release packages - Oversee, support and track all submissions and approvals to Competent Authorities and IRB/Ethics Committees in conjunction with regulatory departments as applicable - Develop clinical monitoring strategies for assuring study timelines are met and assuring quality deliverables - Generate and utilizes metric reporting (e.g., CTMS, DM Query Trends, Outstanding Monitoring Reports) to ensure that the study is conducted per plan and communicates issues to PM and CRAs as appropriate - Responsible for eTMF implementation and management - Collaborate with PM, CRAs and QA to develop any Corrective and Preventative Action Plan (CAPA) and is accountable for implementation and timely closure - Accountable to assist sites, internal staff and CRAs with the preparation for GCP audits - Work closely with PM for project-specific resourcing issues - Escalate pertinent CRA performance and site compliance issues when necessary - Collaborate with data management and CRAs to ensure data quality and compliance with data cleaning timelines - Manage processes for investigational product (IP) including drug accountability and reconciliation - When a cross-functional PM is not assigned to a given program, the CTM will assume project management responsibility as needed - Support business development and marketing activities as appropriate - May negotiate site budget and investigator contract with support from the legal department and/or site contracts group - May review site visit reports and ensures monitoring (i.e. scheduling and scope) is executed per monitoring plan - May be responsible for management of clinical vendors (e.g. labs, IP, patient diary, home health care) in conjunction with PM - May perform clinical data review of patient profiles, data listings and summary tables, including query generation - May have line management responsibilities - Performs other duties as assigned by management Qualifications - Minimum Required: Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred - Minimum of 7 years of clinical research experience or proven competencies for the position with significant clinical monitoring experience - Preferred: Advanced degree - Other Required: Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint) - Excellent communication and interpersonal skills to effectively interface with others in a team setting - Excellent organizational skills, attention to detail, and a customer service demeanor - Ability to travel domestically and internationally including overnight stays Requirements - Demonstrates mastery knowledge of ICH-GCP, relevant Precision SOPs, and regulatory guidance, as well as the ability to implement - Working knowledge of clinical management techniques and tools - Direct work experience in a cross-functional environment - Proven experience in functional management including proven experience in delegating while fostering cohesive team dynamics - Proven experience in planning, risk management and change management - High level of integrity and must inspire and demand the highest standards from a professional and ethical perspective - Ability to lead and inspire excellence within a team - Ability to create an environment where employees have a sense of ownership that will lead to increases in productivity and efficiency - Results oriented, accountable, motivated and flexible - Excellent time management, negotiation, critical thinking, decision making, analytical and interpersonal skills - Excellent presentation, verbal and written communications skills - In depth proven experience in pharmaceutical and/or device research required - Demonstrated successful independent negotiation and conflict management strategies Benefits - Compensation range: $110,700 — $200,900 USD - Discretionary annual bonus - Health insurance - Retirement savings benefits - Life insurance and disability benefits - Parental leave - Paid time off for sick leave and vacation
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