2,267 Clinical Research jobs available for remote work from home. Apply for positions such as Medical Science Liaison (MSL), Clinical Research Associate I, Junior WordPress Developer (f/m/d), and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Medical Science Liaison is responsible for scientifically engaging with external stakeholders to address patient needs and improve medical outcomes. They also contribute to medical strategy, clinical trial support, and the gathering of medical intelligence to inform product development and launch roadmaps.
Conduct national monitoring across the UK for a diverse range of therapeutic areas including oncology and ophthalmology. Manage clinical trials using a risk-based monitoring model to ensure efficient trial oversight.
You will develop, maintain, and enhance WordPress websites using Elementor and Advanced Custom Fields while collaborating with designers to implement responsive layouts. Additionally, you will troubleshoot technical issues, ensure compliance with quality standards, and maintain documentation for development activities.
The Online Marketing Coordinator will support the planning and execution of digital marketing campaigns and create optimized content for various channels. They will also conduct market research, monitor campaign performance, and collaborate with internal teams to achieve business objectives.
The Contract Manager oversees the planning, drafting, and negotiation of clinical site contracts to ensure compliance with legal and regulatory requirements. They also provide functional line management to contract associates and serve as a key point of contact for clinical operations and legal teams.
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The Manager, Statistical Programming provides leadership and oversight for a global team, ensuring the delivery of high-quality clinical trial data products. They are responsible for managing project timelines, budgets, and resource allocation while fostering team development and process excellence.
Lead the enterprise data architecture strategy and design scalable, secure technology solutions across cloud, AI/ML, and data platforms. Partner with cross-functional teams to drive digital transformation and establish architectural standards for clinical research programs.
The Associate Director provides strategic leadership for protocol and site feasibility while overseeing the end-to-end lifecycle of clinical vendor partnerships. This role drives vendor selection, performance management, and cross-functional collaboration to ensure successful study execution and organizational growth.
The Senior Investigator Pricing Analyst will lead the development and maintenance of investigator grant forecasts by translating protocol assumptions into financial payment plans. They will partner with cross-functional teams to reconcile forecasts, identify financial risks, and implement standardized methodologies to ensure audit-ready financial reporting.
The Senior Medical Science Liaison drives high-impact scientific engagement and medical strategy execution within the diabetes care division. This role involves mentoring colleagues, managing complex initiatives, and fostering relationships with key thought leaders to advance organizational objectives.
Supports the Global Clinical Study Manager in the delivery of global clinical studies by ensuring quality standards, timelines, and budget adherence. Manages study-level documentation, system setups, and cross-functional team coordination to facilitate efficient clinical trial execution.
The Medical Science Liaison will develop and maintain scientific relationships with Key Opinion Leaders and provide clinical support for Cell Therapy Autoimmune products. They will also collaborate with internal teams to support clinical trial enrollment and provide scientific insights to stakeholders.
The Internal Auditor performs reviews of physician services medical records to ensure coding accuracy and documentation quality. They also identify coding trends, assess modifier assignments, and provide reporting for quality and statistical purposes.
The Medical Director is responsible for developing clinical research strategies and providing medical oversight for Phase 1-3 clinical studies. They will collaborate with cross-functional teams to ensure trial execution, safety assessment, and the development of clinical biomarker strategies.
The Sales Director will identify and close new business opportunities while managing the full sales cycle, including proposals, negotiations, and contract terms. They are also responsible for maintaining strategic account relationships and representing the company at industry conferences.
The Medical Science Liaison serves as a field-based medical expert responsible for communicating clinical and scientific data to healthcare stakeholders and decision-makers. They also provide pharmacoeconomic support to payers and IDNs while executing scientific engagement plans to advance corporate goals.
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The Patient Recruiter will conduct outreach to potential clinical trial participants and pre-screen them for eligibility based on study protocols. They are also responsible for maintaining accurate records in the CRM and collaborating with study teams to ensure timely enrollment.
The Regulatory Specialist will manage study start-up activities, including regulatory submissions and site credential management. They will also support the migration of regulatory data from Complion to Florence eRegulatory while ensuring all documentation is audit-ready.
The Director drives corporate policy development through strategic partnerships with government and industry groups to advance business objectives. They are responsible for monitoring federal legislation, influencing public policy, and representing the company before policymakers and trade associations.
The Scientific Advisor is responsible for developing high-quality scientific content and partnering with stakeholders to meet client strategy and branding objectives. They also collaborate with Client Services and Marketing teams to ensure project timelines are met and provide scientific expertise for clinical studies and product narratives.
The Clinical Research Associate will lead site start-up, activation, and investigator engagement for post-market safety studies and registries. They are responsible for conducting remote and on-site monitoring visits to ensure protocol compliance, data quality, and regulatory adherence.
The Feasibility Informatics Manager leads and manages clinical project feasibility processes to support proposal teams and business development. They act as a technical expert to provide strategic operational input and manage the delivery of awarded feasibility projects.
The Data Acquisition Specialist manages the definition, setup, and ingestion of external data streams for clinical trials. They liaise with stakeholders and data providers to ensure data transfer agreements are accurate and compliant with regulatory standards.
The Site Start-Up Specialist coordinates site start-up activities, manages essential regulatory documents, and ensures compliance with ICH/GCP guidelines. They serve as the primary contact for investigative sites and collaborate with stakeholders to ensure audit-ready documentation.
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The Marketing Specialist will manage trade show and event logistics while supporting the team with content creation, digital campaigns, and project coordination. They are responsible for maintaining brand guidelines, tracking deliverables, and assisting with various marketing initiatives to ensure project success.
The Director of Clinical Operations will lead cross-functional study execution teams and oversee the strategic and operational execution of clinical trials. They are responsible for managing trial budgets, selecting vendors, and ensuring compliance with regulatory standards throughout the drug development process.
You will lead statistical programming tasks, including developing and validating programs for clinical trial data analysis and reporting. Additionally, you will collaborate with biostatisticians to define analysis plans and ensure the accuracy of statistical outputs for regulatory submissions.
The Clinical Sales Specialist provides clinical and sales support by educating customers on Structural Heart products and providing technical assistance during procedures. They collaborate with Territory Managers to ensure optimal case coverage and clinical outcomes for patients.
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