2,591 Clinical Research jobs available for remote work from home. Apply for positions such as Senior CRM Business Analyst, In-House Clinical Research Associate I, Sponsor-Dedicated (Contract), In-House Clinical Research Associate I - Romania/Spain/Poland, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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Lead client workshops and discovery sessions to analyze business needs and recommend industry best practices for CRM and Speaker Bureau implementations. Partner with cross-functional teams to translate business requirements into functional specifications and support the full deployment lifecycle.
The In-House Clinical Research Associate will support clinical trial operations through remote monitoring, site support, and ensuring compliance with protocols and regulations. They are responsible for reporting serious adverse events and assisting with audit readiness and study start-up activities.
The In-House Clinical Research Associate will ensure the quality and timely submission of site data and manage regulatory and ethical documentation. They will also provide updates for the Trial Master File and conduct feasibility studies for potential clinical trial sites.
You will coordinate clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. This includes conducting site visits, verifying data accuracy, and managing documentation to guarantee subject rights and data reliability.
The Vice President of Sales is responsible for driving revenue growth through new business development and expanding services within large hospitals and health systems. This role involves managing the full sales cycle, from prospecting and cold calling to conducting value-driven presentations and maintaining executive-level client relationships.
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Conduct site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance, data integrity, and patient safety. Collaborate with investigators and site staff, review clinical data and resolve queries, and contribute to the preparation and review of study documentation.
The Medical Science Liaison is responsible for developing professional relationships with healthcare providers and delivering objective, non-promotional scientific information in the oncology therapeutic area. They also drive high-quality scientific exchange, generate actionable insights, and support clinical research initiatives while maintaining scientific integrity.
The OnCore Calendar Analyst is responsible for building and configuring study calendars within the Clinical Trial Management System (CTMS) based on research protocols. They also perform quality assurance, troubleshoot system issues, and provide technical support to research teams to ensure compliance with institutional standards.
The Project Manager oversees the initiation, planning, and execution of clinical research projects while managing study-specific vendors throughout the project lifecycle. They act as the primary contact for sponsors and internal teams to ensure project deliverables meet budget, scope, and regulatory requirements.
The Senior Clinical Research Associate will oversee clinical trial monitoring activities, ensuring compliance with GCP, local laws, and study protocols. They will serve as the primary point of contact for investigator sites, managing site activation, recruitment support, and data quality throughout the study lifecycle.
You will provide strategic medical leadership and expert scientific guidance across project teams to ensure high-quality medical affairs delivery. Additionally, you will ensure compliance with regulatory standards and represent the department in business development initiatives.
The Clinical Trial Central Screener will perform centralized clinical support for patient screening, including clinical trial patient identification and remote chart review. They will also serve as a liaison between network sites and the operations team to facilitate precision medicine software utilization and process improvements.
The Field Senior Clinical Research Associate manages clinical site monitoring activities to ensure adherence to Good Clinical Practice and regulatory guidelines. They serve as the primary point of contact for investigative sites, supporting study start-up, enrollment tracking, and data management tasks.
The Senior Specialist manages the day-to-day Accounts Payable operations, including invoice processing, purchase order creation, and month-end close activities. They also mentor staff, improve departmental metrics, and serve as the primary point of contact for vendor inquiries.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Responsibilities include conducting site visits, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data collection.
The Medical Director acts as a global or regional medical advisor, providing support for clinical protocols, patient safety, and eligibility determinations. They also perform medical reviews of adverse events, serious adverse events, and clinical study reports in collaboration with the pharmacovigilance department.
The Site Navigator coordinates site-level activities throughout the clinical study lifecycle, serving as the primary point of contact for investigative sites. Responsibilities include managing site activation, ensuring regulatory compliance, negotiating contracts and budgets, and maintaining essential study documentation.
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The Clinical Team Lead owns the clinical delivery of research trials, functioning as the project manager to ensure successful execution within budgetary and contractual requirements. They drive project strategy, manage clinical risks, oversee vendor performance, and lead high-performing teams in a matrixed environment.
The Sr. Manager leads cross-functional teams in the operational planning and execution of global clinical trials from start-up to closeout. They are accountable for trial-level delivery, including budget management, vendor oversight, and ensuring compliance with global health authority regulations.
The Senior CRA will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Responsibilities include conducting site visits, resolving issues, and collaborating with cross-functional teams to ensure accurate data collection.
Lead cross-functional project teams to deliver Phase I-IV clinical trials from start-up through closeout while managing project timelines, quality, and budgets. Serve as the primary client contact and drive collaboration across internal stakeholders, external partners, and vendors.
The Executive Director defines and leads the global strategy for site engagement and partnerships to accelerate clinical development and improve patient access. They are responsible for establishing the strategic framework, operating model, and performance KPIs while advising senior leadership on ecosystem trends and investment priorities.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site or remote visits to assess regulatory adherence and manage documentation throughout the clinical trial lifecycle.
The Coder Physician is responsible for abstracting, coding, and sequencing medical records using ICD-10-CM and CPT codes to ensure accurate reimbursement and compliance. They must maintain a 95% quality rating while documenting productivity in specified systems.
You will support the planning and execution of digital marketing campaigns and assist in creating optimized content across various channels. Additionally, you will monitor campaign performance and conduct market research to identify opportunities for improving patient recruitment.
The Legal Counsel will draft and negotiate international commercial agreements while providing guidance on US commercial law, data privacy, and AI governance. They will also support the legal team in navigating clinical research regulations and developing efficient legal processes using modern technology.
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The Clinical Research Associate is responsible for supporting clinical development projects and ensuring that customer goals are achieved. They work alongside innovative professionals to deliver tailored clinical research services across various therapeutic areas.
You will build and maintain strong relationships with clinical trial site staff while providing guidance on study protocols and regulatory requirements. Additionally, you will monitor site performance metrics and implement engagement strategies to optimize clinical trial outcomes.
The Senior CRA will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Responsibilities include monitoring clinical sites, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data collection.
The Clinical Operations Manager is responsible for the performance, compliance, and financial oversight of assigned clinical trial protocols within a country. They manage site budgets, clinical trial agreements, and regulatory submissions while ensuring adherence to quality standards and local regulations.
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