2,591 Clinical Research jobs available for remote work from home. Apply for positions such as Senior Medical Science Liaison, Rheumatology - Pacific Northwest, Clinical Research Manager, Experienced CRA - Real World Evidence with SSU experience, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Senior Medical Science Liaison serves as a field-based scientific expert, developing relationships with key thought leaders and healthcare providers to facilitate evidence-based scientific exchange. They are responsible for implementing scientific engagement plans, identifying unmet medical needs, and providing clinical insights to inform internal medical strategy.
The Clinical Research Manager oversees day-to-day clinical operations, ensuring study delivery aligns with protocols, SOPs, and regulatory requirements. They also lead and support Clinical Research Associates while serving as the primary operational contact for sponsors.
Perform site monitoring, management, and start-up activities for Real World Evidence studies while ensuring compliance with protocols and regulations. Coordinate regulatory submissions, site activation, and ongoing communication to drive study timelines and data integrity.
Manage investigative sites across Spain to ensure clinical trials adhere to study protocols, ICH-GCP, and regulatory standards. Responsibilities include conducting site visits, performing source data verification, and maintaining Trial Master File documentation.
The Project Leader will manage medium to high complexity clinical trials, ensuring accountability for deliverables, budgets, and quality standards. They will also lead cross-functional teams and maintain strong client relationships to drive study success and operational excellence.
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The Informed Consent Specialist is responsible for developing, reviewing, and approving Informed Consent Forms (ICF) and Subject Information Sheets to ensure regulatory compliance. They also collaborate with stakeholders to manage approval timelines and resolve queries from Ethics Committees and Institutional Review Boards.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Additionally, you will conduct site visits, resolve performance issues, and collaborate with cross-functional teams to ensure accurate data collection.
The Expanded Access Manager will lead the operational support for post-trial managed access programs, including budget coordination and vendor management. They will collaborate with cross-functional teams to ensure regulatory compliance and continuity of access for patients.
You will manage the day-to-day execution of clinical trials, acting as the primary technical and clinical partner for investigators and hospital staff. This involves providing hands-on support during electrophysiology procedures and ensuring site readiness throughout the study lifecycle.
The Senior Clinical Research Associate is responsible for site qualification, initiation, monitoring, and close-out visits in accordance with GCP and regulatory standards. They also act as a Lead CRA for global studies, coordinating monitoring activities and ensuring data quality and site compliance.
The Virtual Physician Assistant will treat patients via tele-health visits, including telephonic triage, video appointments, and email follow-ups. They will collaborate with virtual and in-office teammates to provide evidence-based primary care in a team-based environment.
The role involves providing virtual clinical care through tele-health visits, including triage calls, video appointments, and email follow-ups. Providers will collaborate with virtual and in-office teams while participating in continuous learning through clinical rounds.
The position provides medical leadership and oversight for pancreatic and colorectal cancer programs, including clinical strategy, protocol development, and regulatory execution. The role involves leading clinical study subteams, monitoring data integrity, and collaborating with cross-functional teams to advance the company's oncology portfolio.
The Medical Science Liaison serves as a field-based scientific resource, engaging in the exchange of clinical data with healthcare providers and key opinion leaders. They are responsible for supporting Eisai's strategic medical objectives, mentoring team members, and facilitating research initiatives.
The Senior Director of Business Intelligence will lead the business analytics function, overseeing strategic development and operational execution of data initiatives. They will collaborate with executive leadership to transform complex business problems into scalable data solutions while ensuring data governance and security.
The specialist will manage end-to-end site activities from feasibility to closure, serving as the primary point of contact for investigative sites. They are responsible for regulatory submissions, essential document tracking, and providing updates to cross-functional study teams.
The Clinical Development Director will lead late-phase clinical studies for the maridebart cafraglutide program, overseeing study design, protocol development, and medical monitoring. They will also collaborate cross-functionally to analyze clinical data, author regulatory submissions, and represent the company to key opinion leaders.
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The Quality Operations Manager supports quality management systems by collaborating with operational teams on study document reviews, CAPA management, and database testing. They also lead audit preparation, facilitate vendor audits, and ensure compliance with FDA regulatory requirements and company SOPs.
The specialist proactively drives and executes start-up and maintenance activities for clinical studies and sites in Chile. They serve as the single point of contact for investigative sites and project teams while ensuring adherence to SOPs and project timelines.
The role serves as the primary resource for clinical research metrics, reporting, analytics, and data visualization across the research enterprise. Responsibilities include developing dashboards, reconciling financial data, and providing system support for clinical trial management systems.
The Senior CRA is responsible for site monitoring activities, including study start-up, site initiation, and source data verification for 2-3 clinical trials. They also act as the main contact for site staff, manage investigational products, and ensure compliance with safety reporting and regulatory requirements.
Conduct regulatory audits of COG institutions by reviewing IRB submissions, informed consent documents, audit findings, and site corrections, and prepare and distribute audit reports. Review protocol deviations, early closure requests, and regulatory documents for compliance, coordinate with sites and relevant organizations, and maintain related procedures, templates, and guidance.
Lead and oversee the company’s global privacy, ethics and compliance, and enterprise risk management programs, including policies, assessments, training, monitoring, investigations, and remediation. Advise senior stakeholders, manage regulatory engagement, and promote a culture of integrity and accountability across the organization.
Manage site start-up and activation activities, including preparing and coordinating regulatory and Ethics Committee submissions and maintaining essential site documentation in compliance with Mexican regulations and ICH-GCP. Work with sites and cross-functional teams to meet activation timelines, assess readiness, resolve operational challenges, and maintain effective stakeholder relationships.
Lead the preparation and submission of regulatory documents and coordinate with internal and external stakeholders to secure approvals and authorizations for study initiation. Maintain accurate regulatory records, advise study teams on start-up requirements, and contribute to process improvements.
The Site Activation Specialist manages site feasibility, regulatory documentation, and contract negotiations for clinical research projects. They serve as the primary point of contact for investigative sites and ensure all project timelines and SOP requirements are met.
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Lead clinical study delivery, coordinating cross-functional teams and ensuring studies meet contractual requirements, timelines, quality standards, and financial objectives. Manage customer and vendor relationships, risks, scope changes, project reporting, and team development while identifying opportunities to improve delivery.
Conduct and oversee clinical trial site monitoring, including site visits, source data verification, regulatory documentation, investigational product accountability, and compliance with protocols, ICH GCP, and applicable regulations. Guide and mentor CRA colleagues, coordinate with sponsors and cross-functional teams, resolve site and data issues, and support study planning, reporting, and quality.
Independently conduct and oversee clinical trial site monitoring, including site visits, source document verification, regulatory documentation, investigational product accountability, and compliance with protocols, ICH GCP, and applicable regulations. Guide and mentor CRA team members, coordinate with sponsors and cross-functional teams, resolve site and data issues, and support study planning, recruitment, reporting, and quality activities.
Conduct and oversee clinical trial site monitoring activities in Belgium and the Netherlands, including site visits, source document verification, regulatory documentation, investigational product accountability, and compliance with protocols and GCP requirements. Provide guidance and mentoring to CRA colleagues, coordinate with sponsors and cross-functional teams, resolve site issues, and support study quality, recruitment, and delivery.
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