2,591 Clinical Research jobs available for remote work from home. Apply for positions such as Senior Clinical Research Associate, Field Clinical Engineer - East, Referral Specialist, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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Independently 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 team members, coordinate with sponsors and cross-functional teams, resolve site and study issues, and support study planning, reporting, recruitment, and quality.
Support clinical study execution at assigned sites, including site start-up, enrollment, follow-up, training, data collection, and protocol compliance. Serve as the field expert on the WiSE System, troubleshoot clinical or device issues, build site relationships, and share feedback with internal teams while supporting process improvement and team mentorship.
Build and manage a country-specific network of referring physicians, providing training, support, and regular visits to promote effective referrals to study investigators. Document discussions and objectives, follow up on agreed tasks, and collaborate with Clinical Operations, Regulatory, and Legal teams to implement referral processes across projects.
Manage and mentor study start-up staff, allocate resources, and coordinate global teams to meet study timelines and quality requirements. Improve start-up processes, monitor metrics and feasibility, support costing and business development, and ensure staff follow company procedures and applicable regulations.
Support the planning and execution of digital marketing campaigns, create and optimize content for websites, newsletters, landing pages, and social media, and contribute to SEO initiatives. Monitor campaign performance, conduct market and audience research, collaborate with internal teams, and provide operational support for marketing projects.
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Develop coverage analysis reports, clinical trial budgets and calendars, charge segregation, and other documentation for industry, federally sponsored, and investigator-sponsored studies. Review and provide feedback on junior specialists’ work, support client contacts, and contribute to clinical research administrative services.
Monitor Phase I oncology trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice, while assessing site performance and resolving issues. Coordinate with cross-functional teams, support accurate data collection and reporting, and train and guide site staff and other CRAs.
Monitor clinical trial sites and conduct site visits to ensure protocol adherence, regulatory compliance, data integrity, and quality trial execution. Collaborate with study teams and site personnel, resolve issues, and provide training and guidance to support successful trial operations.
Lead IDEA projects and manage day-to-day Independent Data Monitoring Committee and endpoint adjudication activities, including project plans, schedules, budgets, and delivery. Coordinate cross-functional teams and stakeholders, monitor progress and risks, communicate status, and support the integration of emerging technologies and innovative solutions.
Translate written materials from English into Korean while preserving the original meaning, structure, and style, and proofread translations for terminology, grammar, spelling, and punctuation. Collaborate with the translation team to maintain and improve glossaries, translation memories, and style guides, identify instruction or project risks, and deliver accurate work on time.
Build and expand strategic partnerships with NHS and other EMEA healthcare organizations, developing tailored growth strategies and securing long-term engagement from senior stakeholders. Represent and promote the TriNetX platform, manage partner accounts and reporting in Salesforce, and serve as a subject matter expert on healthcare data privacy and regulation.
Manage clinical trial sites across the UK through qualification, initiation, monitoring, and close-out, ensuring patient safety, data integrity, and compliance with protocols and regulations. Maintain study documentation, support investigators and study staff, monitor site performance and investigational products, and collaborate with study teams to deliver trials successfully.
Coordinate regulatory submissions, site start-up, activation, and maintenance for assigned studies in Mexico, serving as the country-level contact for sites and internal teams. Collect and review essential documents, track progress and risks, advise on local regulatory requirements, and communicate status and mitigation plans.
Build and manage a network of clinical imaging sites, overseeing site selection, agreements, activation, participant processes, data handling, recruitment tracking, and dataset quality from start to closeout. Develop reusable processes, tools, and reporting systems to scale site operations and deliver complete, quality-checked imaging datasets across required pathologies, scanner vendors, and field strengths.
Support customers through email, chat, and ticket systems by investigating and resolving software issues, coordinating with internal teams, and escalating complex cases. Build customer trust, provide training and product demonstrations, communicate enhancement suggestions, and stay current on application updates.
Build and manage a country-specific network of referring physicians, providing training, support, and regular visits to promote effective collaboration with study investigators. Document discussions and objectives, support completion of agreed tasks, and coordinate with Clinical Operations, Regulatory, and Legal teams to implement referral processes across projects.
Independently conduct remote and on-site monitoring for multicenter clinical studies, including source verification, regulatory document review, site compliance assessment, issue resolution, and reporting. Manage site operations and study tracking, support investigators and study teams, lead centralized monitoring activities, and train junior CRAs.
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Conduct structured and semi-structured interviews with clinical trial participants with Borderline Personality Disorder, administering, scoring, and documenting validated rating scales. Maintain inter-rater reliability and protocol compliance, escalate safety concerns, and collaborate with investigators, site staff, and sponsor or CRO teams.
Manage and develop clinical research associates and study start-up staff, including hiring, onboarding, training, performance reviews, workload oversight, and accompanied site visits. Support country-level study start-up and trial delivery by coordinating regulatory submissions, site activation and enrollment, quality and inspection readiness, and resolution of site risks.
You will support the execution and management of clinical trials by monitoring deliverables and ensuring quality and efficiency. Responsibilities include conducting site feasibility assessments, coordinating with investigative sites, and assisting in the preparation of study documentation.
Manage investigator portals throughout the clinical trial lifecycle, including start-up, maintenance, and archiving. Partner with study teams to implement site engagement strategies and facilitate effective communication with site personnel.
Perform interim monitoring visits at clinical trial sites to ensure protocol adherence and ICH-GCP compliance. Collaborate with project teams to verify study data and manage site action plans.
The Medical Writer II will prepare and edit clinical study reports, protocols, and regulatory documents in compliance with industry standards. They will also conduct literature reviews and analyze clinical data to support the development of scientific manuscripts and presentations.
You will conduct clinical trial monitoring activities, including site visits and ensuring protocol compliance and data integrity. Additionally, you will collaborate with investigators and site staff to facilitate study conduct and prepare essential study documentation.
The Senior Medical Writer is responsible for developing high-quality medical and clinical content, including interpreting clinical data and ensuring compliance with publication guidelines. They also assist in managing medical writing resources, mentoring junior staff, and collaborating with account teams to meet project timelines.
The Clinical Project Assistant will support project managers with the coordination, documentation, and tracking of clinical research studies. They will also assist in maintaining Trial Master Files, managing project communications, and ensuring compliance with regulatory requirements.
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You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while performing data reviews to maintain high-quality clinical documentation.
Supports the Regional Clinical Study Manager in the execution and delivery of clinical studies according to quality standards, timelines, and budget. Manages regional study documentation, system logistics, and site-level activities to ensure operational efficiency and compliance.
You will conduct clinical trial monitoring activities including site qualification, initiation, and close-out visits while ensuring protocol compliance and data integrity. Additionally, you will collaborate with investigators and site staff to facilitate study conduct and prepare essential study documentation.
The Site Management Associate II coordinates monitoring activities at clinical trial sites to ensure adherence to study protocols and regulatory requirements. They also collaborate with cross-functional teams to track site performance metrics and facilitate effective communication throughout the study lifecycle.
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