2,329 Clinical Research jobs available for remote work from home. Apply for positions such as Senior Manager, Clinical Site Partner (Italy), Vision Scientist, Senior Client Delivery Representative, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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Lead the operational execution of Phase I–III oncology clinical trials across Europe, serving as the primary point of contact for clinical sites. Drive site selection, activation, and recruitment while ensuring high standards of performance and quality throughout the study lifecycle.
Conduct scientific and regulatory reviews to evaluate the safety and effectiveness of new ophthalmic devices for the FDA. Prepare comprehensive memos and recommendations regarding submission clearance, approval, or disapproval for various medical device actions.
Lead complex enterprise client implementations from kickoff through deployment, serving as a trusted advisor to senior stakeholders. Coordinate with cross-functional teams to translate business requirements into technical specifications and ensure successful project execution.
The Coder Physician reviews medical records to assign accurate diagnosis, procedure, and charge codes for reimbursement and quality evaluation. They are responsible for abstracting clinical information from various medical records while maintaining strict patient confidentiality and HIPAA compliance.
Lead end-to-end data management for complex global clinical trials from setup to database lock. Serve as the primary client contact while overseeing data reconciliation, budgets, and the mentoring of junior staff.
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Provide expert consultation on RTSM and DHT study design, translating complex requirements into functional project specifications. Manage the delivery of project deliverables while collaborating with stakeholders and external clients to mitigate risks.
Independently lead global clinical projects within the Auto Immune area, managing budgets, scope, and cross-functional teams. Serve as the primary point of contact for clients and oversee all functional areas including data management, safety, and biostatistics.
Independently lead global clinical projects within the Auto Immune area, managing budgets, scope, and cross-functional teams. Serve as the primary point of contact for clients and oversee all functional areas including data management, safety, and biostatistics.
Independently lead global clinical projects within the Auto Immune area, managing budgets, scope, and cross-functional teams. Serve as the primary point of contact for clients and oversee all functional areas including data management, safety, and biostatistics.
Manage country-level regulatory and site activation activities, including EU CTR submissions and the maintenance of Essential Document Packages. Act as the primary contact for investigative sites and coordinate approvals from regulatory authorities and ethics committees.
Lead the development and management of investigator grants and site budgets for clinical trials across the LATAM region. Oversee the grant administration team to ensure accurate payment processing, financial reporting, and compliance with Clinical Trial Agreements.
Lead the development and management of investigator grants and site budgets for clinical trials across the LATAM region. Oversee the grant administration team, ensuring accurate payment processing, financial reporting, and compliance with Clinical Trial Agreements.
Responsible for planning and executing import and export activities for clinical studies, including preparing license submissions and coordinating transactions to depots. The role involves maintaining metrics and problem-solving challenges to ensure compliance with PPD and client requirements.
Responsible for the timely delivery of site activation readiness and the preparation of submission dossiers for Competent Authorities and Ethics Committees. The role involves coordinating with CRAs and project teams to manage essential documents and ensure compliance with local and international regulations.
Responsible for the timely delivery of site activation readiness and the preparation of submission dossiers for Competent Authorities and Ethics Committees. Coordinates with CRAs and project teams to manage essential documents and ensure compliance with local and international regulations.
The Clinical Expert will drive the clinical and scientific strategy for digital twin and data generation programs, focusing on onco-immunology. They will collaborate with science and data teams to prioritize clinical questions, interpret model outputs, and manage academic and pharmaceutical partnerships.
Own and scale the operational lifecycle of biomedical data partnerships, serving as the technical bridge between external partners and internal engineering teams. Manage secure data transfers, harmonization of multi-omics datasets, and the automation of ingestion pipelines.
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Supports early clinical development in inflammation by contributing to protocol development, study start-up, and data analysis. Coordinates cross-functionally to ensure high-quality clinical data for internal decision-making and regulatory submissions.
Provide clinical and sales support by educating customers and providing technical assistance to physicians during Structural Heart procedures. Collaborate with Territory Managers to ensure positive patient outcomes and implement product marketing strategies.
The role focuses on executing compliant study start-up activities and managing regulatory submissions to IRBs/ECs. It also involves leading the migration of regulatory data from Complion to Florence eRegulatory.
Perform detailed review and analysis of cardiac CT scans to support patient eligibility and procedural planning for global TAVR clinical studies. Collaborate with multidisciplinary teams and physicians to ensure consistent imaging assessments and protocol compliance across international sites.
Responsible for driving clinical trial strategies and study designs for diagnostic products in the US and EU regions. This includes acting as a liaison with regulatory bodies and partnering cross-functionally to align clinical programs with market access needs.
Lead commercial growth by identifying high-value opportunities and securing complex development and manufacturing programs for CDMO services. Manage the full business development cycle from prospecting to closing while fostering long-term relationships with biotech and pharma clients.
The MSL serves as a scientific resource to healthcare providers, engaging in the exchange of clinical data regarding Alzheimer's disease and Eisai's pipeline. They are responsible for cultivating relationships with Key Opinion Leaders and gathering medical insights to refine strategic medical plans.
The role involves managing the full spectrum of clinical investigator engagement and designing site-level strategies to ensure predictable enrollment and data delivery. It also requires acting as a scientific ambassador to align investigators with protocol intent and therapeutic objectives.
Accountable for the strategic development and delivery of decentralized and hybrid clinical trials while optimizing speed, quality, and cost. This role involves managing customer relationships, overseeing project financials, and collaborating across functional teams to ensure regulatory compliance.
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Promote and support Abbott Structural Heart surgical valves by developing business growth strategies and managing customer contracts. Collaborate with healthcare providers and clinical staff to generate referrals and ensure positive patient outcomes.
Monitor the progress of clinical studies at investigative sites or remotely to ensure trials are conducted according to protocol. Ensure all recording and reporting align with SOPs, ICH-GCP, and applicable regulatory requirements.
Promote and support Abbott Structural Heart surgical valves by developing business growth strategies and managing assigned accounts. Collaborate with healthcare providers and surgeons to generate referrals and ensure positive clinical outcomes for patients.
Responsible for developing and negotiating Clinical Trial Agreements (CTAs) and site budgets to ensure timely study start-up. This includes liaising with legal departments, managing contract tracking databases, and ensuring compliance with global SOPs.
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