2,253 Clinical Research jobs available for remote work from home. Apply for positions such as Regulatory and Site Start Up Specialist, Regulatory and Site Start Up Specialist, Clinical Expert, Onco-Immunology, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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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.
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.
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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.
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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The Oncology Data Specialist is responsible for abstracting cancer cases from electronic medical records into registry software and ensuring compliance with state and national reporting standards. Duties include performing case finding, follow-up, and resolving edits prior to submission to the State Central Registry and NCDB.
The eSource Developer III designs and builds electronic source documents aligned with protocol requirements while ensuring quality and usability. This role involves programming logic, mentoring new team members, and collaborating with cross-functional stakeholders to maintain standards-based workflows.
The Clinical Trial Manager oversees the planning, implementation, and management of clinical trials to ensure regulatory compliance and efficiency. This includes coordinating cross-functional teams, managing external vendors, and maintaining study budgets and timelines.
Responsible for drafting, negotiating, and finalizing complex clinical site contracts and budgets throughout the study lifecycle. Acts as the primary liaison between clinical operations, legal teams, and investigator sites to ensure timely execution and compliance.
The Coder Physician reviews medical records to assign accurate diagnosis, procedure, and charge codes for reimbursement and research purposes. They are responsible for abstracting clinical information from various medical records while maintaining strict patient confidentiality and HIPAA compliance.
Develop and scale AI-powered clinical applications using LLMs to streamline pharmaceutical workflows. Lead the product lifecycle from conception to delivery, coordinating with engineering and QA teams to implement scalable AI solutions.
Design and implement advanced data models and machine learning algorithms to solve complex business problems and drive strategic insights. Collaborate with cross-functional teams to translate business needs into analytical solutions and provide thought leadership on data science best practices.
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
The Scientific Director provides strategic ownership of accounts, leading medical communication strategies and overseeing content excellence. They are responsible for managing a team of writers and maintaining senior-level client relationships.
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Responsible for driving revenue growth through new logo acquisition and expanding existing client services within the healthcare industry. This involves outbound prospecting, managing executive-level relationships, and selling the full suite of RCM and clinical management products.
Lead the development and delivery of global Medical Affairs plans and strategies for Neuromuscular programs. This includes managing KOL engagement, publication planning, and collaborating with cross-functional teams to drive clinical outcomes.
Lead the development and delivery of Global Medical Affairs plans and strategies for Neuromuscular programs. This includes managing KOL engagement, publication planning, and collaborating with cross-functional teams to drive clinical outcomes.
Lead the strategy and execution of transitioning the Trial Master File function from an outsourced to an in-house model. Ensure all study TMFs are inspection-ready and aligned with global regulatory expectations through governance and quality control.
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