2,326 Clinical Research jobs available for remote work from home. Apply for positions such as Senior Contract Associate, Clinical Site Contracts, Coder Physician, AI Product Manager (EU), and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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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.
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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.
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.
Prepare and submit regulatory documents to the IRB, FDA, and IBC for oncology clinical trials. Maintain the Investigator Site File and serve as the primary point of contact for sponsors, CROs, and regulatory bodies.
Lead the Clinical Operations team by managing CRAs and overseeing clinical trial logistics and biospecimen acquisition. Ensure high-quality end-to-end management of clinical studies while maintaining compliance with regulatory standards.
The Senior Proposals Writer is responsible for crafting compelling and accurate proposals for clinical trials and research projects. This involves collaborating with cross-functional teams and ensuring all documents meet client requirements and regulatory standards.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Ensure compliance with regulatory requirements, informed consent, and safety reporting through remote and on-site monitoring.
The Centralized Monitoring Lead will oversee the Centralized Monitoring team and partner with project and clinical leads to ensure project objectives are met. Responsibilities include managing clinical deliverables, project resources, and developing monitoring strategies.
Responsible for the service delivery of inpatient Clinical Documentation Improvement (CDI) offerings, including managing global teams and defining operational workflows. The role involves overseeing quality assurance, managing client relationships, and ensuring financial profitability of CDI services.
Lead and govern a portfolio of EU Commission and regulatory-funded projects, ensuring full compliance with grant agreements and financial regulations. Manage relationships with international consortium partners and coordinate cross-functional execution to meet scientific and commercial commitments.
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Coordinate day-to-day remote clinical trial operations and facilitate remote patient visits including scheduling and documentation. Manage data entry in EDC and CTMS systems while serving as a virtual liaison between sponsors, CROs, and internal teams.
Oversee and manage early phase clinical programs in collaboration with Contract Research Organizations (CROs). Responsible for strategic planning, financial tracking, and ensuring compliance with FDA and ICH GCP guidelines.
The IRB Vice Chair chairs convened IRB meetings and conducts expedited reviews to ensure compliance with federal, state, and local regulations. They lead the Other Events Committee and collaborate with Principal Investigators and leadership to protect human subject research.
Lead the product roadmap and strategy for a clinical data platform used by a major pharmaceutical company. Coordinate between technical teams and clinical stakeholders to translate complex workflows into executable product requirements.
Oversee day-to-day accounting operations, including general ledger activities, multi-entity consolidations, and the month-end close process. Provide technical accounting support and maintain internal controls to ensure accurate financial reporting and compliance.
Coordinate and execute clinical trial monitoring activities, including study setup and the maintenance of accurate documentation. Build collaborative relationships with investigators and site staff to ensure patient safety and regulatory compliance.
The Study Oversight Manager leads the resourcing and performance of FSP suppliers at the country level to ensure high-quality clinical trial results. This includes acting as the main liaison for supplier capacity, monitoring performance metrics, and supporting inspection readiness.
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The role involves performing site selection, initiation, monitoring, and close-out visits for a specific pharma client. Responsibilities include managing regulatory submissions, tracking recruitment, and ensuring the quality and integrity of site practices.
Identify and engage potential participants for clinical trials through phone interviews and medical history screenings. Coordinate recruitment efforts, schedule appointments, and perform administrative tasks to support study efficiency.
Lead the marketing organization to drive growth strategy, overseeing brand, product marketing, and commercial operations with a focus on health plan partners. Translate complex clinical data into compelling narratives to accelerate payer adoption and strengthen the company's market position.
Oversee the management, maintenance, and compliance of the Trial Master File (TMF) across multiple clinical research studies. Lead a team to ensure documentation is accurate, complete, and ready for regulatory audits and inspections.
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