2,267 Clinical Research jobs available for remote work from home. Apply for positions such as Director, Business Development, Senior Clinical Project Manager - UK, Senior Safety Reporting Coordinator, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Director of Business Development will drive revenue growth by identifying new leads, managing client relationships, and selling CRO and FSP services. They will also lead proposal development, negotiate contracts, and collaborate with internal teams to execute sales strategies.
The Senior Clinical Project Manager will lead end-to-end delivery of clinical pharmacology projects, overseeing complex studies and managing global cross-functional teams. They are responsible for maintaining project scope, timelines, and budgets while ensuring compliance with regulatory standards and building strong client relationships.
The Senior Safety Reporting Coordinator manages the submission, tracking, and archiving of safety reports while providing administrative support to the Pharmacovigilance department. They also lead projects, mentor team members, and ensure compliance with standard operating procedures.
The Clinical Research Associate will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. They will also coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
You will monitor and manage the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. Additionally, you will coordinate study setup activities, including investigator identification and regulatory submission preparation.
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Lead complex, global cardiometabolic clinical trials from start-up to close-out while ensuring adherence to scope, budget, and timelines. Manage multidisciplinary teams and act as the primary point of contact for sponsors to drive project excellence and regulatory compliance.
Lead the team responsible for building rapid-turn AI solutions, including RPA and AI agents, while balancing direct delivery with citizen-developer enablement. Manage a portfolio of automation initiatives, establish governance standards, and foster relationships with business unit leaders to drive strategic value.
The Senior Coding Specialist will oversee outsourced medical coding activities and ensure the quality and consistency of clinical trial data. They will also serve as a subject matter expert for dictionary usage and support upversioning across global studies.
You will lead clinical trial initiation activities, including site document collection, review, and activation. Additionally, you will collaborate with internal teams and CROs to ensure regulatory compliance and meet project timelines.
This position leads industry-sponsored clinical research budget development and negotiations to ensure financial feasibility and compliance. It also manages continuous quality improvement initiatives for the budgeting program and facilitates the transition of executed budgets into invoicing workflows.
Deliver high-quality diabetic care and education to patients across various settings, including remote consultations. Collaborate with multidisciplinary teams to support holistic patient care and participate in health initiatives.
The Project Manager will oversee IRT system activities from award to closeout, ensuring projects remain within timeline and budget. They will facilitate meetings, manage requirement designs, and proactively communicate with key stakeholders to identify risks and create action plans.
Lead validation activities for study software in accordance with regulatory standards and manage the overall test effort across assigned projects. Review and approve Computer System Validation packages while partnering with cross-functional teams to ensure high-quality, compliant software deliverables.
The Project Manager will lead global clinical trials from start-up to close-out, serving as the primary point of contact for sponsors. They are responsible for managing project budgets, timelines, cross-functional teams, and ensuring compliance with regulatory standards.
The Senior MSL will cultivate relationships with thought leaders to facilitate scientific exchange and provide strategic insights to internal stakeholders. They will also support clinical trial activities, investigator-initiated research, and provide medical education across various healthcare specialties.
The Senior MSL will cultivate relationships with thought leaders through scientific exchange and provide strategic insights to internal stakeholders. They will also support clinical trial activities, investigator-initiated research, and provide medical education across the product lifecycle.
The Senior Clinical Analyst and Programmer will lead programming activities for data review, safety listings, and centralized monitoring reports. They are responsible for gathering requirements from DM and RBSM departments and creating SAS code to meet these needs within budget and timelines.
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You will independently manage the negotiation and execution of clinical trial agreements and budgets while collaborating with internal stakeholders. Additionally, you will monitor contract portfolios, address execution barriers, and support continuous improvement in contract processes.
The Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management and remote monitoring activities. They ensure compliance with SOPs and regulatory guidelines while assisting with site preparedness, document collection, and data reconciliation.
Design and conduct epidemiological studies to generate real-world evidence while ensuring adherence to time, budget, and quality standards. Collaborate with sponsors to analyze observational data and communicate findings to support internal and external decision-making processes.
The representative will serve as the primary contact for patients and medical professionals to assist with program eligibility, card activation, and benefit explanations. They are responsible for documenting resolutions and troubleshooting submission rejections via phone, email, or fax.
The Lead Clinical Study Manager oversees the operational strategy, planning, and execution of clinical studies to ensure compliance with quality standards and budget requirements. They manage relationships with strategic partners and CROs while providing subject matter expertise to support clinical development plans.
The Associate Director provides strategic regulatory guidance for nonclinical development programs, ensuring scientific rigor and compliance for IND, CTA, and NDA/BLA submissions. They lead cross-functional teams and serve as a subject matter expert during health authority interactions to facilitate efficient drug development.
The Clinical Sales Specialist provides clinical and sales support by educating customers on structural heart products and assisting physicians during procedures. They collaborate with territory managers to ensure optimal clinical outcomes and provide technical expertise in the catheter lab.
The Data Coordinator will perform accurate and timely data entry to support clinical trial operations and sponsor-facing activities. They are responsible for maintaining data quality, following structured processes, and managing assigned tasks independently.
The Clinical Sales Specialist provides clinical and technical support to interventional cardiologists and catheter lab staff during procedures. They also educate customers on product usage and collaborate with Territory Managers to drive clinical outcomes and marketing strategies.
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The Clinical Sales Specialist provides clinical and technical support to interventional cardiologists and catheter lab staff during structural heart procedures. They are responsible for educating customers on product usage, managing territory clinical outcomes, and collaborating with Territory Managers to implement marketing strategies.
The Quality Audit Specialist executes internal and external audits while monitoring GCP regulatory compliance across clinical trial operations. They also manage document control activities, track quality metrics, and support continuous improvement initiatives within the electronic Quality Management System.
The Contract Negotiation Specialist is responsible for independently drafting, reviewing, and negotiating clinical trial agreements to support study start-up activities. They act as a primary point of contact for sites and internal teams while ensuring all contracts comply with regulatory requirements and project timelines.
The role involves supporting the mission of Memorial Sloan Kettering Cancer Center in ending cancer through research and specialized care. The resource will contribute to collaborative efforts in translational and clinical research to improve cancer diagnosis and treatment.
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