2,591 Clinical Research jobs available for remote work from home. Apply for positions such as Senior Clinical Database Developer (RAVE) (Home Based - South Africa), Oncology Data Manager, Senior Clinical Research Associate – Phase 1 & Data Readiness, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Senior Clinical Database Developer will design and develop clinical trial databases, data entry screens, and edit checks while ensuring data integrity. They will also conduct user acceptance testing and provide technical support for EDC systems throughout the study lifecycle.
The Oncology Data Manager oversees daily cancer registry and abstracting operations, ensuring compliance with regulatory standards and client requirements. They are responsible for staff management, performance monitoring, and maintaining the integrity of oncology data systems.
The Senior CRA will independently conduct onsite and remote monitoring activities for a Phase 1 clinical study to ensure data accuracy and inspection readiness. Responsibilities include resolving data-readiness gaps, managing regulatory documentation, and collaborating with cross-functional teams to meet database lock milestones.
The Senior Clinical Trial Manager will lead day-to-day clinical trial operations for early-phase gene-editing therapeutics, managing study execution from start-up through close-out. This role involves overseeing CROs, vendors, and investigative sites while ensuring compliance with GCP and regulatory standards.
The Clinical Trial Liaison will drive site engagement and strengthen investigator relationships to advance oncology clinical research. They will serve as a strategic link between research sites and study teams to improve trial performance and patient recruitment.
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The specialist will identify and evaluate paediatric migraine research sites across Europe to accelerate site activation and patient enrolment. They will also build strong relationships with investigators and clinical sites to address recruitment barriers and ensure successful study execution.
The Site Engagement Liaison builds and maintains strong relationships with clinical trial site staff to ensure study compliance and successful conduct. They also monitor site performance metrics and collaborate with internal teams to implement engagement strategies that optimize site performance.
The Clinical Process Change Manager is responsible for driving and managing the development, revision, and retirement of controlled documents to ensure compliant and efficient clinical trial execution. They lead cross-functional initiatives to improve business processes and align operational teams with quality standards and corporate procedures.
The Senior Manager will design and analyze clinical trials while overseeing regulatory affairs operations to ensure compliance and quality. They will lead interactions with regulatory agencies and collaborate cross-functionally to meet global regulatory objectives.
The Junior ERP System Administrator will support the maintenance, administration, and technical troubleshooting of the Priority ERP platform. They will manage user access, configure system settings, and assist with warehouse hardware integrations while collaborating with cross-functional teams.
The Regulatory Affairs Specialist will manage the tracking, archiving, and publishing of regulatory submissions in compliance with ICH and health authority standards. They will also perform quality control checks on documents and coordinate with clinical CROs and third-party vendors to ensure project timelines are met.
The Clinical Lead will oversee the end-to-end execution of clinical trials, including site selection, feasibility assessments, and study progress monitoring. They will also manage study timelines, budgets, and cross-functional collaboration while ensuring strict adherence to GCP and FDA regulations.
Manage the operational aspects of clinical trials from initiation through completion while overseeing site and CRA performance. Lead investigator interactions, coordinate cross-functional study teams, and ensure compliance with FDA requirements and GCP guidelines.
The Associate Director will provide strategic Quality Assurance oversight across clinical research programs to ensure regulatory compliance and quality excellence. They will partner with operational teams to identify quality risks, manage CAPAs, and facilitate inspection readiness.
The Project Manager will coordinate creative and digital projects from initial briefing to final delivery, ensuring they meet quality standards and timelines. They will manage cross-functional teams, external vendors, and internal stakeholders to maintain project momentum and budget control.
The Senior CRA is responsible for monitoring clinical trial sites to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards. They also collaborate with cross-functional teams to manage site performance, ensure data integrity, and provide training to site staff.
The Senior CRA serves as the primary point of contact for clinical trial sites, managing the full lifecycle from start-up to closeout. They are responsible for monitoring site compliance with protocols and ICH-GCP, ensuring data integrity, and overseeing site-level activities.
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You will lead clinical trial start-up and site activation activities while ensuring adherence to sponsor timelines and regulatory standards. Additionally, you will manage project communications and optimize team performance to achieve successful study outcomes.
The RBQM Lead will implement and execute proactive, risk-focused quality oversight across clinical studies throughout the entire trial lifecycle. This role involves facilitating cross-functional risk assessments, leading risk review meetings, and ensuring that mitigation strategies are effectively integrated into study operations.
The Clinical Research Associate II is responsible for delivering quality monitoring reports and ensuring data integrity and patient safety at investigator sites. They will plan and conduct site visits, maintain Trial Master File documentation, and ensure compliance with clinical monitoring plans and regulatory standards.
The Project Manager ensures the efficient implementation of clinical study protocols while managing study budgets, timelines, and compliance with regulatory standards. They serve as the primary contact for sponsors and provide leadership and training to the clinical research team.
You will conduct clinical trial monitoring activities including site qualification, initiation, and close-out visits to ensure protocol compliance and data integrity. Additionally, you will collaborate with investigators and site staff while preparing and reviewing essential study documentation.
The Assistant Clinical Project Manager supports the end-to-end execution of clinical imaging studies by managing project documentation, monitoring deliverables, and coordinating between sponsors and internal teams. They also assist with financial activities, protocol interpretation, and ensure all project operations adhere to regulatory standards and quality requirements.
The Talent Acquisition Specialist will manage the full recruitment lifecycle, including sourcing, screening, and interviewing candidates across various regions. They will also collaborate with line managers to develop recruitment strategies and maintain the ATS to ensure efficient hiring processes.
The Clinical Database Programmer will lead the design, implementation, and maintenance of EDC and clinical database systems to ensure high-quality data delivery. They will also provide technical leadership, mentor programming teams, and serve as the primary liaison for sponsors regarding database programming and regulatory compliance.
The Senior Medical Writer will lead the preparation and delivery of clinical trial transparency submissions while providing strategic regulatory guidance to clients. They are also responsible for mentoring junior team members and ensuring all documentation meets global regulatory standards.
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The General Ledger Accountant will manage monthly close processes, including journal entries, reconciliations, and financial reporting for LATAM entities. They will also support statutory financial statements, tax filings, and cross-functional collaboration to ensure compliance and process efficiency.
The Therapeutic Strategy Director leads the design of innovative clinical development strategies for sponsors from First-in-Human through Phase IIa studies. They are responsible for driving business growth by leading cross-functional teams in proposal development and maintaining high-level client relationships.
The Director will lead the development and execution of the organization's real-world evidence and implementation science research portfolio. This role involves managing end-to-end research operations, fostering sponsor partnerships, and building the infrastructure necessary to scale observational research initiatives.
The Clinical Research Associate is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. They also perform data review and collaborate with investigators to maintain high-quality clinical data throughout the trial process.
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