2,268 Clinical Research jobs available for remote work from home. Apply for positions such as Country Study Operations Manager / Clinical Trial Manager - Canada - FSP, Clinical Sales Specialist, Electrophysiology - LAAO (Albuquerque, NM), Clinical Sales Specialist, Electrophysiology - LAAO (Kansas City, MO), and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Study Operations Manager oversees clinical trial activities from startup through conduct and closeout, ensuring operational delivery and adherence to project plans. They lead local study teams, manage vendor relationships, and coordinate with regulatory bodies to ensure compliance and timely milestone achievement.
The Clinical Sales Specialist provides clinical and sales support by educating healthcare professionals on structural heart products and assisting during procedures. They collaborate with territory managers to ensure optimal clinical outcomes and provide technical expertise to catheter lab staff.
The Clinical Sales Specialist provides clinical and sales support by educating customers on structural heart products and providing technical assistance during procedures. They collaborate with territory managers to ensure positive clinical outcomes and support the implementation of product marketing strategies.
The Senior CRA is responsible for conducting clinical site visits, ensuring protocol compliance, and maintaining effective relationships with site personnel. They also monitor data quality, patient safety, and provide training to site staff while mentoring less experienced team members.
The Clinical Country Site Lead provides local operational and scientific expertise to support global clinical development strategies and ensures successful trial delivery. They act as a key liaison between investigators, research sites, and global study teams while overseeing CRO activities and maintaining regulatory compliance.
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The Associate Clinical Country and Site Lead supports global clinical development strategy by providing local operational and scientific expertise. They serve as the primary point of contact for clinical sites, ensuring quality execution, patient safety, and effective investigator engagement.
The Payment Auditor identifies and recovers incorrectly paid insurance claims by auditing patient accounts and analyzing complex datasets. They act as a liaison between contracting teams and payors to resolve reimbursement issues and monitor revenue recovery metrics.
The Scientific Director will develop high-quality CME content and educational strategies across oncology and hematology. They are responsible for designing educational initiatives, managing faculty, and ensuring all materials meet scientific and regulatory standards.
The Medical Science Liaison serves as a field-based scientific resource, engaging with healthcare professionals to exchange clinical data and medical insights regarding Alzheimer's disease. They are responsible for fostering relationships with key opinion leaders and supporting the company's medical strategy through research and educational initiatives.
The Site Activation Lead manages day-to-day site start-up and activation activities while providing guidance and mentoring to the FSP Site Start Up team. They partner with Clinical Operations to improve study start-up metrics, ensure adherence to project plans, and drive sites to be 'Ready To Enroll'.
The Clinical Sales Specialist provides clinical and sales support by educating customers on Structural Heart products and offering technical assistance during procedures. They collaborate with Territory Managers to ensure optimal case coverage and clinical outcomes for patients.
The Senior Director of Clinical Development is responsible for the design, execution, and analysis of clinical trials to support regulatory approvals and product strategy. This role involves leading cross-functional teams, serving as a medical monitor, and ensuring compliance with scientific and regulatory standards.
The Clinical Research Associate is responsible for managing clinical study sites, ensuring compliance with ICH/GCP regulations, and overseeing protocol adherence. They act as the primary site contact, performing monitoring visits and managing regulatory documentation throughout all phases of clinical trials.
The Associate Director will lead the company's Risk-Based Quality Management strategy and chair the Clinical Data Quality and Governance Board. They are responsible for overseeing central monitoring operations, managing multi-vendor data streams, and driving a proactive, risk-based approach to clinical data quality.
The Associate Director designs and oversees monitoring strategies, including Risk-Based Quality Management and Decentralized Clinical Trial components to ensure data integrity and regulatory compliance. They lead a cross-functional team of remote Clinical Research Associates and act as a primary liaison with CROs and site investigators.
The Senior Medical Science Liaison builds and maintains partnerships with key opinion leaders to facilitate the exchange of scientific data and medical information. They also provide clinical support, identify research opportunities, and represent the company at scientific meetings within the assigned territory.
The Biostatistician provides statistical expertise for clinical research studies, including study design, protocol development, and data analysis. They also support investigators through educational workshops and by authoring statistical sections for research proposals and manuscripts.
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The Clinical Development Lead will oversee the design, execution, and interpretation of clinical trials for hematology-oncology programs. They are responsible for ensuring study integrity, managing regulatory submissions, and collaborating with cross-functional teams to advance the product development strategy.
The Senior Director leads cross-functional clinical program teams to develop and implement operational strategies for oncology clinical trials. They are responsible for managing timelines, budgets, vendor performance, and ensuring compliance with regulatory standards across global studies.
The Medical Director will serve as the Lead Medical Monitor for post-marketing studies, providing medical oversight and ensuring study integrity through rigorous eligibility reviews. They will also contribute to clinical protocol design, safety data interpretation, and the development of global clinical strategies.
Lead scientific dialogue with the patient advocacy community and provide strategic direction for U.S. patient advocacy initiatives in oncology. Represent the company as a key spokesperson while integrating patient perspectives into clinical trial designs and organizational strategy.
The Associate Project Leader will manage day-to-day project activities, including planning, budgeting, and coordinating cross-functional teams to ensure successful delivery. They are responsible for monitoring project progress, identifying risks, and providing regular status updates to stakeholders and senior management.
The Clinical Project Manager oversees a portfolio of projects, acting as the primary client liaison to ensure deliverables are met on time and within budget. They lead cross-functional teams, manage project financials, and provide performance feedback to team members.
The Senior Clinical Research Associate manages investigative site activities and monitoring throughout the clinical trial lifecycle to ensure data integrity and subject safety. They act as the primary contact for sites, facilitating communication and ensuring compliance with protocols, SOPs, and regulatory requirements.
You will coordinate clinical monitoring and site management processes to ensure trials adhere to protocols, ICH-GCP guidelines, and regulatory requirements. This involves conducting on-site or remote visits, managing documentation, and performing root cause analysis to mitigate risks and ensure data reliability.
The QA Specialist III leads quality assurance efforts across a clinical research site network, including conducting complex audits and managing regulatory inspection readiness. They are responsible for developing quality improvement plans, overseeing CAPA implementation, and serving as a subject matter expert for clinical compliance.
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Provide emergency and inpatient radiological coverage for Ochsner Health facilities, including ER and hospital inpatient examinations. Collaborate with a multi-disciplinary team across various specialties such as surgery, transplant, and stroke care.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Key tasks include monitoring clinical sites, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data reporting.
The Project Manager is responsible for leading and coordinating project activities to ensure delivery on time, within budget, and to high quality standards. Key tasks include managing project plans, leading cross-functional teams, and engaging with stakeholders to ensure alignment with organizational goals.
The Country Approval Specialist manages and coordinates country submissions to ensure prompt site start-up and adherence to study timelines. They also collaborate with internal teams and CROs to review essential site documents and resolve escalated issues.
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