2,313 Clinical Research jobs available for remote work from home. Apply for positions such as Associate Clinical Research Manager (aCRM) - Infectious Disease/Vaccine, Customer Services Representative I (Patient Collections), Bilingual Customer Services Representative I (Patient Collections), and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Associate Clinical Research Manager is responsible for the end-to-end performance and project management of assigned clinical protocols in compliance with ICH/GCP and company standards. They act as the main point of contact between country operations and clinical trial teams, ensuring deliverables and timelines are met from feasibility through study close-out.
The representative will manage incoming and outbound calls to assist patients with self-pay balances and determine appropriate next steps for accounts. They are also responsible for posting patient payments and adjustments according to standard operating procedures.
The representative will handle incoming and outbound calls to assist patients with self-pay balances and account inquiries. They are also responsible for reviewing patient accounts receivable and accurately posting payments and adjustments according to standard procedures.
The Site Engagement Lead is responsible for building and managing long-term relationships with clinical research sites to optimize trial performance and quality. They will act as the primary point of contact for the PEER site network, driving KPI targets and implementing mitigation plans to address operational bottlenecks.
You will coordinate monitoring activities at clinical trial sites to ensure compliance with study protocols and regulatory requirements. Additionally, you will collaborate with cross-functional teams and track site performance metrics to enhance management efficiency.
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The Senior Grants Analyst oversees the full lifecycle of grants, including application review, compliance monitoring, and financial tracking. They also provide insightful analysis to support organizational funding initiatives and mentor junior team members.
The Respiratory Clinical Program Manager serves as a subject matter expert providing clinical education, consultation, and program leadership across various healthcare settings. They collaborate with sales and product teams to drive business growth, conduct clinical assessments, and support respiratory therapy initiatives.
The specialist will build and cultivate relationships with physicians, healthcare professionals, and community leaders to drive clinical trial recruitment. They will travel regionally to conduct outreach, attend community events, and manage a network to support enrollment goals.
The Patient Recruitment Associate will support patient engagement and retention initiatives while coordinating recruitment campaigns and materials. They will also monitor recruitment performance metrics and collaborate with global teams, sponsors, and vendors to ensure project delivery.
The Senior Manager is responsible for leading clinical operations teams to ensure high-quality, timely project delivery while building and maintaining strong client relationships. They will also oversee staff performance, resource planning, and contribute to strategic business development and internal process improvements.
The Director of Clinical Affairs will define and execute the integrated clinical evidence strategy across the product lifecycle while overseeing clinical study operations. This role involves building clinical infrastructure, managing cross-functional partnerships, and engaging with external scientific stakeholders to support regulatory and commercial objectives.
The Clinical Engagement Regional Associate Director leads a field-based team of Clinical Engagement Leads to manage investigator and site relationships across Europe and Asia. This role serves as a central escalation point and provides strategic oversight for site feasibility, activation, and enrollment performance.
The Clinical Research Associate is responsible for conducting site monitoring visits, including qualification, initiation, routine, and close-out visits for oncology trials. They also manage site documentation, ensure protocol compliance, verify patient eligibility, and maintain clinical data integrity.
Manage day-to-day clinical trial operations, including planning, budgeting, and ensuring adherence to quality standards. Collaborate with cross-functional teams and stakeholders to implement protocols while maintaining regulatory and ethical compliance.
The Clinical Associate provides operational support to study teams by coordinating and overseeing payment-related activities throughout the clinical trial lifecycle. Responsibilities include tracking site payments, reviewing invoices, ensuring contractual compliance, and maintaining accurate financial records.
Provide leadership and direction to the clinical site management team from study start through to closure. Serve as the primary point of contact for clinical monitoring and site activities while managing deliverables to meet study budgets.
Lead the development and support of clinical technology solutions while designing and validating complex SAS programs and datasets. Collaborate with global teams to drive data quality, automation, and the creation of impactful visual analytics dashboards.
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The Clinical Research Associate manages assigned clinical trial sites to ensure compliance with ICH-GCP, study protocols, and regulatory requirements. They act as the primary site contact, overseeing site performance, patient recruitment, and data integrity throughout the study lifecycle.
The Associate Medical Monitor performs medical review and interpretation of adverse events and device deficiencies to ensure clinical trial safety. They also provide medical expertise for clinical study protocols, regulatory submissions, and committee activities like CEC and DSMB.
The Research Finance Specialist manages clinical trial financials, including invoicing, revenue reporting, and financial reconciliations within the CTMS. They also collaborate with research sites to ensure billing accuracy and resolve discrepancies with sponsors and CROs.
The Coder Outpatient is responsible for abstracting, coding, and sequencing clinical information from various medical records to ensure accurate billing and reimbursement. They must maintain compliance with regulatory standards while documenting productivity and meeting quality rating requirements.
The Medical Science Liaison serves as a scientific expert, building relationships with healthcare professionals and key opinion leaders to facilitate evidence-based scientific exchange. They also gather medical insights and support clinical research initiatives to inform the company's medical strategy.
The role involves leading research and scientific community governance processes, including the design of data governance frameworks for biomedical research. You will also drive privacy and compliance initiatives, ensuring adherence to ethical and regulatory standards while fostering responsible data sharing.
The Manager, Clinical Operations will oversee the planning and execution of clinical trials to ensure they meet regulatory standards and timelines. They are also responsible for mentoring junior staff and fostering collaboration across cross-functional teams to optimize operational efficiency.
The Recruitment Strategy Manager will lead the development and execution of strategic participant recruitment campaigns to meet clinical study enrollment goals. They will serve as a subject matter expert, integrating data, marketing insights, and cross-functional collaboration to optimize recruitment performance and budget efficiency.
The Sr. Feasibility Site Specialist manages site feasibility planning, including site list vetting, pre-award outreaches, and document collection. They also serve as a subject matter expert, mentoring team members and driving continuous process improvement initiatives.
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The Medical Manager provides scientific and medical expertise to support Pfizer's genitourinary oncology portfolio while ensuring compliance with local and corporate regulations. They are responsible for managing clinical research collaborations, developing medical affairs plans, and maintaining professional relationships with key opinion leaders and healthcare authorities.
The Project Manager II oversees interdisciplinary clinical research studies, ensuring compliance with regulatory requirements and GCP standards. They are responsible for managing project timelines, budgets, and deliverables while acting as the primary liaison between the company and the customer.
The Clinical Project Manager leads clinical study operations from inception to completion, including strategic planning, budget oversight, and team management. They serve as the primary contact for sponsors and ensure all study activities comply with GCP, regulatory requirements, and project-specific plans.
The Associate General Counsel provides strategic legal counsel on clinical, commercial, and healthcare regulatory matters, including data privacy and EU employment law. They advise cross-functional teams to manage legal risk while supporting responsible innovation and compliant clinical research operations.
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