Remote Clinical Research Jobs (1,576)
Tags = clinical-research
The Clinical Risk Manager will lead risk-based monitoring strategies, including the identification of critical data and processes for global clinical trials. They will also author Integrated Quality Risk Management Plans and serve as a subject matter expert to ensure inspection readiness and cross-functional risk mitigation.
Research Services Intermediate Professional
University of Colorado
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Part Time
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51 mins ago
University of Colorado
The role involves overseeing the day-to-day operations of clinical trials, including subject recruitment, data collection, and ensuring regulatory compliance. The professional will also assist with qualitative research, train junior team members, and manage multiple research projects independently.
US Director, Payor & Access Strategy Lead - Vaccines, Medical Affairs, Health Systems
MSD
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Full Time
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51 mins ago
MSD
The role involves directing and executing US Medical Affairs and Health Systems payor and access strategies while aligning with global medical and commercial goals. The lead will also collect and communicate scientific insights from field engagements to inform company-wide research and commercial strategies.
The Lead Insurance Authorization Specialist coordinates the financial clearance process for appointments to optimize reimbursement and minimize financial risk. This role also provides mentorship to the team while managing complex authorization tasks, eligibility checks, and pre-service collections.
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Sr. Study Coordinator
United Biosource Corporation
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Contract, Freelance
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52 mins ago
United Biosource Corporation
The Senior Study Coordinator supports the conduct of clinical research by managing study protocols, ensuring participant safety, and maintaining accurate clinical data. They also coordinate patient journeys, including telehealth visits and home health nursing, while providing mentorship to junior staff.
The Program Head is responsible for the strategic direction, growth, and end-to-end oversight of the Gene Therapy and Rare Disease portfolio within the Neuroscience Business Unit. This role ensures operational excellence, financial performance, and the successful delivery of complex global clinical programs while fostering long-term sponsor partnerships.
Manage day-to-day clinical trial operations, ensuring adherence to timelines, budget, and quality standards. Collaborate with cross-functional teams to implement protocols and maintain strong relationships with investigators and stakeholders.
Facilitate investigator payments while ensuring compliance with clinical trial regulations and financial protocols. Collaborate with internal teams to resolve payment discrepancies and assist in the preparation of financial reports.
The Director of Clinical Operations oversees a team of managers and individual contributors to ensure high-quality, timely project delivery within budget. They are responsible for talent development, resource planning, and driving business growth through client engagement and strategic leadership.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Responsibilities include conducting site visits, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data collection.
The Medical Writer II is responsible for developing and writing clinical trial documents, regulatory submissions, and scientific publications while ensuring accurate interpretation of clinical data. They also assist in managing medical writing resources and support business development activities through research and proposal writing.
Regulatory Coordinator
Nemours Children's Health
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Full Time
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2 hours ago
Nemours Children's Health
The Regulatory Coordinator manages the regulatory lifecycle of pediatric oncology clinical trials, ensuring compliance with federal regulations and institutional policies. They oversee the electronic regulatory binder system, coordinate study start-up activities, and facilitate audit-ready documentation across the enterprise.
The Site Payments Specialist is responsible for configuring and maintaining site payment systems and study budgets to ensure accurate financial operations. They will collaborate with study teams and investigative sites to manage payment requirements, resolve discrepancies, and ensure compliance with clinical trial agreements.
The Investigator Payments Lead manages the end-to-end administration of site and investigator payments across clinical studies, ensuring accuracy and compliance. They also coordinate with vendors, resolve payment discrepancies, and support audit activities to maintain operational efficiency.
The Investigator Payments Lead manages end-to-end clinical trial site payment activities, ensuring accuracy and compliance with contractual agreements. They oversee payment system configurations, monitor vendor performance, and resolve payment-related queries to support study delivery.
Sales Key Account Manager Oncology - Außendienst - Region "Mitte"
Johnson & Johnson Innovative Medicine
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Full Time
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3 hours ago
Johnson & Johnson Innovative Medicine
The Key Account Manager drives sales and business results by executing brand plans and maintaining partnerships within the oncology and hematology therapeutic areas. They act as a product specialist, analyzing territory data to develop account plans and coordinating cross-functional activities to ensure customer interaction excellence.
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The Senior CRA manages clinical monitoring and site management activities to ensure trials are conducted according to protocols, ICH-GCP, and regulatory requirements. They perform remote and on-site monitoring, conduct data verification, and maintain effective communication with investigational sites to ensure data quality and patient safety.
The Investigator Payments Lead manages the end-to-end lifecycle of clinical site payments, ensuring timely and accurate disbursements from study startup to close. They also provide oversight of vendor staff and troubleshoot complex payment issues to maintain site satisfaction and contractual compliance.
The Clinical Trial Associate assists project teams with the setup, organization, and maintenance of clinical study documentation and trial materials. They also perform quality control audits, track trial progress, and serve as a primary contact for clinical sites regarding basic requests.
The Laboratory Study Manager will lead the planning, execution, and monitoring of complex clinical trials while ensuring adherence to regulatory requirements. They will collaborate with cross-functional teams to manage study plans, budgets, and timelines while resolving complex issues to maintain data integrity.
You will be responsible for all site management and supervisory activities for oncology studies while working with industry leaders. Additionally, you will mentor junior CRAs and ensure compliance with clinical research guidelines.
Local Contract Research Nurse (Per Diem) - Naples, Italy
Syneos Health
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Part Time
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5 hours ago
Syneos Health
The Research Nurse will coordinate patient care and facilitate communication between patients and healthcare providers to ensure study protocol compliance. They are responsible for monitoring patient progress, collecting accurate data, and providing individualized support throughout the clinical research process.
The Site Management Associate supports clinical trial site management by assisting with monitoring activities and ensuring adherence to study protocols and regulatory requirements. They also collaborate with cross-functional teams to maintain accurate records and facilitate effective site communication.
The Senior Contract Associate is responsible for drafting, negotiating, and finalizing complex clinical site contracts and budgets throughout the study lifecycle. They serve as the primary point of contact between internal departments and external sites to ensure compliance and timely execution of agreements.
The Clinical Research Associate II coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence, manage documentation, and resolve site-level issues.
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Lead, perform, and report a range of GxP audits across all phases of clinical research to ensure compliance with regulatory requirements. Manage audit programs, coordinate internal audits, and provide consultancy on quality and regulatory compliance to internal and external stakeholders.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams and investigators to manage project components and ensure accurate documentation of monitoring activities.
The Central Review Manager performs centralized review and approval of clinical monitoring visit reports to ensure consistency and protocol compliance. They also liaise with clinical monitoring staff and evaluate site performance, subject safety, and study processes based on monitoring data.
The Computational Statistician will develop and implement statistical analysis plans for clinical trials while collaborating with clinical research associates. They are responsible for establishing reporting databases, conducting peer reviews, and ensuring the accuracy of statistical analyses.
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