The role involves designing and analyzing clinical trials by interpreting complex medical data and maintaining eCRFs and validation specifications. You will manage data reconciliation and communicate study metrics to project teams and management.
Remote Clinical Research Jobs (607)
Tags = clinical-research
Provide advanced technical expertise to develop process methodology and integrated programming solutions for complex clinical studies. Lead technical teams in creating statistical tables, figures, listings, and analysis datasets while coordinating with internal and external clients.
Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)
IQVIA
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Full Time
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3 Days Ago
IQVIA
Manage vendor activities across the global clinical trial lifecycle from start-up to close-out to ensure high-quality deliverables. Monitor vendor performance using KPI/KQI dashboards and manage risks and costs to ensure operational success.
Support the management of clinical trial sites by assisting with monitoring activities and ensuring adherence to study protocols and GCP guidelines. Collaborate with cross-functional teams to maintain accurate records and address site-related issues effectively.
Lead global and regional clinical programs from start-up to close-out while managing and coaching a team of Study Managers. Drive cross-functional collaboration and maintain relationships with external partners, KOLs, and CROs to ensure high-quality study delivery.
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The Principal Biostatistician leads the design, analysis, and interpretation of complex clinical studies, specifically within rare disease and oncology. They are responsible for creating statistical analysis plans, overseeing statistical programming, and ensuring high-quality output for regulatory submissions.
Lead the design, analysis, and interpretation of complex clinical studies, specifically within rare disease and oncology. Responsible for creating statistical analysis plans, overseeing statistical programming, and ensuring high-quality output for regulatory submissions.
Lead the design, analysis, and interpretation of complex clinical studies, specifically within rare disease and oncology. Responsible for creating statistical analysis plans, overseeing statistical output, and collaborating with cross-functional teams to support product development submissions.
Lead the design, analysis, and interpretation of complex clinical studies, specifically within rare disease and oncology. Oversee the creation of statistical analysis plans, protocols, and summary reports while mentoring junior statisticians.
Lead the design, analysis, and interpretation of complex clinical studies, specifically within rare disease and oncology. Responsible for creating statistical analysis plans, overseeing statistical output, and collaborating with cross-functional teams to support product development submissions.
The Principal Biostatistician leads the design, analysis, and interpretation of complex clinical studies, specifically within rare disease and oncology. They are responsible for creating statistical analysis plans, overseeing statistical programming, and ensuring high-quality output for regulatory submissions.
Perform country-level site activation activities and serve as the single point of contact for investigative sites and project management teams. Manage regulatory documents, track approvals, and ensure adherence to SOPs and project timelines.
Senior Clinical Research Associate - Oncology, Hematology - France
Worldwide Clinical Trials
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Full Time
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3 Days Ago
Worldwide Clinical Trials
The role is responsible for managing the full lifecycle of clinical sites, including qualification, monitoring, and close-out visits. It also involves mentoring junior CRAs and ensuring data veracity and protocol compliance.
12 month FTC- Spanish speaking Medical Information Specialist
ProPharma
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Full Time
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3 Days Ago
ProPharma
Provide high-quality medical information services via phone and email, answering technical product questions and handling adverse event reports. Translate medical documents between English and Spanish and ensure all inquiries are logged accurately in compliance with SOPs.
Medical Writer- Publications
Cactus Communications Services Pte. Ltd.
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Full Time
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3 Days Ago
Cactus Communications Services Pte. Ltd.
Develop high-quality scientific and medical materials including manuscripts, posters, and slide decks for pharmaceutical clients. Collaborate with international stakeholders and utilize AI tools to create effective medical communications initiatives in the digital space.
Senior Medical Writer- Publications
Cactus Communications Services Pte. Ltd.
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Full Time
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3 Days Ago
Cactus Communications Services Pte. Ltd.
Develop high-quality scientific materials including manuscripts, posters, and abstracts while ensuring strategic alignment and scientific accuracy. Lead and mentor a team of scientific writers and maintain professional relationships with pharmaceutical clients and key opinion leaders.
Provides leadership for clinical studies and regulatory affairs to ensure product approvals are obtained in a timely and ethical manner. Manages a team of direct reports, focusing on performance management, talent development, and the execution of local and global research projects.
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Lead the design, development, and implementation of advanced clinical systems aligned with study protocols and operational needs. Collaborate with cross-functional teams to drive system enhancements and provide strategic guidance on new clinical technologies.
Medical Project Coordinator
Thermo Fisher Scientific
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Full Time
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4 Days Ago
Thermo Fisher Scientific
Coordinate and review safety data to ensure compliance with regulatory standards and optimal patient safety in clinical trials. Manage project implementation, forecasting, and serve as a primary point of contact for clinical and data management teams.
Responsible for the management, monitoring, and close-out of clinical trial investigator sites to ensure patient safety and quality execution. Acts as the primary point of contact for sites, managing relationships and ensuring compliance with GCP and Pfizer standards.
The Senior Medical Director provides strategic and scientific leadership across multiple brands to ensure the accuracy and impact of medical communications. This role involves overseeing medical strategy, mentoring junior staff, and collaborating with multidisciplinary teams to drive business growth.
Clinical Trials (Business Development Experienced)
Angel City VA
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Full Time
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4 Days Ago
Angel City VA
Identify and engage potential clients such as medical practices and hospitals to expand the clinical trials network. Develop strategic sales plans and maintain strong relationships with key decision-makers to drive growth.
Clinical Trials (Business Development Experienced)
Angel City VA
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Full Time
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4 Days Ago
Angel City VA
Identify and engage potential clients such as medical practices and hospitals to expand the clinical trials network. Develop strategic sales plans and maintain strong relationships with key decision-makers to drive growth.
Lead the design and implementation of data science strategies to enhance clinical trial data analysis and optimize data interpretation. Manage day-to-day activities, mentor team members, and communicate actionable insights to stakeholders to influence project direction.
Clinical Operations Lead (Clinical Trial Manager) (India)
Alimentiv
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Full Time
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4 Days Ago
Alimentiv
The Clinical Operations Lead provides oversight of project deliverables, CRAs, and investigator sites to ensure compliance with protocols and GCP guidelines. They act as the primary liaison between the monitoring team and the clinical project team while managing site performance and recruitment strategies.
Develop and maintain enterprise web applications while supporting modernization and AI-driven initiatives. Collaborate with technical and business teams to troubleshoot issues and deliver new features using clean, scalable code.
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Medical Science Liaison, Netherlands
Revolution Medicines
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Full Time
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4 Days Ago
Revolution Medicines
The MSL will engage in peer-to-peer scientific dialogue with healthcare professionals and KOLs to gather insights and advance medical knowledge. They will serve as a therapeutic expert and liaison between the company and clinical study sites, supporting medical congresses and advisory boards.
Perform and coordinate clinical monitoring and site management to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory requirements. Conduct remote and on-site visits to assess data reliability, manage documentation, and mentor junior clinical team members.
The role involves managing the healthcare revenue cycle by verifying insurance eligibility, submitting claims, and handling denial management. Additionally, the biller will communicate with patients regarding billing inquiries and maintain accurate financial records.
Virtual Medical Assistant (Contract – Remote, Philippines)
Health Haven
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Full Time
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4 Days Ago
Health Haven
The role involves assisting providers with medical charting, EMR management, and chart auditing to ensure documentation quality. Additionally, the assistant manages patient coordination, prior authorizations, and monitors virtual appointments to maintain provider productivity.
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