Manage clinical trial operations, including budget oversight, study start-up, and enrollment activities. Coordinate with sponsors and vendors while mentoring Clinical Research Associates to ensure high-quality study outcomes.
Remote Clinical Research Jobs (1,605)
Tags = clinical-research
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance and data integrity while collaborating with investigators to maintain high-quality clinical data.
The role involves reviewing RFPs to develop strategic proposals, budgets, and scopes of work for customers. It also requires coordinating with internal stakeholders to ensure document quality and maintaining corporate tracking databases.
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.
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.
Senior Clinical Research Associate - Oncology, Hematology - France
Worldwide Clinical Trials
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Full Time
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3 Weeks 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 Weeks 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 Weeks 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 Weeks 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.
Medical Project Coordinator
Thermo Fisher Scientific
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Full Time
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3 Weeks 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.
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.
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Clinical Trials (Business Development Experienced)
Angel City VA
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Full Time
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3 Weeks 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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3 Weeks 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 Operations Lead (Clinical Trial Manager) (India)
Alimentiv
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Full Time
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3 Weeks 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.
Medical Science Liaison, Netherlands
Revolution Medicines
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Full Time
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3 Weeks 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.
Virtual Medical Assistant (Contract – Remote, Philippines)
Health Haven
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Full Time
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3 Weeks 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.
Lead a complex grants and contracts portfolio by coordinating pre-award proposal submissions and post-award financial reconciliation. Manage compliance, budget projections, and partnerships across multiple disciplines and faculty within the School of Medicine.
Director, Medical Science Liaison, Oncology (Dallas, AR, LA, OK, MS)
Revolution Medicines
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Full Time
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3 Weeks Ago
Revolution Medicines
The Director, 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 to support medical strategies and congresses.
Vice President, Site Activation Project Management and Global Regulatory Oversight
ICON plc
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Full Time
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3 Weeks Ago
ICON plc
Provide strategic and operational leadership for the global study start-up organization to ensure timely and compliant initiation of clinical trials. Lead global teams in site activation and regulatory oversight while serving as the executive sponsor for delivery excellence across pharma and biotech portfolios.
The Data Management Lead provides technical expertise and serves as the primary point of contact for assigned studies to ensure quality and timely delivery of data. Responsibilities include managing study timelines, collaborating with cross-functional global teams, and ensuring compliance with regulatory guidelines.
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Responsible for identifying and screening potential clinical trial participants via outbound and inbound calls. Tasks include assessing eligibility based on protocol criteria and scheduling qualified candidates for on-site visits.
Drive revenue growth by securing new clients and expanding services for global clinical operations. Manage the full sales lifecycle from prospecting and relationship building to closing complex, high-value deals.
Manage start-up contracting activities, including developing investigator grant estimates and maintaining contract templates for biotech sponsors. Ensure compliance with regulatory requirements and project timelines while collaborating with stakeholders and RSU regions.
The Principal Statistical Programmer leads clinical sub-teams by delegating tasks, providing technical support, and ensuring the accuracy of SAS code and output. They are responsible for creating necessary files and analyses for electronic submissions in eCTD format while ensuring compliance with FDA/ICH/GCP regulations.
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