Boston, Massachusetts, United States · Remote OK
$81k–$136k/yr
Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project life cycle in accordance wi…
Skills: Biostatistical Methods, Clinical Trial Design, Statistical Analysis, Data Management, Statistical Planning
Mumbai, Maharashtra, India · Remote Solely
Provide administrative, clerical, implementation and/or processing support to the project teams and stakeholders. Assist with document/process/report development, testing, tracking, distribution, and management. Coordina…
Skills: Clinical Research, Project Coordination, Document Management, Communication Skills, Cross-functional Collaboration
Belgrade, Central Serbia, Serbia · Remote OK
Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale. In-house based position, resp…
Skills: Clinical Site Monitoring, GCP Best Practices, Site Recruitment, Project Management, Regulatory Filings
Warsaw, Masovian Voivodeship, Poland · Remote OK
Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale. In-house based position, resp…
Skills: Clinical Site Monitoring, GCP Best Practices, Site Recruitment, Project Management, Regulatory Filings
Sydney, New South Wales, Australia · Remote OK
Job Title: Administrative Generalist Job Location: Australia Job Type: Full-time Permanent Department/Unit Name: Clinical Operations & Project Management - Site Start-Up Provide administrative support and assistance to t…
Skills: Attention To Detail, Microsoft Office Suite, Document Management, Administrative Support, Scheduling
London, Ontario, Canada · Hybrid
$42k–$70k/yr
Support Trial Master File (TMF) activities to ensure TMFs are “inspection ready” throughout study lifecycle and TMF documents are filed contemporaneously. Primarily responsible for document attribute review, processing, …
Skills: TMF Management, Document Review, ALCOA Principles, Microsoft Office, Archiving
Paris, Ile-de-France, France · Remote OK
Support Project Management, Regulatory, and Contract and Legal in all site-related start-up activities. Establish relationships with study personnel at sites and act as main Alimentiv contact during site start-up. Prepar…
Skills: Site Start-Up, Contract Negotiation, Budget Negotiation, Regulatory Compliance, Project Management
Antwerp, Antwerp, Belgium · Remote OK
Support Project Management, Regulatory, and Contract and Legal in all site-related start-up activities. Establish relationships with study personnel at sites and act as main Alimentiv contact during site start-up. Prepar…
Skills: Site Start-Up, Regulatory Affairs, Contract Negotiation, Budget Negotiation, Project Management
Boston, Massachusetts, United States · Remote OK
$98k–$163k/yr
This opening is for our Medical Research & Development team. Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and…
Skills: Biostatistical Methods, Clinical Trial Design, Statistical Analysis, SAS Programming, Data Management
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Apply biostatistical methods to support clinical trials, including statistical planning, analysis, and reporting throughout the project life cycle. Act as a subject matter expert providing guidance to project teams and contributing to the publication of research data.
Requires expertise in biometrical trial technologies and the ability to translate scientific questions into statistical hypotheses. Must be capable of preparing statistical analysis plans and ensuring adherence to regulatory standards.
Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project life cycle in accordance with project, organizational and regulatory standards. Act as subject matter expert, providing statistical support to project teams, quality/study auditors, and external stakeholders. Participate in the promotion of Alimentiv as a global research organization, by contributing to the development, publishing, and reporting of project data.
\nAnalysis ServicesIndustry-leading specialty GI contract research organization (CRO) transforming clinical trial outcomes and accelerating the development of life-changing therapies. We bring together deep GI expertise, advanced medical imaging solutions, clinical operation excellence and cutting-edge precision medicine/laboratory services. With a global network of 5,000+ sites in >60 countries and growing, we expedite study activation and maximize patient enrollment, ensuring efficient and impactful clinical trials. Trusted by pharmaceutical and biotech partners, we support over 70% of all IBD compounds in development today – delivering customized end-to-end solutions to bring novel therapies to market. As a full-service CRO, our offering is tailored to meet your specific clinical research needs: • Clinical Trial Services • Medical Monitoring • Medical Imaging Solutions • Medical Research & Development • Medical Writing • Precision Medicine/Biomarkers • Clinical Pharmacology • Histopathology via Specialty Lab, AcelaBio • Spatial Biology • Statistics • Real-World Evidence Headquartered in London, Ontario, Alimentiv operates with globally across Canada, the US, Europe, Asia-Pacific, and Latin America.
Offices: 800 Collip Circle, 104, London, Ontario N6G 4X8, CA · 6220 Greenwich Dr, 101, San Diego, California 92122, US · Pietersbergweg 17, Amsterdam, NL · Suite 6, Level 2 29-31 Lexington Drive, Bella Vista , NSW 2153, AU · 150 King St W, Toronto, Ontario M5H 1J9, CA
Industry-leading specialty GI contract research organization (CRO) transforming clinical trial outcomes and accelerating the development of life-changing therapies. We bring together deep GI expertise, advanced medical imaging solutions, clinical operation excellence and cutting-edge precision medicine/laboratory services. With a global network of 5,000+ sites in >60 countries and growing, we expedite study activation and maximize patient enrollment, ensuring efficient and impactful clinical trials. Trusted by pharmaceutical and biotech partners, we support over 70% of all IBD compounds in development today – delivering customized end-to-end solutions to bring novel therapies to market. As a full-service CRO, our offering is tailored to meet your specific clinical research needs: • Clinical Trial Services • Medical Monitoring • Medical Imaging Solutions • Medical Research & Development • Medical Writing • Precision Medicine/Biomarkers • Clinical Pharmacology • Histopathology via Specialty Lab, AcelaBio • Spatial Biology • Statistics • Real-World Evidence Headquartered in London, Ontario, Alimentiv operates with globally across Canada, the US, Europe, Asia-Pacific, and Latin America.
Offices: 800 Collip Circle, 104, London, Ontario N6G 4X8, CA · 6220 Greenwich Dr, 101, San Diego, California 92122, US · Pietersbergweg 17, Amsterdam, NL · Suite 6, Level 2 29-31 Lexington Drive, Bella Vista , NSW 2153, AU · 150 King St W, Toronto, Ontario M5H 1J9, CA
