Clinical Data
405 open positions
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Trial Master File Specialist MedpaceCincinnati, Ohio today Manage the Trial Master File (TMF) to ensure data integrity and support FDA approval for new drugs or devices.
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Senior Clinical Data Manager I AstraZenecaIndia - Bangalore 1d Coordinates Clinical Data Management (CDM) deliverables for assigned clinical studies, ensuring data integrity from build through lock to support regulatory submissions.
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Manager, RIM Governance and Engagement BristolmyerssquibbHyderabad - TS - IN 1d Manage Regulatory Information Management (RIM) system governance, data quality, and global regulatory event workflows to ensure compliance and documentation of regulatory approvals.
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Laboratory Data Analyst IqviaPasig, Philippines 1d Develop and maintain Laboratory Data Management (LDM) tasks for clinical studies, ensuring data reporting needs for external clients are met.
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Senior Central Monitor AbbVieMexico City, CDMX, mx 1d Analyze and investigate clinical trial data at a macro-level using Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs) to identify risks to participant safety and data integrity, acting as the first responder for study-level risks.
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Lead Clinical Research Data Manager UchicagoChicago, IL, US $65k–$65k2d Leads and oversees data management tasks for high-complexity clinical research studies, ensuring protocol adherence and data quality for hematology and oncology research.
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Lead Clinical Research Data Manager↗ The University of ChicagoChicago, IL, US $65k–$65k2d Lead and oversee data management for high-complexity clinical research studies, ensuring protocol adherence and data quality for hematology and oncology research.
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Medical Monitor UscSan Diego, CA, US $99k–$99k2d Provide medical oversight for Alzheimer's disease clinical trials, ensuring conduct, recording, and reporting align with protocols, SOPs, GCP, and regulatory requirements.
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?Lead Clinical Data Manager↗ San Diego, CA, US $152k–$152k2d Lead clinical data management activities across the full study lifecycle, ensuring data quality and compliance for clinical trials.
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Clinical Data Manager↗ Kps LifeMalvern, PA, US 2d Oversee and manage Sponsor's clinical programs regarding data management activities for clinical trials, including vendor management and data feed oversight.
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Associate Director, Clinical Data Management – Oncology↗ Simulstat IncRedwood City, CA, US 2d Lead clinical data management activities and strategy for early- and late-stage oncology studies.
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Senior Medical Coding Specialist IconRemote 2d Ensure accurate and consistent coding of medical data for clinical trials, including independent review of third-party coded data and oversight of outsourced CRO work.
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Senior Manager, Statistical Programming EdwardsUSA-California-Remote $151k–$151k2d Lead statistical programming activities and manage a team to generate clinical evidence for transcatheter heart valve therapies.
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Clinical Research Manager↗ MedartisUS 2d Manage the end-to-end development and execution of clinical research projects, including study protocols, site selection, regulatory compliance, and data collection for orthopedic medical devices.
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Clinical Data Manager↗ The Emmes Company, LLCRockville, MD, US 2d Oversee the collection, processing, and management of clinical trial data to ensure accuracy, completeness, and verifiability per protocol and regulatory guidelines.
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Lead Data Manager for Clinical Trials Psi-CroMississauga, ON, ca 2d Lead all data management activities for large, complex clinical studies, serving as the primary communication point for project teams, clients, and vendors regarding data integrity and reporting.
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Clinical Study Operations Associate BeaconbiosignalsRemote $65k–$65k2d Support the deployment of at-home EEG and cardiopulmonary devices in clinical studies for neurological, psychiatric, and sleep disorder therapeutics.
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Consultant - RTSM VeevaChina - Shanghai 2d Technical Consultant writing custom code and configuring RTSM (Randomization and Trial Supply Management) solutions to help life sciences companies expedite clinical trials.
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Data Manager (Expert in Programming & developing EDC systems) ErgomedPune, MH, in 2d Manage clinical trial data, validate EDC systems, and oversee database lock activities for pharmaceutical studies.
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Data Manager (Rare Anaemia Disorders Research Laboratory)↗ Vall D'hebron Institut de RecercaBarcelona, CT, ES 3d Lead data management and quality assurance for clinical trial-grade research and patient registries on rare haematological diseases, bridging clinical, biological, and technical perspectives.
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Clinical Trial Manager, Class III Medical Devices BiibhrRemote, USA $117k–$117k3d Planning, coordination, and execution of clinical trials for Class III implantable medical devices to ensure safety, efficacy, and regulatory compliance.
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Global Clinical Operations (Multiple Roles and Locations) Industrial Placement, 2027 GskUK - Hertfordshire - Stevenage $26k–$26k3d Industrial placement roles supporting global clinical operations, study management, and clinical drug development for HIV medicines.
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Project Lead↗ Valis BioscienceRemote $75k–$75k3d Oversee clinical trial project planning and execution, coordinating team efforts and ensuring timelines and quality standards are met for pharmaceutical and academic clients.
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Lead Data Manager↗ ICON PlcBarcelona, CT, ES 3d Lead end-to-end clinical data management start-up activities from protocol review through database go-live, ensuring compliant study configuration and meaningful insights for strategic decisions.
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Lead Clinical Data Manager↗ Leica BiosystemsKA, IN 3d Lead clinical data management for pre-market and post-market trials in diagnostics, biotechnology, and life sciences, ensuring high-quality data execution and strategy.
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Solutions Design Specialist ClarioclinicalRemote 3d Deliver high-quality electronic Clinical Outcome Assessment (eCOA) solution designs for pharmaceutical and biotechnology clients by translating study protocols into optimized designs.
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Clinical Data Coordinator↗ Cognitive Research CorporationRemote, US 4d Supports Clinical Data Manager in delivering data management contracted services, focusing on database build, data review, and database closure.
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Senior Country Approval Specialist ThermofisherRemote, North Carolina, USA 4d Manage preparation, review, and coordination of local regulatory submissions (MoH, EC, gene therapy, viral safety) for clinical trials in alignment with global strategy.
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Clinical Data Lead (Data Manager) SanofiMorristown, NJ, US $122k–$122k4d Adapt and coordinate data management strategy for clinical studies to ensure data integrity and quality for statistical analysis and submission.
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Senior TMF Specialist↗ Arcus BiosciencesRemote $115k–$115k4d Collecting, reviewing, maintaining, and archiving essential Regulatory documents for the Trial Master File (TMF) to ensure inspection readiness and compliance with GCP and regulatory guidelines.
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Manager, External Data Management↗ Daiichi SankyoBasking Ridge, NJ, US 4d End-to-end delivery and quality assurance of external data (labs, biomarkers, companion diagnostics) for drug development and regulatory submissions.
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Sr. Manager, Medical Coding RegeneronHyderabad, IN 4d Lead and oversee medical coding activities for clinical development portfolios, ensuring accurate, consistent, and compliant coding of clinical data using MedDRA and WHODrug dictionaries.
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Data Specialist III LabcorpBengaluru India 4d Manage clinical study data transfer formats, protocol documentation, and end-to-end data lock processes for healthcare clients.
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Research and Education Data Manager↗ NSW HealthWestmead, NSW, AU $125k–$125k4d Manage, build, and optimize REDCap databases to transform clinical research and education data into trusted insights for Western Sydney Local Health District.
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Clinical Data Manager I CookchildrensFort Worth, TX, US 4d Manages all aspects of clinical data by interpreting, abstracting, and submitting accurate data relating to study subjects per study protocol and sponsor requirements.
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Senior Medical Writer/Principal Medical Writer PrecisionmedicinegroupRemote (UK) 4d Leading the development of high-quality, on-time clinical study documents including protocols, IBs, CSRs, and patient narratives in compliance with regulatory guidelines.
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