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The Senior Director will serve as the primary clinical pharmacology lead providing clinical pharmacology and bioanalytical expertise to the multidisciplinary project teams at Mural Oncology.
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Director, Clinical Data Management Solutions. Highly competent in clinical data management, various EDC systems, CDR systems, CDASH/CDISC standards, and medical coding dictionaries.
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Join us as a Director, Clinical Pathology in our Cambridge, MA location. The Bioanalytical and Biomarker Sciences and Technologies (BST) department at Takeda is seeking a strong scientific and strategic leader to join the group as a clinical pathology expert supporting pathology/IHC biomarkers in clinical development programs across therapeutic areas and modalities.
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Moderna is seeking a medical hematologist/oncologist with pharmaceutical experience (or M.D. with oncology drug development experience) to lead Clinical Development for one or more of their groundbreaking immuno-oncology-based development programs.
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Deep knowledge of immuno-oncology biology, biomarker strategies and application to clinical trials. Working with Research Unit biology leads and Precision Medicine Companion Diagnostic leads to ensure alignment of preclinical, clinical biomarker and CDx strategies.
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The Director, CPQP position resides within Alexion’s Clinical Pharmacology and Safety Sciences (CPSS) organization. The role represents the CPQP function on drug development teams, leads CPQP sub-teams, and owns strategy and delivery on posology for early and late-stage clinical trials while collaborating with clinicians, clinical operations, bioanalytical, biomarker, pharmacovigilance, regulatory and CMC groups.
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Dragonfly Therapeutics seeks a Director of Clinical Data Management to join our growing Data Management team within Clinical Operations. In addition to its wholly owned clinical assets, Dragonfly has a deep pipeline of wholly owned preclinical candidates discovered using its proprietary platform, as well as productive collaborations with Merck, AbbVie, Gilead and Bristol Myers Squibb in a broad range of disease areas.
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The Director, Bioanalytical Diagnostic Development, will be responsible for defining the global bioanalytical development strategy and leading all activities related to clinical bioassays/diagnostics, from preparations for ‘first in human’ up to registrational studies and post-approval commitments.
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Assisted Living Director (Clinical Care Coordinator) Want to know what makes our employees eager about going to work every day? Collaborates with Lifestyle Director on community-wide events / programs Assists with touring and providing information about our memory care program to families of perspective residents.
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The purpose of the Senior Director of Clinical Research role is to coordinate and lead the development of first in man (FIH), proof of mechanism (POM), proof of clinical activity (SoCA) and proof of concept (PoC) and dose ranging studies for novel biological and small molecule therapies in Immunology, Inflammation and Neurology focused programs.
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They will be at the intersection of study lab vendor, CRO and the broader clinical team to provide key expertise in study specific, potentially specialist, bioassay set-up and implementation. As a key member of the Clinical Development Team, they will ensure bioassay readiness requirements are achieved during study protocol design through to execution.
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Under the direction of the Senior Director, this position collaborates and regularly meets with key stakeholders, including Clinical Research Disease Center Managers, CTO Associate Directors of Regulatory Operations, Regulatory Affairs, Network and Satellite Program, Project Management / Monitoring and Education and Training to promote excellence and streamlined collaboration in clinical research across all disease groups.
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Collaborates with Lifestyle Director on community-wide events / programs. In collaboration with the Resident Service Director, provides a pre-admission screen assessment per MSL standards.
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The Senior Director, Clinical Data Management is accountable for the strategic leadership and functional management of all CDM deliverables in adherence to company SOPs and ICH/GCP. This role manages the CDM function, ensuring the development and readiness of personnel to deliver on existing programs while also being forward-looking and innovative.
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The Associate Director, Clinical Data Analyst, has a critical role in the delivery of high-quality external data across Dyne's development pipeline by proactively identifying, measuring, and mitigating risk prior to acquisition of non-electronic data capture (EDC) data.
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Title: director clinical Company: Chs Recruiting in Cambridge, MA
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