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Responsible for the oversight of clinical study execution in close collaboration with Clinical Operations lead, internal and external stakeholders (data management, biostatistics, programming, drug safety and PV, medical imaging, medical writing, research and discovery.
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Currently pursuing a BS/MS degree in biostatistics, statistics, or a related field. Keros Biometrics Department is in search of a highly motivated Biostatistician co-op to join our team. Proficiency in at least one statistical programming language (e.g. SAS, R.
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Working knowledge of drug development, clinical research, study design, biostatistics, pharmacokinetics, the regulatory environment, and medical terminology. Working knowledge of drug development, clinical research, study design, biostatistics, pharmacokinetics, the regulatory environment, and medical terminology.
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Biostatistics, Clinical research, statistics, sas, medical device. Collaborate with clinical operations team and head of biostatistics to develop objectives, design sampling, randomization, and statistical analysis plans to achieve study objectives.
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As a Sales Operations Analyst for Parexel you will be responsible for creating a competitive edge in winning projects for Parexel. As a Sales Operations Analyst for Parexel you will be responsible for creating a competitive edge in winning projects for Parexel.
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Working closely with other functional groups within Convatec's Clinical Operations team such as data analytics, site management, quality assurance and biostatistics where necessary to support milestone achievement and to manage study issues, resolve conflict and manage obstacles.
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Thorough knowledge of clinical medicine and clinical pharmacology and associated disciplines (e.g. biostatistics, data management, medical writing) The Medical Director, Clinical Development will collaborate with multidisciplinary functional representatives including Clinical Operations for study design and implementation, Pharmacovigilance, Regulatory Affairs, Medical Affairs, Biostats, Quality Assurance, Program management, Preclinical Development and other functions to ensure aligned design and execution of all programs.
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Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Non-clinical, Medical Affairs, Marketing, Legal, Quality, and other affiliates.
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Represent the THV Biostatistics department on all aspects of the clinical development process, ranging from clinical trial designs to regulatory submissions while applying scientific rigor to statistical methods and interpretation of results and also advise on the conduct of clinical studies, database development and data quality assurance with the analysis of clinical endpoints in mind.
$126,000 - $178,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Ensure clear and concise communication with operational and functional trial partners (e.g., Data Management Systems and Standards, Biostatistics, Trial Operations, Medical & Science, Clinical Supplies, Global Safety) including timely follow up.
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