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Senior Clinical Pharmacologist - Virology, Oncology, and/or Inflammation. Senior Clinical Pharmacologist - Virology, Oncology and/or Inflammation. These activities include, but are not limited to, collaboration on functional area activities during program implementation, clinical pharmacology study start-up/execution/close out, PK-PD and related analysis, interpretation and reporting, and support of regulatory filings.
$230,230 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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The Associate Director of Radiopharmaceutical Process Development will be executing the CMC development plan and IND enabling activities, leading to the clinical manufacturing of the Drug Product.
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Nonclinical Scientific Writer-BioanalyticsDo you want to be part of an inclusive team that works to develop innovative therapies for patients?
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With a combination-focused pipeline that exploits the power of six scientific platforms (Immuno-Oncology, Tumor Drivers and Resistance, DNA Damage Response, Antibody-drug Conjugates, Cell Therapy and Epigenetics) to help address unmet clinical needs in a host of hematological cancers, we are motivated by a dedication to the scientific discovery and collaboration that will one day help eliminate cancer as a cause of death.
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Behavioral Health, Mental Health, Licensed Clinical Social Worker, Licensed Marriage and Family Therapist, Licensed Professional Clinical Counselor, Clinical Leadership, Team Leader.
$136,029.34 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations. Protocol and ICF development process with minimal guidance; including writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality (collaboration with Medical Writing.
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Clinical expertise and technical proficiency in administering Travel X-Ray Tech. Clinical expertise and technical proficiency in administering Travel X-Ray Tech. Stay current with new techniques, technology, and medications related to X-Ray Tech practice.
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Quantitative Systems Pharmacology (QSP) & Physiologically Based Pharmacokinetics (PBPK) have become important components of discovery and clinical development. + Desire to interact as a modeling and simulation expert with matrix project teams and working closely with experts from different functional areas (pre-clinical and clinical and multiple therapeutic areas.
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AND or ASN (Associate Degree in Nursing/Associate of Science in Nursing Degree)BSN (Bachelor’s in Nursing) preferredCurrent Licensed Master Social Worker (LMSW)ASW (Associate Social Worker)Bachelor’s Degree in Social Work preferredLicensed Clinical Social Worker (LCSW) or MSW (Master’s Degree in Social Work) - years’ experience in clinical medical record auditing or equivalent role.
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To work collaboratively on multi-functional projects and interact with biomarker scientists and scientists from other functions including clinical pharmacology, biology, bioinformatics, clinical research, and clinical data science on a regular basis.
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Responsibilities: Responsibilities will include, but not limited to, the following:· To conduct statistical analysis from real-world observational or clinico-genomic data from Tempus and publicly available databases (e.g., TCGA, clinical trials, etc.
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Duration: 12 monthsLocation: South San Francisco, CAAs a Scientific Researcher I, you will be:Job Description:The Scientific Researcher performs laboratory-based activities and processes related to the tracking registration inventory preparation e.g. DNA/RNA extractions from human biospecimens fluid and tissue samples human cell culture organoid culture Serum Plasma and PBMC isolation from blood samples and distribution of biological samples from clinical and non-clinical trials.
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The incumbent will apply advanced data analysis skills and machine learning in collaboration with a group of computational and biological scientists to perform translational oncology research around multimodal translational data sets for programs in clinical development.
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The successful candidate will be an integral member of the DST research team and work closely with various Research functions such as medicinal chemistry, structural biology, and protein therapeutics to advance transformational therapies into clinical development for patients.
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Consider having with Project Data manager skillset with hands on designing experience of EDC-Veeva CDMS/Medidata RAVE databases for clinical studies. · Should have hands on experience in EDC-Veeva CDMS/Medidata RAVE clinical database & setting up EDC-Veeva CDMS/Medidata RAVE studies and program edit checks/dynamics per specifications and accountable for on time deliverables.
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clinical job Company: Biophase in Burlingame, CA
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