- Stryker (Trenton, NJ)
- …focused on market access, or sustaining product portfolios. The position will require global clinical insight into launch strategies across multiple regions + ... data sources as an essential part of the clinical evidence generation strategy for Stryker's product portfolio. This...insurance claims databases + A basic understanding of the clinical evidence needs in the global regulatory… more
- Oracle (Jackson, MS)
- …Hugging Face Transformers, TensorFlow, or PyTorch. + Strong understanding of multi-modal data integration, clinical interoperability standards (FHIR, HL7), ... **Job Description** Oracle Health Data Intelligence (HDI) is at the forefront of...Oracle's AIDP platform to solve population health, research, and clinical interoperability challenges at global scale. +… more
- Otsuka America Pharmaceutical Inc. (Albany, NY)
- …Director, Medical Communications Lead, CNS Lead, and cross-functional teams (eg, Global Integrated Evidence & Innovation, Clinical Development, Regulatory, ... Manager of Core Content **Cross-Functional Collaboration** + Partner closely with Clinical Development, Global Integrated Evidence & Innovation, and Regulatory… more
- ThermoFisher Scientific (Greenville, NC)
- …as a senior regulatory leader responsible for shaping and executing the global clinical regulatory strategy across client's development portfolio. This role ... oversees end-to-end planning and delivery of global clinical submissions, leads the creation and release of core regulatory dossiers, drives country-level… more
- Takeda Pharmaceuticals (Boston, MA)
- …collaboration with stakeholders. + **Establish** **,** **maintain a** **nd govern** ** global standards , policies, and best practices** in biotherapeutic process ... collaborations, licensing, and strategic vendor relationships. + Establish and govern global standards and best practices, including technical guidance… more
- Merck (Rahway, NJ)
- …to be programmed, an understanding of statistical terminology and concepts. + Familiarity with clinical data management concepts + Experience in CDISC and ADaM ... **:** + Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and test study-level central monitoring analytics. + Map, manage, and design RBQM data flows to integrate with other relevant clinical and operational databases ... (eg, clinical development, site management, site monitoring, clinical operations, or data management) **OR** +...& Other Requirements** + Thorough knowledge of national and global regulations and guidelines governing clinical research… more
- Merck (North Wales, PA)
- …and programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data , transform the ... Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH +… more
- Sanofi Group (Cambridge, MA)
- …and clinical performance studies.Ability to synthesize and critically analyze data from multiple sources. + **Collaboration Skills:** Ability to work effectively ... information can be found through the LINK (https://benefits.sanofiusallwell.com/fleet/public/index/ba511bf8-5c32-4828-9861-ab985fffab90/?cid=sanofi) . Global Terms & Conditions and Data Privacy… more
- IQVIA (Durham, NC)
- …**Summary of the Essential Functions of the Job** + Cleaning and transforming raw clinical trial data from various sources to ensure accuracy and consistency for ... and tables to effectively communicate PK/PD findings. + Ensuring data is formatted according to CDISC standards ...master new techniques and technologies IQVIA is a leading global provider of clinical research services, commercial… more