- Lundbeck (Deerfield, IL)
- …you can directly see the results of your hard work? Lundbeck is a global biopharmaceutical company focusing exclusively on brain health. With more than 70 years of ... efforts to differentiate and expand access to treatment, working closely with global colleagues to support the design, protocol review and execution of Phase… more
- Medtronic (North Haven, CT)
- …and Supplier Change Requests, for the Core Suture portfolio. Analyze and monitor global and local regulations and standards applicable to medical products, ... CT. Responsible for developing strategies for worldwide product registration with global regulatory agencies to introduce Wound Management devices to market,… more
- Gilead Sciences, Inc. (Foster City, CA)
- … level. The Real-World Evidence (RWE) function at Gilead is part of the Clinical Data Sciences (CDS) group within the Development organization and aims to ... unlock the power of Real-World Data (RWD) to help transform innovations to life-changing medicines...CDS (eg, Biostatistics, Bioinformatics), as well as partners in Clinical Development, Global Patient Safety, Regulatory Affairs,… more
- IQVIA (Durham, NC)
- …major incidents, including root cause analysis and resolution planning. + Translate Global Network Support (GNS) standards into actionable low-level designs, ... and/or Linux certifications preferred but not required IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- Gilead Sciences, Inc. (Foster City, CA)
- …including Clinical Development, Clinical Operations, Regulatory, Safety, and Clinical Data Sciences. + Identify and drive continuous quality process ... + Lead the analysis and interpretation of key quality data in Program/Study Quality Briefs for the presentation and...an expert and provide guidance on and interpretation of global GCP regulations and Gilead standards for… more
- Genentech (South San Francisco, CA)
- …Drive the design, execution, and monitoring of high-quality Phase IIIb/IV clinical trials, investigator-initiated research, and health economic data analysis ... product support including collaboration with the relevant stakeholders to drive timely data generation and dissemination. They are expected to maintain an in-depth… more
- Genentech (South San Francisco, CA)
- … data for regulatory approvals, payer negotiations, and inclusive research standards , aiming for faster clinical trial enrollment and increased participation ... in external collaborations and evidence generation, ensuring alignment with Roche standards , legal frameworks, and evolving global regulatory expectations.… more
- Oracle (Lansing, MI)
- …and save lives. Our mission? To create a human-centric healthcare experience powered by unified global data . It's a big challenge, but big challenges are what we ... leaders, end users, and technical teams. + Ability to analyze healthcare data , integrate industry standards , and translate insights into actionable… more
- Candela Corporation (MA)
- …MBA (preferred) 2.5+ years in product marketing with 2+ years with global responsibility **Essential Job Requirements: (Mandatory for Clinical and Regulatory ... messaging, shaping go-to-market strategies, and ensuring commercial readiness across global markets. Responsibilities also include enabling sales teams, generating… more
- Lundbeck (Deerfield, IL)
- …you can directly see the results of your hard work? Lundbeck is a global biopharmaceutical company focusing exclusively on brain health. With more than 70 years of ... and execute in partnership with internal stakeholders such as Clinical , economics and outcomes, and real-world evidence teams to...plan for research projects. + Provide US perspectives to Global teams on evidence strategy and needs. + Provide… more