- ICON Clinical Research (Boston, MA)
- …direction and decision-making processes, and offer expert medical and scientific guidance, leveraging therapeutic expertise to inform project development. **What ... and guidance on project teams. + Offering expert medical and scientific consultation throughout project lifecycles. + Ensuring compliance with ethical, legal,… more
- Takeda Pharmaceuticals (Boston, MA)
- …various key stakeholder functions (eg. Clinical, Clinical Operations, Medical Affairs , Commercial, Medical Writing) and represents Nonclinical and Translational ... + Partners with Clinical, Pharmaceutical Sciences, Computational Biology, Medical Affairs , Commercial, Business Development, and others to ensure that functional… more
- Orchard Therapeutics (Boston, MA)
- …on design of clinical development strategies and protocols that meet strategic, scientific and regulatory objectives of Orchard's clinical assets . Cultivate a ... collaboration with Clinical Operations, Data Management, Biostatistics, Regulatory, Medical Affairs , Pharmacovigilance and other teams supporting clinical development .… more
- Takeda Pharmaceuticals (Boston, MA)
- …the drug's value proposition will be recognized among the external ( scientific / payer influencing/HTA expert) stakeholder community and hence market access and ... Payer Marketing and Market Access, Global Evidence and Outcomes, Medica Affairs , Clinical Development, Regulatory Affairs , Biostatistics, Global Emerging Markets… more
- Bausch + Lomb (Boston, MA)
- …members, other B&L departments (eg, R&D/Project Management, Clinical/Medical Affairs , Biometrics, Regulatory Affairs , Quality Assurance, Pharmacovigilance/GPSS ... accurate and timely manner. + Provide Clinical Operations support to the Regulatory Affairs department. Leadership: + Manage in-house team of CRAs, CTAs and/or CTMs… more
- Bristol Myers Squibb (Cambridge, MA)
- …deadlines. **Education / Experience Requirements** + Bachelor's degree required; advanced scientific degree preferred (Masters, PhD, PharmD, BSN, etc.) with at least ... 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements**...globally for drug development and approval. + Understanding of scientific content and complexities and good knowledge of drug… more
- Astrix Technology (Boston, MA)
- …+ Ensure clinical initiatives are aligned with organizational goals and scientific advancements. + Design and direct early-phase clinical trials, including ... with cross-functional teams, including preclinical, clinical operations, and regulatory affairs , to integrate and execute clinical strategy. + Represent the… more
- AbbVie (Worcester, MA)
- …reliable and reproducible data in a timely manner. Read and adapt scientific literature to accomplish assignments and demonstrate broad and versatile technical ... then suggest, design, and pursue relevant experiments. + Understand relevant scientific literature and apply theoretical framework to solving problems within … more
- Sanofi Group (Cambridge, MA)
- …the authoring of the briefing document focused on the strategy and scientific content, leading the team through meeting preparations and moderating the meeting ... where relevant. **About You** **Qualifications:** + BS/BA degree in a relevant scientific discipline required. Advanced degree (PharmD, PhD, MD, or DVM or MSc… more
- Sanofi Group (Cambridge, MA)
- …Global Medical team, we are proud to support Sanofi's unrelenting commitment to scientific exploration and to work on a first-in-class treatment and robust pipeline ... industry compliance guidelines **About You** **Education:** Advanced degree in a scientific discipline (MD, PhD or PharmD) **Experience:** + Significant immunology… more
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