- Takeda Pharmaceuticals (Boston, MA)
- …we do begins with our commitment to putting patients first. As a Director , Technology Business Partner for Global Development Operations, you will play a key ... solutions that support clinical trial operations, enhance data quality, and accelerate drug development - all while upholding Takeda's core values: Patient, Trust,… more
- Otsuka America Pharmaceutical Inc. (Little Rock, AR)
- …: Reporting to the Vice President, Global Medical Affairs, the Executive Director , CNS Strategy, Global Medical Affairs is a leadership position responsible for ... and advocates for Otsuka prominence in CNS space + Provides input into regulatory documents, including product labeling + Accountable for resourcing of personnel and… more
- GE HealthCare (Waukesha, WI)
- **Job Description Summary** Senior Director - PCS Services Technology is a key leader in the PCS Service team, responsible for engineering and innovation. This role ... Guide multi-generational technology strategies. + Ensure compliance with quality and regulatory standards. + Manage data and intellectual property strategy. + Mentor… more
- BeOne Medicines (Emeryville, CA)
- The Executive Director , Clinical Science will support BeOne Clinical and Medical assets by successful execution of clinical development programs and deliverables in ... in clinical development, program leadership, biometrics, clinical operations, safety/pharmacovigilance, regulatory , molecular diagnostics, and translational research. **Essential Functions of… more
- Abbott (St. Paul, MN)
- …products for treatment of vascular disease. Our extensive portfolio includes drug -eluting stents, bare metal stents, guide wires, balloon dilatation catheters, ... with global business objectives. + Collaborate with internal stakeholders ( Regulatory , Clinical, Quality, Operations, Marketing) and external partners (Key Opinion… more
- AbbVie (North Chicago, IL)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other program documents. + May oversee… more
- Abbott (Pleasanton, CA)
- …other regulatory requirements. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating ... closely with cross-functional peers in quality, operation, marketing, clinical and regulatory , medical affairs, commercials to define an aligned and predictable NPD… more
- AbbVie (Irvine, CA)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses and other program documents. *May oversee… more
- Takeda Pharmaceuticals (Boston, MA)
- …the Global Regulatory Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC. **How you will contribute:** + Plan, execute ... meetings, international experience preferred. + Understanding of scientific principles and regulatory CMC requirements relevant to global drug development and… more
- Wells Fargo (Portland, OR)
- …region + Develop and execute regional strategies aligned with legislative and regulatory priorities + Monitor, interpret, and assess the impact of public policy ... capacity + Experience identifying, tracking, and reporting on legislative and regulatory issues + Experience presenting information that persuades, and enhances… more