- DAI (Bethesda, MD)
- **Senior Associate/Associate Specialist for the Head of USG** City/Country Location Details **Bethesda, Maryland** Employment Status Job Type **Corporate** **Job ... Title/Grade:** **Senior Associate/Associate Specialist for the Head of USG** **(P3/P4)** **Reports to: Chief of Staff, Office of the SVP** **Department: Technical… more
- AbbVie (Cambridge, MA)
- …and LinkedIn. Job Description The Senior Director Regulatory Affairs Therapeutic Area Head , GRS, is responsible for the management of global regulatory leads with ... marketed products. Key internal leader and driver of regulatory policy and strategy; ensures development of creative and impactful...least 2 regions in addition to the US (UK, EU , JAPAC, etc.) + NOTE: Higher education may compensate… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …pillar of Global Corporate Affairs (GCA) with responsibility for engaging global policy stakeholders to advance patient-centered policy solutions to accelerate ... with our local operating company (LOC) on key global policy topics. We are seeking an intellectually curious, team-oriented...Deep understanding of the role key governments (eg, US, EU , Japan) play in influencing the operating environment of… more
- Vanguard (Malvern, PA)
- …awareness of the investment industry, risk management practices, and regulatory and/or policy changes. Serves as a subject matter expert on risk management ... the division, firm, and industry. + Hires, evaluates, and supervises crew (US, EU , AUS). Provides guidance and training as necessary to develop crew. Sets… more
- Wayfair (Boston, MA)
- …for all destination operations Ensure effective coordination with Asia- and EU -based operations Enable effective inbound forecasting and planning for the Network ... with certain level of ambiguity An Important Note about Wayfair's In-Office Policy : All Boston-based interns, Co-ops, and corporate employees will be in office… more
- Olympus Corporation of the Americas (Westborough, MA)
- …The Global Lead of Respiratory Clinical Affairs reports directly to the Global Head of Clinical Research and collaborates closely with the leadership of Clinical ... includes all activities mandated by 21 CFR 812 or EU -MDR and GCP (ISO-14155:2020) and related to enrolling and...and operating planning activities in partnership with the Global Head of Clinical Affairs, in translating corporate and divisional… more
- Philips (Chicago, IL)
- …sales. + Develop and prepare product registration submissions for the US, Canada, EU , and support submission preparation for all regulated markets. + Review and ... maintain quality and regulatory compliance. + Reporting to the Head of Regulatory Affairs for AM&D, you will communicate...preparation and submission of 510K's, PMA's and experience with EU MDR/MDD, Health Canada, China, etc. + You have… more
- Santander US (Boston, MA)
- …risks. An excellent understanding of the evolving regulatory landscape in the US and EU are vital for success in this role. The day-to-day focus may vary depending ... of the overall second line of defense program priorities directed by the Head of Technology Risk and may include: planned or ad-hoc technical risk reviews,… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …to Life.** **Job Description** Serves as a principal assistant to the Global Head of Legal - Regulatory, Quality, Medical & Scientific Affairs. Responsible for ... for all business units, worldwide, delegated by the Global Head of Legal - Regulatory, Quality, Medical & Scientific...etc.): Position is remote, with expected travel to Japan, EU and China approximately 5 -15%. **Preferred:** + Must… more
- Chiesi (Cary, NC)
- …applicable to supported regions or areas of responsibility. + With guidance from Unit Head , assist in the identification of the EU and US regulatory requirements ... or areas of responsibility + With guidance from Unit Head , assist in the preparation and presentation of regulatory...basis protected by local, state or federal law. This policy applies with regard to all aspects of one's… more
- Olympus Corporation of the Americas (Westborough, MA)
- …The Executive Director of Global Clinical Operations reports directly to the Global Head of Clinical Research and collaborates closely with the MSA leadership team ... 5-year time horizon, and is accountable to the Global Head of Clinical Affairs. + Other duties as assigned....global regulations, guidelines and standards (ie, ICH E6 (R2), EU MDR, ISO 14155:2020) and good document management practices.… more
- Merck (Rahway, NJ)
- **Job Description** Reporting directly to the Head of Global Investigations in our OGC (Office of General Counsel) organization, the **Director, Global ... must have ability to work/support as per **LATAM and EU Time Zones.** + This role could be based...Spanish. **NOTICE FOR INTERNAL APPLICANTS** In accordance with Managers' Policy - Job Posting and Employee Placement, all employees… more
- Citigroup (Tampa, FL)
- …ACRM Global Funds Transfer Vice President reports directly to the Global Head of Funds Transfer Compliance. **Responsibilities:** + Support the development and ... Standards/Payment Transparency/specific funds transfer regulations (for example, US Travel Rule, EU FTR, etc.). + Where necessary, provide credible challenge to… more
- Gap Inc. (San Francisco, CA)
- …numerous projects and complex matters simultaneously under deadline pressure + Support Head of Commercial Contracts Legal as appropriate in the evolution of our ... products, privacy experience (with knowledge of US state and UK/ EU privacy laws, Generative AI, and AdTech) a plus....to Gap Inc.'s face mask and proof of vaccination policy as said policy is no longer… more
- AbbVie (South San Francisco, CA)
- …that corporate goals are met. Key internal leader and driver of regulatory policy and strategy for assigned products. + Leads preparation of global regulatory ... the direction of a GRS Sr GRL or TA Head . May participate in or lead regulatory and Company...major regions in addition to the US, such as EU or Japan. Strong global drug development foundation with… more
- Takeda Pharmaceuticals (Boston, MA)
- …Regulatory Affairs CMC team, you will report to the Executive Director and Head , CMC Regulatory Affairs - Pharmaceuticals. **How you will contribute:** + Leads the ... setting processes of major regulatory agencies (eg US FDA, EU , PMDA, NMPA, WHO). + Actively engaged in major..."hybrid" in accordance with Takeda's Hybrid and Remote Work policy . \#LI-RM1 **Takeda Compensation and Benefits Summary** We understand… more
- Takeda Pharmaceuticals (Boston, MA)
- …& Pharmacovigilance (PSPV) team, you will report to the Director and Head , PV Document Management (PVDM). **How you will** **contribute:** + Provides leadership ... business, including drug development and regulatory aspects. + Knowledge of US, EU and international regulatory/safety regulations and guidelines. + Fluency in oral… more
- New York University (New York, NY)
- …to gain research experience with multiple methods (motion recording, head -mounted eye tracking, computerized video coding, psychophysical procedures) and to ... the position has been filled. For people in the EU , click here for information on your privacy rights...an Equal Opportunity Employer and is committed to a policy of equal treatment and opportunity in every aspect… more
- New York University (New York, NY)
- …with multiple methods (computerized video coding, high-speed motion tracking, head -mounted and remote eye tracking, instrumented gait carpet, EEG, psychophysical ... Interfolio as soon as possible. For people in the EU , click here for information on your privacy rights...an Equal Opportunity Employer and is committed to a policy of equal treatment and opportunity in every aspect… more