- Eisai, Inc (Nutley, NJ)
- … clinical and research insights from KOLs to Medical Affairs . Training/Education Resource Maintain and demonstrate thorough and up-to-date knowledge of ... Sr. MSL) is a field-facing representative of US Medical Affairs with a primary responsibility of engaging in the...and its hhc mission; b) provide key scientific and clinical information about Eisai's products/pipeline; serve as a conduit… more
- Eisai, Inc (Boston, MA)
- …or Principal Medical Science Liaison) is a field-facing representative of US Medical Affairs with a primary responsibility of engaging in the exchange of scientific ... information about Eisai, the company and it's hhc mission, and key scientific/ clinical information about Eisai's products, demonstrating a pattern of good judgment,… more
- Eisai, Inc (Provo, UT)
- …or Principal Medical Science Liaison) is a field-facing representative of US Medical Affairs with a primary responsibility of engaging in the exchange of scientific ... information about Eisai, the company and it's hhc mission, and key scientific/ clinical information about Eisai's products, demonstrating a pattern of good judgment,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …QA oversight.Drive innovative process improvements across RD, PV, and Medical Affairs by leveraging emerging technologies and industry best practices.Ability to ... line functions. Set the strategic direction to define best approach for clinical development systems, PV systems and MA systems including data management,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and compliant with relevant regulations. This role will work with Global Regulatory Affairs and cross-functional teams (eg, Quality, CSPV, Clinical Operations, ... Process Manager will be a key member of the Global Regulatory Affairs (GRA) Process Excellence & Analytics function, responsible for ensuring Daiichi Sankyo's… more
- Genmab (NJ)
- …Director, External Data Quality Management, is a strategic leadership role within Clinical Data Management. This individual is accountable for driving the strategy, ... quality, and integrity of external data across the clinical trial portfolio. This role serves as a Subject Matter Expert (SME) in protocol quality, central and local… more
- Eisai, Inc (Raleigh, NC)
- …the Director will oversee Global Logistics and Import/Export compliance for commercial, clinical , and research materials. This includes the Eisai Customs and Border ... the Director will oversee Global Logistics and Import/Export compliance for commercial, clinical , and research materials. This includes the Eisai Customs and Border… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …TA & other TAs, cross-functional teams, including sales, marketing, medical affairs , market access and policy/advocacy (MAPA), Centers of Excellence (COEs), ... regulatory affairs , and other relevant NNI departments to ensure alignment...Proven knowledge of the pharmaceutical industry, including medical, regulatory, clinical processes and market dynamics, especially within identified therapy… more
- Genmab (NJ)
- …with key stakeholders within Global Development Operations (GDO), Medical Affairs , Medical, and/or CROs, to enable expedited, predictive delivery for ... competitive landscape) that represent operational risks for the execution of clinical trials within the given indication/program.Key contributor to the study's… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …ensure successful implementation of the CDx and associated data collection. Oversees clinical trial sample testing activities and data capture to support CDx ... the Dx partner for CDx project contracts. Supports CDx analytical and clinical validation studies in collaboration with Dx-partner Provides scientific and technical… more
