- Genmab (Monmouth Junction, NJ)
- …authentic is essential to fulfilling our purpose. Associate Digital Product Manager, Global Drug Safety and Pharmacovigilance This person will be based out of ... and management of technology products in different focus areas in Global Drug Safety and Pharmacovigilance. These digital products are crucial to enable Business… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Team (SMT) materials- Supports overall program safety reporting (eg, Periodic Safety Update Reports (PSURs), Drug Safety Update Reports (DSURs), ... of protocol deviations- Discusses medical eligibility questions and answers safety questions (dose modifications, discontinuations, and management of adverse… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …generation, design and leadership of clinical development plans, and addressing all regulatory, drug and patient safety , data, CMC, IP, patient selection, market ... acumen.Providing best practices to DS's overall development strategy and drug development goals. Influencing their adoption and facilitating cross-functional… more
- Legend Biotech USA, Inc. (Baltimore, MD)
- …in a timely manner, submitting expenses, etc. Reports adverse events to Legend's Drug Safety department and other internal departments as appropriate per ... citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug -free workplace. more
- Taiho Oncology (TX)
- …responsibilities as defined in the pharmacovigilance SOPs related to medical inquiries and drug safety information. Use medical affairs plans to develop and ... align the tactical plan for MSL geography of responsibility and implement plans to support Medical Affairs strategic direction for assigned territory, eg medical territory plan Training/Education Resource: Develop, maintain and demonstrate scientific expertise… more
- Taiho Oncology (New York, NY)
- …responsibilities as defined in the pharmacovigilance SOPs related to medical inquiries and drug safety information. Uses medical affairs plans to develop and ... align the field tactical plan for MSL geography of responsibility and implement plans to support Medical Affairs strategic direction for assigned territory, eg, medical territory, engagement plans/ SL/HCP Rosters,. Training/Education Resource: Develops,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …a life sciences/pharmacy nursing degree with 13+ years' experience in global safety surveillance and/or clinical/ drug development Excellent verbal and written ... Position This leadership role is accountable for developing the safety strategy, major safety deliverables for assigned programs within the US East Coast… more
- Genmab (Skillman, NJ)
- …Oncology Clinical Devlopment. Responsibilities: Oversee clinical program including component studies Oversee safety of the drug , including the safety aspects ... of patients in clinical studies and signal detection with support of the Safety physician Lead and oversee creation of clinical components of key documents… more
- Merck & Co. (Durham, NC)
- …Durham, North Carolina. The new facility will include end-to-end processing of drug substances, drug products, including biotech culture growth, harvest, ... meet immediate business objectives even through adversity. This role will support drug product in regulated, clean room environments complying with current Good… more
- Catalent (PA)
- Account Director, Biologics Drug Substance Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative ... WI. This position has responsibility for establishing new biologics drug substance partnerships in the target territory. Success will...a difference. Catalent is committed to the health and safety of its employees, visitors and the customers and… more
- ALOIS Healthcare (Manchester, PA)
- …retail environment. Responds to customers questions about medications and advises about drug safety and potential interactions.ALOIS Healthcare Job ID #14357984. ... Pay package is based on 8 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Clinical Pharmacist:Retail,07:00:00-15:00:00About ALOIS HealthcareALOIS Healthcare provides top-quality… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders.Summary The Director, Clinical Safety , will be a product safety lead or part of a product ... safety team, and be responsible for overall product safety strategy or specific areas of safety ...to strategically manage benefit-risk throughout the lifecycle of the drug . Specific responsibilities will vary depending on the stage… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …for accelerated development and approval with smaller numbers of subjects exposed, Clinical Safety and Pharmacovigilance (CSPV) must be embedded in R&D as early as ... possible. This led us to create the Translational Patient Safety Senior Director position, which will have unique exposure to Daiichi Sankyo's global drug … more
- Aequor (Devers, TX)
- Top Must Have: Detailed experience with Contractor Safety , Safe Work Permit Program Support EHS training and Risk/Hazard Assessment Initiative/autonomy EHS audits ... EHS program implementation Job Description: Environmental, Health, and Safety Senior Specialist (EHS Senior Specialist) Onsite role--Local candidates only please… more
- Catalent (Emeryville, CA)
- …purification, and HPLC (high-performance liquid chromatography) analysis of site-specific antibody- drug conjugates (ADCs). The Research Associate II reports to the ... Solutions is the leading provider of pharmaceutical development services, drug delivery technologies, manufacturing, packaging, and product commercialization services… more
- Ace Hardware Corporation (West Jefferson, OH)
- …focus on this commitment. It is critical that all team members take responsibility for their safety as well as the safety of others to ensure that Ace Hardware ... is a world class safety organization. What you need...the USDOT (Part 391,Subpart E) Must pass pre-employment DOT drug screen. Must be "not prohibited" in the clearing… more
- Merck & Co. (Rahway, NJ)
- …characterization such that the process is scalable without compromising stability, safety , efficacy, and delivery. During development, we leverage smart experimental ... In summary, our team enables the translation of preclinical candidates into non-oral drug products. Our team is looking for a strong candidate for the position… more
- Catalent (St. Petersburg, FL)
- …timely development of new pharmaceutical products utilizing Softgel Formulation/Process drug delivery systems and technologies by carrying out required ... Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. The Role Responsible for… more
- Catalent (PA)
- …MO and Research Triangle Park, NC, as well as SMARTag Antibody Drug Conjugate technology in Emeryville, CA. Leveraging our growing differentiated technology ... and timeline of proposals for both new and ongoing drug substance programs and ensure scopes are adequately reviewed...through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. The… more
- Merck & Co. (Rahway, NJ)
- …single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.Primary activities include, but are not ... prepare our company's teams for meetings with FDA at any phase of drug development. Lead cross-functional efforts to prepare for advisory committees and may speak… more
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