- Boehringer Ingelheim (Ridgefield, CT)
- …and consistency in all HCP engagements. + Partner with Legal to Review contract language and prepare standardized and routine alternative language responses to ... in all HCP engagements. + Partner with Legal to Review contract language and prepare standardized and routine alternative...experience. + Three to five (3-5) years in the pharmaceutical or healthcare related industry + Experience is preferred… more
- State of Colorado (Aurora, CO)
- …members. Accountable for ongoing evaluation and documentation of all components of pharmaceutical care delivered to residents. Train and mentor the activities of the ... fill for various facilities. This position performs day-to-day professional pharmaceutical operations of the department, which includes drug acquisition,… more
- Insight Global (Titusville, NJ)
- Job Description Insight Global's top pharmaceutical client is seeking a Omnichannel Lead to join their Omnichannel Marketing Strategy & Operations division. The ... teams across the Brands, Digital, Advanced Analytics, IT, creative agencies, MLR review , etc. This consultant will be responsible for working across functions and… more
- Genentech (South San Francisco, CA)
- …in the pharmaceutical industry. + You have knowledge of manufacturing data , QC data , computerized systems, laboratory testing and test methods, GMP ... makes us Roche. This role is based in the Pharmaceutical Technology SSF Quality Assurance division which is dedicated...role is a critical member of the Quality Product Review and Release (QPR&R) team. The QPR&R team spans… more
- Bayer (Whippany, NJ)
- …and maintenance of local labeling documents in accordance with the Company Core Data Sheet (CCDS) and associated documents for assigned Bayer Pharma products. In ... to the global corporate standards; + Leads the Labeling Review Team which is responsible for the development, ...(or equivalent experience) with a minimum of 8 years pharmaceutical industry experience (preferably within regulatory functions) or MS… more
- United Therapeutics (Research Triangle Park, NC)
- … data and insights for document development. Facilitate cross-functional review cycles and ensure timely delivery of high-quality documents. + Collaborate ... are as follows:** Who We Are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit… more
- AbbVie (North Chicago, IL)
- …applies sound medical judgment to effectively evaluate, interpret, and synthesize scientific data and translate into clear and concise safety summaries for inclusion ... of applicable regulations (eg, ICH, FDA, EMA, GCP) to lead authoring and review of assigned safety deliverables in accordance with standard operation procedures. +… more
- Mallinckrodt Pharmaceuticals (Webster Groves, MO)
- …methods, labels, etc ) + Facility/Equipment Qualification and validation (process/cleaning) + Stability data review / stability coordination + CAPA + Develop and ... engineer or equivalent role + Extensive experience in cGMP systems, pharmaceutical manufacturing and testing, experience must include role(s) in a manufacturing… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …of the managed care contract. Using critical thinking skills and data analytics, the incumbent will complete complex investigational audit reviews, identify ... spend your day** + Establish an audit plan to review the top 80% of contracted account formularies across...of contract terms and conditions + Advanced understanding of pharmaceutical rebate flow and decision points + 340B knowledge… more
- AbbVie (North Chicago, IL)
- …effectively conduct safety surveillance. * Responsible for safety surveillance for pharmaceutical / biological / drug -device combination products. * Lead, oversee, ... current regulatory guidance as appropriate. * Analyze and interpret aggregate safety data and communicate these analysis and interpretation to cross functional teams… more