- Merck & Co. (Rahway, NJ)
- …site contact and site manager-throughout all phases of a clinical research study, taking responsibility of allocated sites.Develops strong site relationships and ... of the trial.Performs clinical study site management/monitoring activities in compliance with ICH-GCP,-Sponsor SOPs, Local Laws & Regulations, Protocol, Site… more
- Catalent (St. Petersburg, FL)
- Associate Scientist I, Analytical Research & Development Position SummaryCatalent is a global, high-growth, public company and a leading partner for the ... and analytical services to solve difficult development and manufacturing challenges.The Associate Scientist I, Analytical Research & Development supports… more
- Novo Nordisk Inc. (Los Angeles, CA)
- …The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific integrity; ... regulatory and process compliance ) for monitoring and site management activities. Takes ownership...and Novo Nordisk (eg, clinical trial site staff, clinical research vendors). Manages relationships with multiple internal stakeholders relevant… more
- Merck & Co. (Rahway, NJ)
- …Code of Conduct and the Ethics Ambassador Program, developing ethics and compliance training workshops and communications, and managing other key initiatives in ... candidate's ability to work effectively with colleagues within the Ethics and Compliance Office (ECO) and across divisions, functions, and regions. This position… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary This role ... support the leader in the development and implementation of the Compliance Monitoring Program, specifically Federal healthcare laws, FDA promotional guidelines, and… more
- Merck & Co. (North Wales, PA)
- Job DescriptionIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our renowned Research and Development division, ... drugs and vaccines for the benefit of patients and global human health. Our Research Scientists are our Inventors. We identify and target steps in disease mechanisms… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …business development goals through the successful negotiation and execution of research and strategic partnership contracting agreements. In collaboration with the ... Associate Director, the Associate Manager will support...with stakeholders across CMR to plan, negotiate and execute research and partnership projects that align with business objectives… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director, ESQL is responsible for all activities at the External Entity (EE) site associated with the manufacturing of company products ... to all applicable regulatory requirements, regulatory filings and company policies.The Associate Director also ensures that effective and robust Quality systems are… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionDescriptionThe Enabling Facilities (EF) group within the Chemical Engineering Research & Development (CERD) Department is seeking a highly motivated ... the Operations Specialist include the following:The Operations Specialist role at the Associate Specialist level will serve as a process team member supporting the… more
- Merck & Co. (Millsboro, DE)
- Job DescriptionPosition Description: Associate Director - Site Digital Technology Lead The Site Digital Technology Lead is the representative for Global Animal ... SDL (System Development Life Cycle) and CSV (Computer System Validation) compliance according to our Company guidelinesBrings together the right stakeholders to… more
- Merck & Co. (Durham, NC)
- …facility. As a direct report to the Director of Operations, the Associate Director will be accountable for the following: Support a comprehensive technology ... transfer of the HPV vaccine manufacturing process while ensuring compliance with all regulatory and safety guidelines. Lead a diverse team and be accountable for all… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary The ... Associate Director, Global Oncology Clinical Development (GOCD) Functional Excellence...training assignments to ensure accurate assignments are made and compliance with training goals are met. Ensures materials are… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.SummaryThe incumbent will be ... Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and execution at… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary The ... Associate Director Global Medical Affairs Oncology (GMA), under the...as scientific symposium and medical congresses, within legal and compliance regulations.Collaborates across functions to support GMA MI&E activities… more
- Merck & Co. (Boston, MA)
- Job DescriptionWe are seeking an experienced and innovative Associate Principal Scientist with a strong background in In Vitro Pharmacology to join the External ... of externalized In vitro projects across all discovery sites and our Research and Development Division's disease areas, as well as participate in relationship… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SummaryThe position holder ... direction and execute oversight of vendor delivery, to ensure compliance with the protocol, external/internal standards, applicable regulatory guidelines, policies,… more
- Merck & Co. (Durham, NC)
- …alignment with our incredibly high standards of quality. The Quality Assurance Associate Director will provide critical support in Teknika's continued efforts with ... assigned aspects of the incoming and operations process proceed in compliance with cGMP, applicable regulations, and our Company's Quality Management System.Focus… more
- Eisai, Inc (Nutley, NJ)
- …is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, ... in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of...your profile, we want to hear from you. The Associate Director, Omnichannel Marketing and Media position reports to… more
- Merck & Co. (Rahway, NJ)
- …the current IT division that provides support to the Pharmaceutical Research and Development (R&D), Supply Chain (Manufacturing), Marketing (Human Health) ... forecastStrong partnership and alignment with EIT Finance and IT PMOEnsure compliance with IT financial controls and standardsQualifications, Skills & Experience:… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary This position ... by managing labeling development or approval for either the US or EU.Ensure Compliance with Core Data Sheets/Label Changes: Manages updates to Core Data Sheets for… more
