- Stanford Health Care (Palo Alto, CA)
- …FDA drug recalls, drug information, special programs, sample medications, investigational studies , and other related medications. + Coordinates with pharmacist and ... pharmacy technicians to develop and maintain standard work and operating procedures. **Education Qualifications** + PharmD Degree from an accredited college/university required. **Experience Qualifications** + Five (5) years of progressively responsible and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Support the rollout and maintenance of standardized macros across studies and therapeutic areas.Key Tasks: Understand the macro classification (Core, ... process and version control checklist. Summary matrix linking macros to study usage and version history. Qualifications: Education: Currently pursuing a master's… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …function as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, US and Global Brand Team, and US Product ... Team to inform clinical development, commercialization, market access, and other cross-functional strategic...USOMA teams as part of evidence generation forums and study teams for Local/Regional Medical Affairs company sponsored … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …critical evidence and educational gaps through targeted strategies (eg, scientific education, clinical studies ) to advance biomarker and CDx understanding and ... within Global Oncology Medical Affairs, Regional Medical Affairs, Precision Medicine, Clinical Development, RWE/HEOR, Discovery and Business Development as well as… more
- Formation Bio (New York, NY)
- …and CSV activities across various entities, investigator sites, research organizations, clinical and nonclinical studies , PV vendors, and CDMOs. Maintain ... potential quality risks. Managing quality-related activities related to manufacturing, clinical trials, and nonclinical studies , including conducting audits… more
- Novo Nordisk Inc. (Irvine, CA)
- …improved patient health Demonstrates thorough knowledge of all promoted NNI approved clinical studies and the skill to engage customers (prescribers, support ... Sales Representative also assists their target physicians with their local clinical and educational initiatives by coordinating company resources (eg, counterparts,… more
- Caris Life Sciences (Tempe, AZ)
- …+ Provide clinical study site oversight. + Real-time escalation of clinical studies risks and issues to management. + Create and maintain trial master ... appropriate cross-functional teams. The Global Companion Diagnostics Specialist will support clinical study compliance through creation and maintenance of trial… more
- Parexel (Tallahassee, FL)
- …assigned project/ study . + Participate in the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), ... Supporting Activities - Medical Support / Medical Monitoring for projects and studies contracted to Parexel - Deliver all medical support required for successful… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …function as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, US and Global Brand Team, and US Product ... Team to inform clinical development, commercialization, market access, and other cross-functional strategic...USMA teams as part of evidence generation forums and study teams for Local/Regional Medical Affairs company sponsored … more
