Clinical Projects Assistant

**Summary**:The Clinical Supply Manager provides support for strategic planning, forecasting, and managing activities related to the procuring, packaging and distribution of clinical supplies that support Sponsored, Investigator Initiated, Expanded Access and Research Collaboration trials. They will participate in cross-functional teams which include our...

Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunit ies will present themselves, both professionally and personally. Join us, the future is ours to shape !**Major accountabilities**:-...

**Summary**:The Contracts Specialist provides contracting life cycle management support and business solutions optimizing operational expertise to Medical Affairs, partnering with all areas in the end-to-end planning process and execution.**About the Role**:**Key Responsibilities**:- Contract Life Cyle (CLC) Management: Performs contract management processes...

**Summary**:The Manager, Program Excellence - Data Management provides tactical support for the US Clinical Sciences line function organization within US Medical Affairs. Represents USMA to the Global project teams, aligns processes, tools and systems within USMA programs, and acts as the single point of contact for the relevant stakeholders in USMA. Should...

**Summary**:The Operations Manager, Informed Consent Form (ICF) Specialist will be the reviewer for business sections and responsible for adhering to USA legal/privacy requirements. The specialist will have full knowledge of consents as well as secondary responsibility executing study related agreements such as confidential agreement (CDA) for research...

**Summary**: Lead, support and report independent GCP/PV audits according to the NVS Quality Sys-tem and the current GCP/PV regulations to assess compliance with applicable regula-tions, standards, and guidance documents. Review and approve corrective action plans in support of the audit observations. Ensure alignment with strategic direction of the company...

**Summary**:**About the Role**:**Key Responsibilities**:- Manage and execute the medical review of all concepts/project plans, and protocols for the US-MA organization.- Support the development, update and presentation of training materials related to clinical trial process.- Assist with the oversight of revising/implementation of trial submission processes....

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies._ At AstraZeneca, we believe in the potential of our people and...

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies._At AstraZeneca, we believe in the potential of our people and...

**Summary**:- Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system. Assures procedures are in place...