, and conducting analyses. Context of the Role The Regulatory Affairs Manager will join the Innovative Trials Hub and will take the.... Their significant expertise in regulatory affairs within clinical trials is essential for navigating the complex global regulatory...
Manager (CSM) to oversee and drive the execution of clinical trials for our innovative cell and gene therapy programs. The... with cross-functional teams, including clinical operations, regulatory affairs, quality assurance, and medical affairs, to drive...
Job Title: Medical Affairs Advisor/Manager - Rare Disease Job Location: London, UK Job Location Type: Remote... Job Contract Type: Full-time Job Seniority Level: Mid-Senior level Rare Disease Medical Affairs Advisor/Manager...
, regulatory) preferred Advanced understanding of pharmaceutical development, clinical trials, analysis and interpretation...Job Description Summary 1,800+ associates. 86 countries. One Regulatory Affairs. At Novartis your voice, experience...
safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor Train new Clinical Safety Coordinators... data entry, tracking of pending cases, collaborate with Medical Monitor and Regulatory Affairs) Qualifications...
safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor Train new Clinical Safety Coordinators... data entry, tracking of pending cases, collaborate with Medical Monitor and Regulatory Affairs) Qualifications...
safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor Train new Clinical Safety Coordinators... data entry, tracking of pending cases, collaborate with Medical Monitor and Regulatory Affairs) Qualifications...
Writing & Submissions, Regulatory Affairs, Trial Management, etc.) on the planning, preparation, and delivery of high-quality... Desired Budget Management, Clinical Trials, Negotiation Skills, People Management, Process Improvement, Project Planning...
and regulatory requirements. Cluster oversight: Acts as operational manager of the CPSH’s/CPSH associates in the cluster. The..., etc.). Health Authority Requests: In collaboration with Regulatory Affairs (RA), ensure processes are in place to answer fully...
from clinical trials and the real world to generate fit-for-purpose evidence that is applied to decision making in drug development...). More than 3 years experience in clinical drug development with extensive exposure to clinical trials. Strong knowledge...
from clinical trials and the real world to generate fit-for-purpose evidence that is applied to decision making in drug development...). · More than 3 years experience in clinical drug development with extensive exposure to clinical trials. · Strong knowledge...