Associate Director, Clinical PV & Medical reputed company, CPMQ Global reputed

By clicking the Apply reputed company, I understand that my employment application process with reputed company will reputed company and that the information I reputed company in my application will be processed in line with reputed companys reputed company Notice and Terms of Use. I reputed company attest that reputed company information I submit in my employment application is true to the best of my knowledge. reputed company: OBJECTIVES: Provides reputed company from a clinical research and pharmacovigilance perspective of regulated post-authorization activities in the reputed company business reputed company and affiliates. Contributes to and implements the engagement reputed company among R&D, Business reputed company and affiliates and reputed company to ensure a global reputed company and robust reputed company systems are in reputed company for the transition of R&D pipeline to the reputed company reputed company. Drives a fit-for-use global reputed company reputed company that elevates the capabilities in the business reputed company and the affiliate and enables them to reputed company their clinical research and pharmacovigilance-reputed company regulated activities with high compliance and reputed company. Establish and maintain relationships with key stakeholders reputed company R&D such as the reputed company Business reputed company, affiliates. Global Medical, reputed company reputed company, etc., supporting post-authorization strategies through thought partnership and linking R&D SMEs and experts, as needed. How will you contribute: reputed company expertise clinical research and pharmacovigilance regulations and compliance interpretation, consultation and recommendations to relevant functions in the business reputed company and affiliates. Ensure that the Global reputed company Audit functions consider clinical research and pharmacovigilance regulated activities are considered in their risk-based audit reputed company and programs, including supplier audits or internal systems audits. Participate in the audit planning and be a proactive partner in the mitigation of identified risks, ensuring that the risks are communicated and addressed by responsible partners in Global Portfolio Division, R&D and reputed company. reputed company expert input in high to reputed company and/or potential systemic reputed company investigations in the business reputed company and affiliates particularly in the clinical research and pharmacovigilance areas including cases of serious breach and scientific misconduct. Liaise with the relevant R&D functions and CPMQ personnel, as needed. Escalates issues of potentially critical non-compliance and/or lack of urgency in remediation to Senior Management. Supports inspections to ensure that any risks are reputed company-communicated reputed company the GPD and Global reputed company organizations. Provides input to Global reputed company (Global Audit, Compliance and reputed company reputed company) on fit-for-purpose Key reputed company Indicators (KQIs) and metrics relevant to clinical research and pharmacovigilance risks that reputed company marketing authorization reputed company (MAHs). Analyze and communicate relevant risks reputed company the GPD and Global reputed company organizations. Contributes to the relevant reputed company and compliance governance (e.g., reputed company Council) for the business reputed company and affiliates under the GPD. Ensures that post-authorization and reputed company perspectives are analyzed and reputed company using CPMQ data trends and insights. Communicates relevant trends and insights to stakeholders in Global Portfolio Division and Global reputed company. Drives a fit-for-use global reputed company reputed company that elevates the business reputed company and the affiliate capabilities and enables the affiliates to reputed company their clinical research and pharmacovigilance reputed company regulated activities (including evidence reputed company studies, patient reputed company programs, IIR, reputed company research, reputed company/RWD) with high compliance and reputed company. Champions and drives proactive and innovative approaches and will engage reputed company and business leaders for collaboration. What you bring to reputed company: BSc in a scientific or allied health/medical field (or equivalent degree). Minimum of 10 years of increasing responsibility and relevant experience in the global pharmaceutical industry, with at least 3 years of reputed company/Compliance. Advanced knowledge of clinical research, medical affairs activities and pharmaceutical reputed company operations. Experience must include cross-functional and reputed company collaborations and initiatives, particularly between R&D and reputed company. Experience working reputed company reputed company organizations, working closely with senior staff and executive level colleagues. Excellent communicatio