environment by learning and adopting best practices. Follow and adhere to safety and security policies and procedures. Report immediately any safety or security issues or concerns. Your profile: Degree
statistical reports. Requirements: BSc or MSc degree in Biostatistics or related field and between 5-7 years’ relevant experience within the life-science industry, along with at least 1-year experience
suitable positions and projects. Supporting Pharmacovigilance activities including input to safety reports (local PSURs) Review and approval of promotional and non-promotional externally focused materials
suitable positions and projects. Supporting Pharmacovigilance activities including input to safety reports (local PSURs) Review and approval of promotional and non-promotional externally focused materials
ensure that target enrollment will be met across the allocated countries.Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory
Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.Collaborating with experts at study
plus.Minimum 5 years’ experience managing complex ER cases including investigations, ill-health, dismissals, appeals, and report writing.Experience of a fast-paced matrixed organization is helpful.Training
their clients, passionate about performance and commitment to a better future. Core Responsibilities The Assistant Facilities Manager (AFM), who reports into the EMEA SFM should be capable of managing
in business development activities for target clients and contribute to advancing JLL's market position in sustainability.Regularly report on progress to the Head of Sustainability - EMEA Markets Advisory and