) VEEVA RIM Expert User GRA: o Coordinate all user activities regarding the tracking of regulatory events in relation with clinical trials & all global and local disclosure activities Act as GRA window
challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment
/statistical reports, integrated summaries and/or NDA sections • Leading studies at an operational level • Provide expert review and initiate methodology development work with
) VEEVA RIM Expert User GRA: o Coordinate all user activities regarding the tracking of regulatory events in relation with clinical trials & all global and local disclosure activities Act as GRA window
challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment
EMEA level. Role & Responsibilities Be an expert in facilitating IQVIA’s real-world patient data to answer commercial business objectives from pharma clients with a focus on HQ and multi country
– Planning & Assurance, you can anticipate some of your day-to-day tasks to include: Lead a team of seven (7) Project Quality Engineers through the ramp-up and delivery of multiple programs Provide expert
– Planning & Assurance, you can anticipate some of your day-to-day tasks to include: Lead a team of seven (7) Project Quality Engineers through the ramp-up and delivery of multiple programs Provide expert
information on the portfolio, answering questions from healthcare clinicians and disease experts regarding product safety or efficacy that is not addressed in a product’s label and supporting research
memorable human experiences for the client, the internal JLL team, and the account’s OneTeam while upholding safety standards.You are a passionate expert that embodies the JLL Human Experience culture of