Das ist der Job
Responsibilities Provide strong, independent leadership for assigned clinical projects, ensuring successful execution.
Darum lohnt es sich
Provide mentorship and guidance to junior project team members. Participate in internal and external project team meetings to ensure alignment and success. Serve as the primary point of contact for clients, vendors, and internal stakeholders. Oversee study management activities, including site selection, initiation, monitoring, and closeout.
Develop and maintain study timelines, budgets, and project plans, ensuring adherence to scope. Mitigate risks and proactively address challenges to keep projects on track. Ensure compliance with ICH-GCP, regulatory guidelines, and company SOPs. Manage vendor relationships and study‑specific contracts.
Support proposal development, bid defense meetings, and business growth initiatives.
Requirements Bachelor’s or Masters degree in a science or related field Previous experience working on clinical projects within an academic, CRO or pharmaceutical company environment Experience in Renal is mandatory Relevant work experience recommended for this role includes approximately seven (7) years of industry experience.
A minimum of two (2) years of Project Management experience within the CRO industry is mandatory. Prior experience as a CRA, in site management, trial coordination, or other relevant industry experience is preferred.
Experience managing single or different regions, working across different therapeutic indications, managing full-service studies, worked across early phase to Late phases of clinical trial, is preference Excellent working knowledge of, and ability to implement project activities in accordance with, ICH/GCP and all applicable regulations and guidelines in the relevant regions.
Previous exposure to client-facing interactions and/or client management Project finance management experience, CRO preferred. #J-18808-Ljbffr
