Actively contribute to innovation initiatives, including the evaluation of emerging technologies, process automation, and intelligent workflows within laboratory operations.
Challenge existing processes by proposing modern, scalable, and technology‑driven alternatives to traditional project set‑up models.
Lead or contribute to lessons‑learned sessions, translating insights into actionable recommendations and innovation roadmaps.
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Participate in the allocation of resources to clinical research projects by assigning staff to clinical studies based on their experience and training.
May support People Manager with the oversight of their staff, to ensure quality deliverables.
May identify quality risks and issues and support with the creation of appropriate corrective action plans to prevent or correct deficiencies in performance of staff.
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Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality.
Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks.
Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations.
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Qualitative studies: drafting discussion guide, prepare content analysis/ summary of IDIs, assist in qualitative report preparation, etc.
Be familiar with basic market research methodology/industry knowledge and take responsibility in overall project management with minimal support from project leader.
Well communication/coordination with supporting modules, such as FW, Data process, Quality control team to push projects moving smoothly.
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