and overall budget; Responsible for management of the Clinical CRO/Providers Acting as primary contact for Clinical (CRO) but also internal customers. Ensures adherence to scope of work within timelines and budget. Performs co-monitoring when needed, as...
solutions) comply with U.S., EU, and international regulations.
Reporting to the VP of Clinical Quality and Regulatory Affairs (CQRA), the role oversees all regulatory activities end‑to‑end: strategy definition, preparation of submissions (FDA 510(k), De...
Regional CRA – Oncology | Italy | Remote | FSP
We are supporting an advanced global FSP partnership with a US-based oncology biotech seeking an experienced Regional CRA to join a high-performing clinical operations team.
This is a remote-based...
and direction to a team of Field Medical Advisors / Medical Science Liaisons (MSLs) across key European markets. The role requires strong cross-functional collaboration with Global and Regional Medical Affairs, Clinical Development, Market Access, Commercial...
e.g., Study Monitoring Plan, Data Management Plans, CRFs, site training materials, Advertising Materials, etc.) as required. Oversee the work of CROs and other vendors (Central Labs, Clinical Supply Distributors, etc.) as assigned to clinical trials...
leads generated by the company.* You’ll create, monitor and revise lead generation plans to ensure a substantive sales opportunity pipeline.* You’ll inform customers of new product/service introductions and prices and you are internally giving input to...
works and overall budget; Responsible for management of the Clinical CRO/Providers Acting as primary contact for Clinical (CRO) but also internal customers. Ensures adherence to scope of work within timelines and budget. Performs co-monitoring when...
learning multimodal neural architectures
• design experiments, implement them in code, run them on large (GPU on HPC) compute, run evaluations
• monitor and benchmark the state of the art
• have the opportunity to give guidance to more junior team...
ER Services Sagl ER Services Sagl is seeking a Product Specialist on behalf of its client, a company specialized in Clinical Laboratory Information Systems, based in Ticino. The selected candidate will develop in-depth knowledge of the company's...
solutions) comply with U.S., EU, and international regulations.
Reporting to the VP of Clinical Quality and Regulatory Affairs (CQRA), the role oversees all regulatory activities end-to-end: strategy definition, preparation of submissions (FDA 510(k), De...
local/international regulations, including data protection legislation.
Conduct feasibility, site selection, initiation, monitoring, and close-out visits at investigational sites.
Collaborate with Regulatory Affairs and Clinical Operations teams on study...
HPC) compute, run evaluations
• monitor and benchmark the state of the art
• have the opportunity to give guidance to more junior team members such as PhD students and interns
• coordinate with our partners on our research roadmap
• adapt the project's...
and institutions. They provide information on research developments, and new concepts in medical treatment. The Medical Science Liaison will also participate in close partnership with Site Management & Monitoring staff in the initiation, oversight, and follow-up of...
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