... relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession Good knowledge of clinical trials, combined with in-depth knowledge ...
... contributing to and learning from global clinical investigation submission and strategy experiences. ... 1, and other national or global regulations related to clinical investigations. You have strong time ...
... contributing to and learning from global clinical investigation submission and strategy experiences. ... 1, and other national or global regulations related to clinical investigations. You have strong time ...
... supporting the execution of our Global Litigation & Dispute Resolution strategy across ... supporting the execution of our Global Litigation & Dispute Resolution strategy across ... insight, which combines the firm’s global standards with in-depth local ...
... will compile, publish and produce Clinical Trial Authorization Applications and associated CTA ... to the regulatory aspects of clinical trials are tracked in the company- ... that is one of the global med-tech leaders (sponsor) Attractive ...
... will compile, publish and produce Clinical Trial Authorization Applications and associated CTA ... to the regulatory aspects of clinical trials are tracked in the company- ... that is one of the global med-tech leaders (sponsor) Attractive ...
... will compile, publish and produce Clinical Trial Authorization Applications and associated CTA ... to the regulatory aspects of clinical trials are tracked in the company- ... that is one of the global med-tech leaders (sponsor) Attractive ...
... the services needed to perform clinical trials of new medicines. Our work ... in Poland You will: Analyze clinical trial protocols and translate requirements to ...
... (eTMF, CTMS, SSU, Payments) for clinical trial management from site selection to ... Sciences industry with exposure to Clinical Trials and affinity to technology. Experience ...
... will compile, publish and produce Clinical Trial Authorization Applications and associated CTA ... to the regulatory aspects of clinical trials are tracked in the company- ... that is one of the global med-tech leaders (sponsor)Attractive ...