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...responsible for managing regulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 - Phase 4 spanning...Infectious Disease). The Regulatory Clinical Trial Application submission manager...
As QA Officer Clinical Products you provide QA support for clinical products received and distributed from the Breda site to clinical sites and depots. You'll be joining...
...maintaining follow-up correspondence; Processing and administering contributions (abstracts) submitted by the scientific/clinical community of reproductive/infertility specialists; Preparing the programme for publication on the Society&rsquo...
Manage end to end process for clinical site contracts and clinical trial related consulting agreements Support site-related questions regarding invoice preparation with...
...you will make sure all the right procedures are executed and applied. Profile : A master's degree in a scientific/clinical field, but a PhD or a post-doc is a plus At least 10 years of experience An impeccalbe knowledge of English You like...
...At least 7 years of experience as a Project Manager Cross functional experience in Pharma, IT, Finance, HR, R&D or Clinical environment Strong analytical and strategic background With hands-on approach Strong communication and change management...
...manufacturing, packaging, labeling and distribution of clinical trial material and auditor experience is a plus. You can...manufacturing, packaging, labeling and distribution of clinical trial material and auditor experience is a plus. You can...
...responsibilities are: Responsible for ensuring clinical trials are conducted in accordance...venipuncture, electrocardiograms, clinical, trials, sample, study, research...electrocardiograms is highly recommended and has a clinical sense to detect side effects Experience...
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