Director Companion Diagnostics Lead (all genders)
... .Proficient in writing and reviewing documents supporting regulatory submissions.Familiarity with ...
... .Proficient in writing and reviewing documents supporting regulatory submissions.Familiarity with ...
... up of clinical trial related documents and you’ll mange clinical biomarker ...
... of all regulatory relevant quality documents (e.g. MAA NDA, IMPD ...
... safety sections of various regulatory documents. You will provide expertise in ...
... projects in relevant regulatory submission documents (e.g. CTD 2.7. ...
... and approval of imaging trial document plans, imaging read schedules and ...
... to consider or return application documents sent by mail.
... and the production of technical documents and reports, is essential. Optional ...
... items.Generates and composes confidential, documents and materials and amend as ...
... consolidation of EGIB decision-making document to make a go no- ...