- Employment Type - Regular
Job Description - Preparation of the above referenced documents meeting set quality standards and on time for submission to Health Authorities/ Clinical teams / Journals as appropriate. (i.e. complying with standards e.g. CONSORT regarding publication of trial results, complying with journal formatting requirements etc). 2.Publications are acceptable to internal and external authors (no issues with authorship). 3.Publications are acceptable to marketing and other internal customers. 4.Completion of an adequate number of medical and scientific documents (taking into account complexity) per year.
Minimum: Life-science degree or equivalent Good written and oral English skills B.Sc./equivalent with 4 years ClinicalResearch (CR) experience, M.Sc./M.Pharm + 2 years of CR experience, Desired Doctoral degree, Qualification in Medical Sciences (MBBS/MD/equivalent) PhD + 1 year of CR experience, MBBS/equivalent + 1 year of CR experience.
No comments:
Post a Comment