He has a comprehensive background of drug development and clinical operations with leading global pharmaceutical companies and CROs having drafted research protocols, development plans and medical reports; project managed studies in all phases; performed quality assurance audits; managed research staff and contractors; developed international clinical research conferences; lectured internationally and for academic institutions and advised regulatory agencies.
Services offered include:
Project management for Clinical Research
Medical writing: Development of study documentation for clinical research
Development and periodic updates of standard operating procedures portfolio.
Recruitment of key staff