Design of research strategies for pharmaceutical companies and academia taking into account the regulatory framework.
Vast and diverse experience in producing and reviewing scientific documentation in the field of medical sciences: Observational studies and Clinical Trials Protocols, Clinical Study Reports, Research Articles.
Strong leadership and motivational skills and a large experience in working with collaborative and multidisciplinary groups.
Excellent written and oral communication skills and very detail-oriented.
10-year experience in working in clinical trials operational environment (CRA and project manager)
Areas of expertise: biologics, post-authorisation and outcomes research, patient-centered outcomes, pharmacoepidemiology and drug utilization research.
Medical Writing Manager, Eurotrials, Scientific Consultants2 Jan 1998 → …
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