Services

All our English speaking professionals are self-employed and therefore highly motivated and organised, with at least 2 years of solid field-based experience. Without exception, all have considerable experience in feasibility, protocol translation, site management and monitoring of clinical Phase II-IV trials across a wide range of therapeutic areas. ICH GCP guidelines are strictly adhered to. Due to our excellent contacts with Ethics Committees and Regulatory Authorities study set-ups are expedited.

Geographical areas

Our Spanish network can provide your project
with CRAs, Auditors, site data managers and
protocol translators. We can also assist you
with referrals thoughout Europe.

Contracting local CRAs means less travel
costs, in-depth knowledge of local regulatory
requirements and good cultural awareness.

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