Our client is a Boutique CRO with 20+ years of market experience, headquartered in Brazil, and a presence in Latin America.
We are recruiting Regulatory (start up) Analysts for Clinical Trials – All levels (I, II e SR). The professional must be experienced with submission to Ethics committees and MOH (Ministry of Health) for Phase I, II, III, IV, observational studies, and post-trial/ compassionate use programs.
You enjoy participating in the decisions in a company with an agile culture. You will receive training, enjoy the flexibility of remote work, and the possibility to collaborate in a fast-paced growth environment (we had cases where a professional was promoted 3x last year). Check the details below and schedule a phone conversation.
1-6 years of experience with start-up and maintenance of regulatory activities for clinical Trials
Submission to Ethics committees and MOH (Ministry of Health) for Phase I, II, III, IV, observational studies and post-trial/ compassionate use programs
Follow up importation and exportation of medication and supplies (logistics)
Support the Regulatory Manager in the regulatory strategies
Must have fluent English ( speaking, written, listening, and reading)
Experience working in the pharmaceutical industry or CRO required
Time management, great communication, proactivity, and resilience.
Advanced English level.
São Paulo (remote)
Full-Time long term opportunity
Got Interested? Submit your CV to the Headhunter Juliana Stuzeneker (firstname.lastname@example.org) and schedule a confidential phone conversation for details!
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