CLT

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.

 

Requisitos

Profile

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

 

Personal Profile

Time management, great communication, proactivity, and resilience.

 

Languages

Advanced English level.

 

Opportunity

São Paulo (remote)

Full-Time long term opportunity

 

Got Interested? Submit your CV to the Headhunter Juliana Stuzeneker (juliana.stuzeneker@venturatec.com) and schedule a confidential phone conversation for details!