CLINICAL RESEARCH ASSOCIATE I/II/III

Há 4 horas


São Paulo, Estado de São Paulo, Brasil RARASCRO Tempo inteiro

Company: RARAS CRO – The Fastest-Growing CRO in Latin America

About Us:

RARAS CRO is a leading clinical research organization in Latin America, known for its rapid growth and excellence in drug and medical device development from early-phase to phase IV. With a strong focus on quality, innovation, and scientific rigor, we are committed to advancing healthcare across and beyond our region.

Position Summary:

We are seeking experienced and self-driven Clinical Research Associates (CRAs level I/ II/III) to join our dynamic team in Brazil. This fully remote role offers the opportunity to work on impactful clinical trials with realistic metrics, full project oversight, and a strong focus on professional development and work-life balance.

Key Responsibilities:

  • Conduct site selection, initiation, monitoring, and close-out visits per GCP and protocol.
  • Support regulatory submissions and manage clinical trial documentation.
  • Oversee study supply logistics and liaise with vendors (e.g., depots, customs brokers).
  • Ensure data integrity through accurate monitoring and timely reporting.
  • Collaborate with investigators, site staff, and internal teams.
  • Review CRFs and source documents for accuracy and completeness.
  • Train and support site staff on study procedures and GCP.
  • Participate in investigator meetings and study-related activities.

Qualifications:

  • Bachelor’s degree in life sciences, nursing, or related field.
  • 2–6 years of CRA experience with a solid understanding of clinical trial operations.
  • Strong knowledge of GCP and local regulatory requirements.
  • Excellent communication, organizational, and problem-solving skills.
  • Proficiency in English and native Portuguese.
  • Ability to work independently and travel as needed.
  • Experience in rare disease studies is highly desirable.

What We Offer:

  • Competitive salary and benefits package.
  • Opportunities for career growth and cross-functional exposure.
  • Supportive, collaborative, and flexible work environment.


Rare Disease Experience is a plus.


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