CLINICAL RESEARCH ASSOCIATE I/II/III
Há 4 horas
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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