
Senior Clinical Research Professional
Há 4 dias
This role presents a compelling opportunity for a skilled Clinical Research Associate to join our team in Brazil.
We are currently seeking an experienced professional to work on clinical research projects, ensuring compliance with study protocols and regulatory requirements.
Key Responsibilities:
- Monitor clinical sites to guarantee adherence to study protocols and regulatory standards.
- Collaborate with vendors to secure timely delivery of services.
- Conduct site initiation visits, monitoring visits, and close-out visits as required.
- Manage site documentation, including source documents and Case Report Forms (CRFs).
- Ensure the site is prepared for audits.
- Travel extensively throughout Brazil, potentially requiring air travel.
Requirements:
- Ability to work independently with minimal supervision.
- Strong communication and interpersonal skills.
- Excellent organizational and time management skills.
- Capacity to analyze data and identify trends.
What We Offer:
- A challenging and rewarding career opportunity in clinical research.
- Opportunities for growth and development.
- A collaborative and dynamic work environment.
How to Succeed:
- Demonstrate a strong understanding of clinical research principles and regulations.
- Showcase excellent communication and interpersonal skills.
- Display a high level of organization and time management skills.
- Demonstrate ability to analyze data and identify trends.
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