
Clinical Trial Specialist
Há 2 dias
We are seeking an experienced Senior Clinical Research Associate to conduct onsite monitoring visits in Brazil.
This role offers the opportunity to make a meaningful impact on the development of life-changing treatments for patients.
- Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites.
- Generate visit/contact reports and ensure compliance with standard operating procedures, protocols, GCP, and regulatory requirements.
- Build relationships with site staff to ensure rapport and promote integrity of the study.
- Develop patient recruitment strategies with clinical sites to meet enrollment timelines.
- Evaluate data quality and integrity, site efficacy, and drug accountability.
- Monitor completeness and quality of Regulatory Documentation and perform site document verification.
- Site Management or equivalent experience in clinical research.
- Understanding of clinical trials methodology and terminology.
- Ability to perform all clinical monitoring activities independently.
- Bachelor's or equivalent degree in biological science, pharmacy, or other health-related discipline.
- Strong interpersonal, written, and verbal communication skills within a matrixed team.
- Self-driven capacity, sense of urgency, and limited oversight.
- Client-focused approach to work and flexible attitude with respect to assignments/new learning.
- Honest and ethical work approach to promote treatment development.
- Strong computer skills, including CTMS, EDMS, MS-Office products like Excel and Word.
We offer opportunities for career growth, regular performance discussions, and evaluations. Our teams collaborate openly, share expertise, and promote learning.
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