Clinical Research Associate III
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Job Description
Clinical Research Associate III ensuring high-quality clinical trials in Brazil. Building partnerships and managing multiple study sites for Phase One to Phase Four trials.
Responsibilities:
- Build strong partnerships with clinical trial sites
- Serve as the primary point of contact throughout study delivery
- Manage assigned sites across Phase One to Phase Four trials
- Lead site initiation visits
- Conduct remote and on-site monitoring activities
- Evaluate site performance proactively and implement mitigation plans
- Drive early site engagement through feasibility activities
- Maintain complete and accurate study documentation
- Support inspection readiness through audit preparation
- Identify operational improvement opportunities
- Share expertise on complex trials and mentor colleagues.
Requirements:
- Bachelor’s degree in a scientific, healthcare, or related field
- At least five years of clinical research experience
- Strong knowledge of clinical trial processes and ICH and GCP guidelines
- Understanding of global regulatory expectations
- Demonstrated ability to manage multiple study sites independently
- Strong analytical thinking and risk-based decision-making skills
- Willingness and ability to travel approximately fifty percent.
Benefits:
- Health insurance
- retirement and wellbeing plans
- flexible working arrangements
- parental leave
- birthday day off
- employee recognition programs
- employee resource groups
- virtual self-development tools.
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