Clinical Research Professional with Expertise in Monitoring
hace 3 semanas
We are seeking a skilled and experienced Clinical Research Associate to join our team as a freelancer. This is a temporary position based in Argentina, requiring full working proficiency in English and Spanish.
About the Job:
The successful candidate will conduct onsite monitoring visits, review clinical trial records, verify source documents, and resolve queries. They will also be responsible for site communication, management, and collaboration with internal project teams. Additionally, they will participate in feasibility research and support the regulatory team in preparing study submissions.
Key Responsibilities:
- Conduct and report onsite monitoring visits, including Phase II and III studies
- Review and verify clinical trial records, ensuring accuracy and completeness
- Communicate effectively with sites, stakeholders, and internal teams
- Participate in feasibility research and provide recommendations
- Support the regulatory team in preparing study submissions
Requirements:
- College/University degree in Life Sciences or equivalent combination of education and experience
- At least 2 years of independent onsite monitoring experience in Argentina
- Experience in all types of monitoring visits in Phase II and III studies
- Availability to travel domestically and internationally
- Full working proficiency in English and Spanish (written and spoken)
- PC skills, including Microsoft Office Suite (Word, Excel, PowerPoint)
- Strong problem-solving, communication, and teamwork skills
What We Offer:
- A competitive salary of $60,000 - $80,000 per year, depending on experience
- A dynamic and supportive work environment
- Opportunities for professional growth and development
- A chance to work on challenging projects and contribute to the success of our company
How to Apply:
Please submit your CV and cover letter to us via email. We look forward to hearing from you
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