Senior Clinical Research Associate

PSI CRO; Costa Rica; Híbrido; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A leading clinical research organization is seeking a Senior CRA based in Brazil, Mato Grosso do Sul. You will be responsible for ensuring the compliance and Quality of clinical projects, building relationships with stakeholders, and conducting onsite monitoring visits. The ideal candidate will possess a degree in Life Sciences, with at least 5 years of monitoring experience, particularly in Oncology trials. This role offers both office-based and home-based work options.

Qualificações

• Minimum 5 years of independent on-site monitoring experience in the USA.
• Experience in monitoring Phase II and III clinical trials.
• Experience with complex Oncology trials (breast cancer) required.

Responsabilidades

• Conduct and report onsite monitoring visits.
• Be responsible for site communication and management.
• Supervise study activities and timelines.

Conhecimentos

Independent on‑site monitoring experience

Communication skills

Problem-solving skills

Ability to multitask

Ability to travel

Formação académica

College / University degree in Life Sciences

Ferramentas

MS Office applications

Descrição da oferta de emprego

Job Description

As a Senior CRA you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well‑being and quality of data compliance.

Office‑Based or Home‑based

You will :

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup (if applicable)
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Supervise study activities, timelines, and schedules on the country level
• Be a point of contact for in‑house support services and vendors
• Be involved in quality control, such as compliance monitoring and reports review
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions

Qualifications

• College / University degree in Life Sciences or an equivalent combination of education, training & experience
• Independent on‑site monitoring experience in USA (5 years minimum)
• Experience in all types of monitoring visits in Phase II and / or III
• Participation in clinical projects as a Lead / Senior Monitor
• Experience monitoring complex Oncology (breast cancer) trials required
• Full working proficiency in English
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem‑solving skills
• Ability to travel
• Valid driver’s license (if applicable)

Additional Information

Advance your career in clinical research and lead challenging full‑service projects on the country / regional level while growing with a company that puts its people first! You will get hands‑on involvement in every aspect of the study.

For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.