Clinical Research Associate

Cti Clinical Trial Services, Inc; São Paulo; Presencial; BRL 70.000 - 90.000; Tempo integral

Resumo da oferta

A global clinical research organization is seeking a Clinical Research Associate in São Paulo, Brazil. This role involves overseeing Phase I to IV studies, managing site activities, and ensuring compliance with regulatory guidelines. Candidates should possess a Bachelor's or Master's degree in health fields or be an RN with relevant qualifications. The organization promotes a supportive work culture with career progression opportunities and values employee education and work-life balance.

Serviços

Career progression opportunities

Tuition reimbursement

Flexible working schedules

Cash bonuses annually

Qualificações

• Bachelor's or Master's degree in allied health fields like nursing or pharmacy.
• RN with Associate's degree or 3-year nursing diploma plus 2 years of clinical experience.

Responsabilidades

• Manage investigative site activity for multiple protocols.
• Conduct study site visits and complete deliverables in the monitoring plan.
• Ensure proper storage and accountability of investigational products.

Conhecimentos

Clinical monitoring

Knowledge of drug development process

Good Clinical Practice (GCP)

Data integrity assurance

Formação académica

Bachelor’s or Master’s Degree in allied health fields

RN with Associate’s Degree

Descrição da oferta de emprego

Clinical Research Associate - São Paulo Brazil

(Level Depending on Experience)

Job Purpose / Summary

Completes project activities associated with monitoring functions of Phase I through Phase IV clinical research studies while continuing to develop knowledge of drug development process, ICH / Good Clinical Practice (GCP), and applicable local regulations.

Provides clinical and technical support for Clinical Research Associates (CRAs) and administrative staff.

Performs management of study site activities to ensure integrity of clinical data in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs).

What You’ll Do

• Manages investigative site activity for multiple protocols / indications and provides ongoing updates of site status to Study Manager / sponsor.
• Conducts study site visits (pre‑study, initiation, monitoring, and close‑out) and completes site visit deliverables within given timelines in the Monitoring Plan.
• Ensures proper storage, dispensation, and accountability of all investigational product(s) and trial‑related material.

What You Bring

• Bachelor’s or Master’s Degree in allied health fields, such as nursing, pharmacy, or health / natural science, or
• RN with Associate’s Degree or 3‑year Nursing Diploma with at least 2 years of clinical nursing experience

Why CTI?

• We support career progression - 25% of our global staff is promoted annually and we have a structured mentoring program to provide the support you need to move forward.
• We value education and training - We provide tuition reimbursement, partner with universities and colleges to create programs in our field, and have a dedicated training department.
• We value our people - We have never had a layoff in our 20‑year history, support a work‑life balance with flexible schedules, and have provided cash bonuses every year for the past decade.
• Our culture is unparalleled - Click here to learn more about "The CTI Way".
• We think globally and act locally - We have a global philanthropic program supporting our team's efforts to improve their local communities (Click here to learn more about our "CTI Cares" program).
• We are looking toward the future - We have had a consistent 15% growth rate over the last decade, invest in cutting‑edge technology, and pride ourselves on our average 95% annual retention rate.
• Our work makes a difference - We focus our work on treatments for chronically and critically‑ill patients, who are depending on us to bring these life‑changing therapies to market.