Clinical Research Associate - All levels

ICON Strategic Solutions; Buenos Aires; Presencial; BRL 50.000 - 90.000; Tempo integral

Resumo da oferta

An established industry player seeks a Clinical Research Associate to ensure the integrity of clinical trials. In this role, you will monitor studies both onsite and remotely, verifying compliance with protocols and regulations. Your expertise will contribute to the protection of study participants and the accuracy of clinical data. This position offers an inclusive environment where your skills will be valued, and you will have the opportunity to train and mentor less experienced team members. If you are passionate about clinical research and looking for a dynamic workplace, this role is perfect for you.

Qualificações

• 3+ years of on-site monitoring experience, preferably in oncology.
• Fluency in English and Spanish is required.

Responsabilidades

• Monitor clinical studies ensuring compliance with protocols.
• Write reports on site findings and escalate issues as needed.

Conhecimentos

Clinical Monitoring

Data Integrity

Regulatory Compliance

Informed Consent Procedures

Report Writing

Training and Mentoring

Formação académica

Bachelor’s degree in health sciences

Descrição da oferta de emprego

Clinical Research Associate - All levels

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The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring trials are conducted, recorded, and reported in accordance with the protocol, SOPs, ICH-GCP, and all applicable regulations.

Main activities

1. Complete onsite and remote monitoring activities following ICH-GCP guidelines, regulations, SOPs, and study protocols.
2. Verify the protection of study participants by confirming informed consent procedures and protocol adherence.
3. Ensure the integrity of clinical data and compliance with the approved protocol, GCP, regulations, and SOPs.
4. Write and submit reports on investigational site findings and update tracking systems. Escalate issues and deficiencies with corrective and preventive actions as needed.
5. Participate in audit preparation and follow-up activities.
6. Potentially serve as a preceptor, training less experienced team members.

Requisites

1. Bachelor’s degree in health, life sciences, or medical fields.
2. Minimum 3 years of experience in on-site monitoring, preferably with oncology protocols.
3. Full availability to travel.
4. Fluent in English and Spanish (reading, writing, speaking).
5. Experienced candidates must be based in CABA.

What ICON Offers

At ICON, inclusion and belonging are core to our culture. We are committed to providing an inclusive, accessible environment for all candidates. We ensure a workplace free from discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.