CRA II and SR CRA

ICON Clinical Research; São Paulo; Presencial; BRL 90 000 - 150 000; Tempo integral

Resumo da oferta

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a CRA at ICON, you will contribute to our clinical trial operations function, delivering high-quality monitoring remotely from Brazil, coordinating study activities, and maintaining study documentation while ensuring patient safety and

Qualificações

• University degree in medicine, science, or equivalent.
• MUST have previous onsite monitor experience (SIV, routine and close-out visits).
• Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data.
• Excellent written and verbal English communication.

Responsabilidades

• Coordinate all activities for setting up and monitoring a study, ensuring accurate status reports and proper study documentation.
• Run sponsor-generated queries efficiently and contribute to study cost efficiency; assist in preparation and review of study documentation and feasibility studies.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by adhering to ICON's procedures, protocols, and regulatory requirements.
• Fulll Service and Sponsor Dedicated roles.

Conhecimentos

Clinical trial monitoring

SIV / site visits

ICH-GCP

English communication

Formação académica

University degree in medicine or science

Descrição da oferta de emprego

CRA II and SR CRA - Remote - Brazil

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.

What You Will Do:

Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.
• Full Service and Sponsor Dedicates roles

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

• University degree in medicine, science, or equivalent
• MUST have previous experience as a monitor onsite (SIV, routine and close our visits)
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Excellent written and verbal communication in English