CRA II or Senior CRA

Pharmaceutical Research Associates, Inc; Brasil; Presencial; BRL 90.000 - 120.000; Tempo integral

Resumo da oferta

A leading Clinical Research organization in Brazil is seeking a Clinical Research Associate to oversee and ensure the integrity of clinical trials. Responsibilities include monitoring compliance with regulations, managing investigative site staff, and conducting risk assessments. Ideal candidates should have an undergraduate degree in a related field and previous clinical trial experience. This role requires 50-80% travel and offers a competitive salary along with various benefits.

Serviços

Competitive salary

Work-life balance opportunities

Inclusive work environment

Qualificações

• At least 1 year of experience in clinical trials, particularly on-site monitoring.
• Health care professional licensure, e.g., registered nurse.
• Ability to travel 50-80%.

Responsabilidades

• Conduct onsite and remote monitoring activities per ICH-GCP guidelines.
• Ensure study participant safety and data integrity.
• Manage site staff to meet trial deliverables.

Conhecimentos

Clinical trial monitoring

Data analysis

Fluent English

Risk assessment

Formação académica

Undergraduate degree in clinical, science, or health-related field

Descrição da oferta de emprego

Overview

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Responsibilities

What you will be doing:

• Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, providing instructions to site personnel and study close out.
• Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations.
• Ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations and SOPs.
• Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables.
• Verifies proper management and accountability of Investigational Product (IP).
• Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate.
• Manages essential documents as required by local regulations and ICH-GCP guidelines before, during and after a clinical study; assists with resolution of investigational site/data queries.
• Performs key risk assessment and management responsibilities throughout the project, including key risk indicator and site health analysis, site process evaluation, and project escalation.
• Participates in audit preparation and follow-up activities as needed.
• Independently performs a variety of onsite and offsite monitoring visit types.
• Gathers and reviews information for assigned siteand identifies inconsistencies. With limitedguidance from project and functional management, assesses risk and escalatesas appropriate.
• Assists with non-complex adhoc, short-term assignmentin support of additional studies or departmental initiatives.
• May serve as preceptor, providing training to less experienced clinical team members.

Qualifications

• Undergraduate degree or international equivalent in clinical, science, or healthrelated field from an accredited institution; health care professional licensure, i.e., registered nurse
• Previous experience supporting clinical trials including solid on-site monitoring experiencein CROs or pharma companies.
• Travel is required 50-80%.
• All employees must read, write and speak fluent English and host country language

What ICON can offer you:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsAt ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodationsInterested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.