CRA II

ICON; Brasil; Teletrabalho; BRL 50.000 - 90.000; Tempo integral

Resumo da oferta

Join a forward-thinking company as a Clinical Research Associate, where you'll play a vital role in ensuring the integrity of clinical trials. This position offers a collaborative environment, allowing you to engage in both onsite and remote monitoring activities. You'll be responsible for verifying compliance with regulations, managing site staff, and ensuring participant safety. With a focus on professional growth, this role provides opportunities to develop your skills in a dynamic setting. If you're passionate about advancing healthcare through research, this is the perfect opportunity for you.

Serviços

Competitive Salary

Work-Life Balance Opportunities

Diverse Culture

Career Development Programs

Qualificações

• Experience in clinical trials and monitoring activities.
• Strong understanding of ICH-GCP guidelines and regulations.

Responsabilidades

• Conduct onsite and remote monitoring activities for clinical trials.
• Ensure compliance with protocols and protect study participants.

Conhecimentos

Clinical Trials Support

On-site Monitoring

Regulatory Compliance

Risk Assessment

Data Integrity

Formação académica

Undergraduate Degree in Clinical or Health-related Field

Health Care Professional Licensure

Descrição da oferta de emprego

A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity.

You will be joining a program takes an extensive co-monitoring approach that enables a supportive and collaborative work environment. Frequent, consistent communication, both internally and with our client, positions our program to be closely aligned on our shared goals.

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.

You are:

• 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 experience.
• Travel is required 50-80%.
• Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above. 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/benefits

At 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, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

https://careers.iconplc.com/reasonable-accommodations

Interested 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.