Clinical Research Associate II

myGwork - LGBTQ+ Business Community; São Paulo; Presencial; BRL 60.000 - 100.000; Tempo integral

Resumo da oferta

An established industry player in clinical research is seeking a Clinical Research Associate (CRA) to enhance their team in Brazil. This role emphasizes the importance of building strong relationships with clinical sites while ensuring the integrity of clinical trials, particularly in oncology. As a CRA, you will conduct site visits, manage regulatory documentation, and develop patient recruitment strategies. With a focus on career development and a supportive work environment, this opportunity offers a chance to make a significant impact in the field of clinical research while enjoying the benefits of a flexible work culture and a bonus incentive program. If you are passionate about advancing healthcare and thrive in a collaborative setting, this position is for you.

Serviços

Bonus Incentive Program

Career Development Opportunities

Flexible Work Culture

Qualificações

• Experience in clinical research with a focus on oncology trials.
• Strong communication skills and ethical work approach are essential.

Responsabilidades

• Conduct site visits and ensure compliance with study protocols.
• Build relationships with clinical sites and protect patient rights.

Conhecimentos

Clinical Research

Oncology Trials

Interpersonal Communication

Problem-Solving

Time Management

Ethical Work Approach

Formação académica

Bachelor's degree in Biological Science

Equivalent degree in Pharmacy or Health-related discipline

Ferramentas

Clinical Trial Management System (CTMS)

Electronic Document Management System (EDMS)

MS-Office (Excel, Word)

Descrição da oferta de emprego

In Parexel we are looking for experienced CRA to make onsite monitoring visits in Brazil.

Oncology experience is required.

Your time here

At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRAs are accountable for using their expertise to build and maintain the site relationship and ensure they're set up for success. As the clinical sites' sole point of contact, this includes addressing and resolving site issues and questions. You'll also manage site quality and delivery from site identification through to close-out.

As a CRA, Parexel will offer you world-class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas, and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home.

What you'll do

1. Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV), and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
2. Build relationships. Oversee the integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
3. Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
4. Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
5. Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy, and drug accountability.
6. Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.

More about you

On your first day, we'll expect you to have:

1. Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
2. Experience working in Oncology Trials.
3. Ability to perform all clinical monitoring activities independently.
4. Bachelor's or equivalent degree in biological science, pharmacy, or other health-related discipline.
5. Strong interpersonal, written, and verbal communication skills within a matrixed team.
6. Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
7. A client-focused approach to work and flexible attitude with respect to assignments/new learning.
8. The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios, and achieve project timelines while being able to apply your understanding of study protocol(s).
9. An honest and ethical work approach to promote the development of life-changing treatments for patients.
10. Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.

A little about us

Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe. As a member of our team, you'll get to know your coworkers on a personal level. Have a question? A clinical research leader, project team member, technology 'super user', or collaborator are a phone call away. Our clinical research teams meet regularly to have discussions in an open environment, allowing our team members to share their expertise and promote learning within the team. Management supports and encourages career growth through consistent performance discussions and evaluations. Whether your interest is to progress into a more senior level CRA role, into line management, Quality, Project Leadership, or a variety of other positions, Parexel prides itself on career opportunities for our employees.