CRA2

IQVIA; São Paulo; Presencial; BRL 20.000 - 80.000; Tempo integral

Resumo da oferta

IQVIA is seeking a talented CRA 2 to support our growth in Brazil. As a CRA 2, you will perform monitoring and site management to ensure compliance with study protocols and regulatory requirements. Join our innovative team and enhance your project management skills through diverse professional growth opportunities. We offer a competitive salary and benefits package, fostering a diverse and inclusive work environment.

Serviços

Professional growth opportunities

Competitive salary and benefits package

Qualificações

• Bachelor's Degree in a scientific discipline or health care preferred.
• Excellent command of English (written/spoken).
• Basic knowledge of GCP and ICH guidelines.

Responsabilidades

• Perform site monitoring visits according to GCP and ICH guidelines.
• Manage the progress of assigned studies and track regulatory submissions.
• Evaluate quality and integrity of study site practices.

Conhecimentos

Attention to detail

Communication

Problem-solving

Formação académica

Bachelor's Degree in scientific discipline or healthcare

Ferramentas

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

iPhone and iPad

Descrição da oferta de emprego

Location: Brazil (Sao Paulo, Porto Alegre e Brasilia)

About Us: Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation, seeking a talented CRA 2 to support our growth.

Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Key Responsibilities:

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.

Basic Qualifications:

• Bachelor's Degree Degree in scientific discipline or health care preferred.
• Excellent command of English (written/spoken).
• Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
• Good therapeutic and protocol knowledge as provided in company training.

Others requirements:

• Strong attention to detail and excellent communication skills.
• Exceptional problem-solving, judgment, and decision-making abilities.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Why Join Us?

• Be part of an innovative and forward-thinking company that collaborates to make a healthier world.
• Work alongside a diverse and talented team.
• Many opportunities for professional growth by developing project mgmt abilities.
• Competitive salary and benefits package.

IQVIA is committed to embracing a diverse and inclusive work environment. Our goal is to attract and retain the best people, regardless of their gender, race, marital status, ethnic origin, national origin, age, disability, sexual orientation, gender identity or any other characteristic. Join us!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com