CRA1

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

Resumo da oferta

Join a leading global provider of clinical research services as a Site Manager. You will perform site monitoring and management to ensure compliance with study protocols and regulatory guidelines. This role offers opportunities for professional growth in an innovative and collaborative environment, alongside a talented team.

Serviços

Competitive salary and benefits package

Professional growth opportunities

Qualificações

• Excellent command of English (written/spoken) required.
• Basic knowledge of GCP and ICH guidelines.
• Good therapeutic and protocol knowledge as provided in company training.

Responsabilidades

• Conduct site monitoring visits including selection, initiation, and close-out.
• Evaluate study site practices for compliance with protocols and conduct.
• Manage project timelines including regulatory submissions and site documentation.

Conhecimentos

Attention to detail

Communication skills

Problem-solving

Organizational skills

Formação académica

Bachelor's Degree in scientific discipline or health care

Ferramentas

Microsoft Word

Excel

PowerPoint

Descrição da oferta de emprego

About Us: Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation.

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

About the company

IMS Health and Quintiles are now IQVIA. We are committed to providing solutions that enable healthcare companies to innovate with confidence, maximize opportunities and, ultimately, drive healthcare forward. We do this via breakthroughs in insights, t...

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