CRA 1

BZL IQVIA RDS Brasil Ltda; São Paulo; On-site; BRL 120,000 - 180,000; Full time

Job summary

IQVIA Inc in Sao Paulo, Brazil, is seeking a Senior Recruiter to support growth and drive excellence across clinical studies. The role emphasizes site monitoring coordination, regulatory adherence, and effective communication with study sites to ensure data integrity and study success.

Responsibilities include overseeing site visits, recruitment planning, regulatory tracking, and maintaining essential trial documentation in line with GCP and ICH guidelines.

Qualifications

• Bachelor's Degree required.
• Science or health care background preferred.
• Excellent command of English (written/spoken).
• Knowledge of GCP/ICH guidelines is a plus.

Responsibilities

• Perform site monitoring visits and manage site communications in line with protocol and regulatory requirements.
• Track regulatory submissions, recruitment, enrollment, and data queries for assigned studies.
• Create documentation of site management activities and maintain TMF/ISF in compliance with regulations.

Skills

English (Excellent)

Communication

Problem solving

Organization

Education

Bachelor's Degree

Science/Health care background preferred

Tools

MS Word

Excel

PowerPoint

Job description

Location: Brazil (Sao Paulo)

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 Senior Recruiter 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.
• 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 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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.