CRA 1

IQVIA; São Paulo; On-site; BRL 120,000 - 180,000; Full time

Benefits offered by this job

Competitive salary and benefits

Job summary

IQVIA in São Paulo, Brazil is seeking a Senior Recruiter to support our growth and help shape talent strategy across our organization.

You will partner with hiring teams, manage end-to-end recruitment processes, screen and assess candidates, and help ensure a positive candidate experience while upholding compliance with regulatory guidelines.

Join IQVIA to contribute to a dynamic, global team and drive impactful hiring outcomes in a fast-paced environment.

Qualifications

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

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with scope of work and regulatory requirements (GCP/ICH).
• Drive and track subject recruitment plans to enhance project predictability.
• Administer protocol and training to sites and maintain regular communication to manage expectations and issues.
• Evaluate quality and integrity of site practices and escalate issues.
• Track regulatory submissions, approvals, recruitment, CRF completion, data queries and resolution; may support start-up.
• Maintain TMF and ISF documentation per GCP/ICH and local regulations.
• Create and maintain site management documentation, visit reports, follow-up letters and study documentation.
• Collaborate with study team members for project execution.

Skills

Excellent command of English

Attention to detail

Problem-solving

Time management

Communication skills

Organizational skills

Microsoft Word

Microsoft Excel

PowerPoint

Education

Bachelor's degree in a scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

São Paulo, Brazil

Full time

R1568010

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.

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 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.

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