Cra 1 PCD

IQVIA; São Paulo; Presencial; BRL 120 000 - 180 000; Tempo integral

Resumo da oferta

IQVIA in Brazil (Sao Paulo) is seeking a Senior Recruiter to support growth through site monitoring and study coordination. You will ensure regulatory compliance, manage recruitment plans, and train site staff to maintain data integrity and protocol adherence.

The role requires strong English communication, attention to detail, and collaboration with cross-functional teams to drive project success in a fast-paced environment.

Qualificações

• Bachelor’s Degree in scientific discipline or health care preferred.
• Excellent command of English (written/spoken).
• Basic knowledge of regulatory requirements (GCP/ICH).
• Good therapeutic and protocol knowledge from company training.

Responsabilidades

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope of work and regulatory requirements (GCP/ICH).
• Work with sites to adapt, drive and track recruitment plans to align with project needs.
• Administer protocol training to sites and maintain regular communication with sites.
• Evaluate quality of site practices for protocol conduct and regulatory adherence.
• Escalate quality issues as appropriate.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• May support start-up phase.
• Ensure site documents are filed in the TMF and ISF is maintained per regulatory needs.
• Create and maintain site management documentation and visit reports.
• Collaborate with study team for project execution support.

Conhecimentos

English proficiency

Attention to detail

Communication skills

Organizational skills

Problem-solving

Formação académica

Bachelor’s degree in scientific discipline or health care

Ferramentas

Microsoft Word

Excel

PowerPoint

Descrição da oferta de emprego

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.comIQVIA 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. . Vaga Exclusiva para Pessoa com deficiência (PCD)