Cra 2 Pcd

Iqvia; São Paulo; On-site; BRL 90,000 - 150,000; Full time

Job summary

IQVIA in Sao Paulo, Brazil is seeking a Senior Recruiter to support growth while ensuring robust site monitoring activities in line with GCP and ICH guidelines. You will collaborate with sites to drive subject recruitment plans, administer training, and maintain high-quality study documentation throughout the TMF lifecycle.

The role requires strong attention to detail, excellent communication skills, and experience with regulatory requirements in clinical research.

Qualifications

• Bachelor 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 (GCP/ICH).
• Good therapeutic and protocol knowledge as provided in company training.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements.
• Drive and track subject recruitment plan to enhance predictability.
• Administer protocol and related study training to assigned sites and maintain regular communication with sites.
• Evaluate the quality and integrity of study site practices related to the protocol and regulations.
• Escalate quality issues as appropriate.
• Track regulatory submissions and approvals, recruitment and enrollment, CRF completion and data query resolution.

Skills

English proficiency

Education

Bachelor's Degree in Life Sciences

Tools

MS Word

MS 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.

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)