CRA 1

IQVIA; São Paulo; Presencial; BRL 60.000 - 100.000; Tempo integral

Resumo da oferta

Uma empresa inovadora e em crescimento está em busca de um Recrutador Sênior para ajudar a moldar o futuro da organização. Neste papel, você será responsável por monitorar e gerenciar sites de estudo, garantindo que as práticas estejam em conformidade com as diretrizes e regulamentos aplicáveis. Com um foco em recrutamento e comunicação eficaz, você terá a oportunidade de colaborar com uma equipe diversificada e talentosa, contribuindo para um mundo mais saudável. Se você é detalhista, possui habilidades excepcionais de comunicação e está pronto para enfrentar desafios, esta é a oportunidade ideal para você.

Serviços

Pacote de benefícios competitivo

Oportunidades de crescimento profissional

Trabalho em equipe diversificada

Qualificações

• Bacharelado em disciplina científica ou saúde é preferido.
• Excelentes habilidades de comunicação em inglês, escritas e faladas.

Responsabilidades

• Realizar visitas de monitoramento do site para garantir conformidade com o protocolo.
• Gerenciar o progresso dos estudos atribuídos, rastreando aprovações regulatórias.

Conhecimentos

Atenção aos detalhes

Comunicação

Resolução de problemas

Gestão do tempo

Gestão financeira

Formação académica

Bacharelado em disciplina científica ou saúde

Ferramentas

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

iPhone

iPad

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:

1. 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.
2. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
3. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
4. 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.
5. 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.
6. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
7. 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.
8. Collaborate and liaise with study team members for project execution support as appropriate.

Basic Qualifications:

1. Bachelor's Degree in scientific discipline or health care preferred.
2. Excellent command of English (written/spoken).
3. 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).
4. Good therapeutic and protocol knowledge as provided in company training.

Others requirements:

1. Strong attention to detail and excellent communication skills.
2. Exceptional problem-solving, judgment, and decision-making abilities.
3. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
4. Written and verbal communication skills including good command of English language.
5. Organizational and problem-solving skills.
6. Effective time and financial management skills.
7. Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Why Join Us?

1. Be part of an innovative and forward-thinking company that collaborates to make a healthier world.
2. Work alongside a diverse and talented team.
3. Many opportunities for professional growth by developing project management abilities.
4. Competitive salary and benefits package.