Vaga de parceiro

CFSP Dedicated Line Manager - São Paulo / SP

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Detalhes da Vaga

  • Escolaridade Não Informado
  • Segmento Não Informado
  • Salário Não Informado
  • Área de AtuaçãoDiversos / Outros

O que você irá fazer

  • We are a leading company committed to excellence and innovation, seeking a talented Senior Recruiter to support our growth.
  • Job Overview: Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced, employees are trained, and project objectives are met.
  • Key Responsibilities: Manage staff in accordance with organizational policies and applicable regulations.
  • Responsibilities include planning, assigning, directing work, assessing performance, guiding professional development, rewarding and disciplining employees, and addressing employee relations issues.
  • Participate in hiring processes by reviewing candidates and conducting interviews.
  • Ensure proper onboarding and training for new employees.
  • Ensure staff have the necessary materials, system access, and training to perform their duties.
  • Oversee training plans, SOP reviews, and training experiences.
  • Allocate resources to clinical research projects by assigning staff based on their experience and training.
  • Review and evaluate the clinical work of staff regularly to ensure quality standards are met.
  • Identify quality risks and issues, and develop corrective actions to address deficiencies.
  • Monitor workload and quality metrics, reporting findings to clinical operations management.
  • Collaborate with other clinical teams and leadership to manage project challenges and improve customer service.
  • Participate in quality and process improvement initiatives within the organization.
  • Basic Qualifications: Bachelor''s Degree in a scientific discipline or healthcare preferred.
  • Previous clinical trial experience, including management or leadership roles, or an equivalent combination of education and experience.
  • Deep knowledge of clinical research regulatory requirements (e.
  • g.
  • , GCP, ICH guidelines).
  • Other Requirements: Strong attention to detail and excellent communication skills.
  • Effective leadership abilities.
  • Exceptional problem-solving, judgment, and decision-making skills.
  • Proficiency in Microsoft Word, Excel, PowerPoint, and familiarity with using laptops, iPhones, and iPads.
  • Good command of written and verbal English communication skills.
  • Organizational and problem-solving skills.
  • Time and financial management skills.
  • Ability to establish and maintain effective working relationships with colleagues, managers, and clients.
  • Why Join Us? Be part of an innovative, forward-thinking company dedicated to improving health worldwide.
  • Work with a diverse and talented team.
  • Opportunities for professional growth, especially in project management.
  • Competitive salary and benefits package.
  • IQVIA values diversity and inclusion, aiming to attract and retain top talent regardless of gender, race, ethnicity, age, disability, sexual orientation, gender identity, or other characteristics.
  • Join us! IQVIA is a global leader in clinical research services, healthcare insights, and medical solutions, committed to accelerating medical advancements and improving patient outcomes worldwide.
  • Learn more at .
  • #J-18808-Ljbffr

Informações Adicionais

  • Quantidade de Vagas 1
  • Jornada Não Informado
 

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