Associate Clinical Lead

Iqvia; São Paulo; Presencial; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A leading healthcare consultancy in São Paulo is seeking an Associate Clinical Lead. This role involves ensuring regulatory compliance and meeting recruitment targets for clinical projects. Strong communication skills and a Bachelor's in health care or related field are required. The ideal candidate will have knowledge of GCP and ICH guidelines along with a solid understanding of the clinical research industry. This position plays a critical part in enhancing drug delivery to improve patients' lives.

Qualificações

• Bachelor's degree in health care or other scientific discipline required.
• Good knowledge of clinical research regulatory requirements.
• Understanding of the Clinical Research industry.

Responsabilidades

• Ensure clinical delivery of assigned projects in compliance with regulations.
• Accountable for meeting project recruitment targets.
• Contribute to the development of project risk mitigation plans.
• Ensure clinical quality delivery by identifying quality standards.
• Manage internal and external stakeholders effectively.

Conhecimentos

Strong written and verbal communication skills

Knowledge of GCP and ICH guidelines

Broad protocol knowledge

Understanding of Clinical Research industry

Formação académica

Bachelor's Degree in health care or scientific discipline

Descrição da oferta de emprego

Associate Clinical Leads are an integral part of clinical trial delivery, working alongside

clinical teams to improve patients' lives by bringing new drugs to the market faster.

The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices.

Associate Clinical Leads partner with Project Leaders and other functional teams to secure delivery requirements are always met.

• You will
• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).
• Accountable for meeting projects' recruitment targets and ensuring appropriate recruitment strategies are in place.
• Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project's lifecycle.
• Ensure clinical quality delivery by identifying quality standards / requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.
• Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.
• What do you need to have?
• Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required
• Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Requires broad protocol knowledge and therapeutic knowledge.
• Requires good understanding of Clinical Research industry (drug / device / technology / etc.) and the relevant environments in which it operates.
• Communication - Strong written and verbal communication skills including good command of English language.