Global Study Leadership - Assoc. Clinical Lead

Growth Troops; Buenos Aires; Presencial; ARS 86.914.000 - 115.887.000; Jornada completa

Descripción de la vacante

A global clinical research organization is seeking an Associate Clinical Lead to join their team in Buenos Aires. The role focuses on ensuring clinical delivery of projects, managing recruitment targets, and maintaining compliance with regulatory standards. Candidates should possess a Bachelor's Degree in health care and have strong communication skills in English. This position is essential for delivering projects successfully while enhancing patient care through clinical trials.

Formación

• Bachelor's Degree in health care or other scientific discipline.
• Good knowledge of applicable clinical research regulatory requirements.
• Strong written and verbal communication skills in English.

Responsabilidades

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements.
• Accountable for meeting projects’ recruitment targets.
• Contribute to the development of the project risk mitigation plan.

Conocimientos

Clinical research regulatory requirements

Clinical quality delivery

Communication skills

Protocol knowledge

Educación

Bachelor's Degree in health care or scientific discipline

Descripción del empleo

Global Study Leadership - Assoc. Clinical Lead

IQVIA

Job Overview

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 ensure 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 in health care or other scientific discipline.
• Good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Broad protocol knowledge and therapeutic knowledge.
• Good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.
• Strong written and verbal communication skills including good command of English language.

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