ACUTA
Providing Regulatory Information Management (RIM) solutions and services to the Life Sciences and related industry.
- Open roles
- 40
- New role every
- ~0.1 days
Company signals
Score: 69Job facts
- Location
- São Paulo, Brazil
- Type
- Full-time
- Posted
- May 22, 2026
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Clinical Lead (Oncology)
at ACUTA
Job Overview
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 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.
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.com
IQVIA 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.