IQVIA (formerly Quintiles and IMS Health, Inc.) is seeking Clinical Leads to provide global study leadership. This role is responsible for ensuring the clinical delivery of assigned projects in compliance with regulatory requirements, including ICH-GCP, protocols, and internal policies. The successful candidate will manage clinical risks, project finances, recruitment strategies, and clinical teams to ensure high-quality project execution and milestone achievement.
Key Responsibilities
Compliance & Project Delivery: Ensure clinical delivery of projects meets ICH-GCP, protocol, customer, and internal requirements (SOPs, project plans).
Recruitment Management: Accountable for meeting project recruitment targets and ensuring appropriate strategies are implemented.
Risk & Quality Management: Contribute to the development of project risk mitigation plans, manage clinical risks, and monitor compliance with quality standards.
Financial Oversight: Manage project finances including Estimate at Completion (EAC); monitor changes against baseline and identify additional service opportunities or out-of-scope work.
Stakeholder Management: Identify and manage internal and external stakeholder landscapes through effective communication and resolution management.
Team Leadership: Handle resourcing and talent planning; establish operational plans, guidance, and project-related training for the clinical team.
Professional Development: Support the clinical team's development by providing performance feedback to line managers and mentoring new peers.
Business Support: Contribute to clinical delivery strategies for proposals and participate in bid defense preparations and meetings.
Qualifications and Requirements
Education: Bachelor's Degree in health care or another scientific discipline is required.
Experience: At least 5 years of clinical research or monitoring experience (or equivalent combination of education and training).
Technical Knowledge: Basic knowledge of project management practices and terminology; strong understanding of ICH-GCP guidelines and applicable regulatory requirements.
Industry Insight: Broad protocol and therapeutic knowledge, with a good understanding of the clinical research industry (drug/device/technology).
Financial Acumen: Understanding of project finances and Estimate at Completion (EAC) processes.
Trial Conduct: Knowledge of clinical trial conduct, local laws, and regulations.
How to Apply
Interested and qualified candidates should apply online through the IQVIA careers portal by following this link: Apply Here
How to Apply
Interested and qualified candidates should apply online through the IQVIA career portal using the application link provided below.
