Assoc Dir, Clin Leads

Job Overview:

Provide oversight and leadership to Clinical Leads (CL) for project productivity, delivery and quality resulting in strong financial performance and customer satisfaction. Work with Clinical Lead (CL) teams to focus on leveraging deep therapeutic expertise and IQVIA solutions to drive operational excellence and strategic leadership with our customers.

Direct and manage an assigned team of clinical leads who lead or support studies or programs to make sure quality, time and budget deliverables are met to the Sponsor’s satisfaction and in accordance with Attract, develop and retain talent.

RESPONSABILITIES:

-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).

Ensure all Clinical Leads (CLs) obtain Fundamental Good Clinical Practices (GCP) accreditation during a two year cycle.

-Actively engage with Clinical Leads (CLs) to review project performance and deliverables.

-Address CL performance issues and/or escalations by working with Clinical Leads (CLs) to create action/recovery plans.

-Ensure compliance to the Clinical Leads (CL) metrics dashboard of all direct reports.

-Foster an environment where lessons learned are shared within the team.

-Ensure compliance on the overall Risk Management process including risks that are escalating into issues.

-Work with Clinical Leads (CLs) on identification of risks that can lead to processes improvement/standardization across the organization.

-Mentor Clinical Leads (CLs) to manage clinical aspects of Project Finances including Estimate at Completion (EAC). Support Clinical Leads (CLs) to understand the scope of clinical delivery and create plans to deliver against this scope and to monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.

REQUIREMENTS:

-Knowledge of clinical trials: in depth knowledge and skill in applying, applicable clinical research regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Strong understanding of the Clinical Research Industry and the relevant environments in which it operates.;

-People Management : Proven ability to manage a team and work alongside others in a global environment to deliver results whilst meeting quality and timeline metrics. Provides others with a clear direction, delegates work appropriately and fairly, motivates and empowers others, monitors/manages performance and provides feedback and coaching.

Work conditions:

100% home based

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.