Sr. Director, Clinical Leads
IQVIA
Athens, Greece
πριν από 1 μέρα

Have you ever dreamt to be part of the strategic management of a company?

This could be your opportunity.

IQVIA is looking for a Senior Director Clinical Leads; a top management role which will allow you to be part of the future of one of the biggest company in the world.

Or maybe to write this future with your own hand.

If you have an outstanding clinical experience, a proven background of people and project management and you achieved great business goals, we are looking forward to connecting with you

Job Overview :

Provide senior oversight to Clinical Lead Teams for project productivity, delivery and quality resulting in strong financial performance and customer satisfaction.

Work with 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 Lead managers and Clinical Leads who lead teams or support studies or programs to make sure quality, time and budget deliverables are met to the Sponsor’s satisfaction and in accordance with Standard Operating Procedures (SOPs), policies and practices.

Ensure employees are trained and individual development is aligned and in place to meet project and organizational needs.

Main Duties :

Manage staff, planning, assigning, and directing work, appraising performance and guiding professional development, rewarding and disciplining employees, addressing employee relations issues and resolving problems.

Work with individual staff to make sure all study management and project deliverables are completed as contracted, to achieve quality deliverables on time and within budget and in accordance with Standard Operating Procedures (SOPs), policies and practices.

Coach and mentor employees around project planning, project review, risk management and problem solving to ensure global alignment of work practices across the team through the adoption and use of all process and technology tools and improvements by employees.

Obtain and provide regular feedback to employees from other project team members and key stakeholders to assist in personal and professional development.

Ensure direct reports demonstrate working knowledge of (Estimate at Completion) EAC, baseline and change control in terms of scope, budget, schedule and risk / issue management.

Complete and discuss the Clinical Lead competency framework with each direct report.

Actively engage with the review of project performance dashboard for tracked information. Follow up with direct reports to ensure system and metrics compliance.

Proactively manage risks linked to resourcing, project and / or individual needs with other management and leadership team members to manage study issues and obstacles.

Provide technical expertise and / or clinical project management experience to assigned staff for training and process improvement efforts.

Lead and / or actively participate in corporate initiatives, act as a departmental cross-functional liaison and / or change agent, provide technical expertise and clinical experience.

Act as a Clinical liaison with other groups within IQVIA.

Qualifications :

Strong academic background.

15 years of Clinical Experience and at least 8 years in a leadership capacity, working across several region and with a world-wide focus.

Broad management knowledge to lead cross-regional teams.

Deep knowledge of clinical trials.

Results Oriented.

Strong ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, Innovation, Ownership).

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 .

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