Madrid, Spain | Full time | Home-based | R1550716
Overview
Customer dedicated Clinical Project Management Director taking an Indication Director role to provide operational delivery oversight for select indication(s). Provides strategic and operational leadership for indication-level delivery, translating strategy into effective execution from phase II to submission while ensuring clinical trials are delivered on time and to plan. The role aligns resource planning with program needs, supports cross-functional team leadership, and drives problem-solving, risk management, and decision-making across studies within the indication. Acting as a key liaison between IQVIA and customer, it ensures clear communication, accountability, and alignment to partnership goals, while fostering a high-performing, innovative team culture grounded in customers operating principles.
Focus on leveraging therapeutic expertise and IQVIA's suite of solutions to drive operational excellence and strategic leadership with our customers.
Competencies
Leadership & Influence: Ability to lead cross-functional teams, inspire collaboration, and drive performance.
Strategic Thinking: Skilled in translating high-level strategy into actionable operational plans.
Problem-Solving: Solution-oriented mindset with strong risk identification and mitigation skills.
Communication: Excellent verbal and written communication skills for stakeholder engagement and decision-making.
Change Management: Demonstrated ability to implement organizational principles and foster continuous improvement.
Cultural Alignment: Role models humility, co-creation, and excellence while empowering teams and promoting innovation.
Essential Functions
Qualifications
Industry experience in Biotech or BioPharma.
Proven track record in indication-level strategy and delivery within a CRO or pharmaceutical or biotech environment.
Bachelor's Degree Life sciences or related field
Minimum 12 years of industry, clinical research experience preferred, including significant operational leadership in global trials.
Requires extensive knowledge of multiple job areas obtained through advanced education and experience.
Viewed as a leading expert within the field by peers.
Strong understanding of clinical development processes, regulatory requirements, and GCP compliance.
Experience in resource forecasting and strategic planning for complex programs.
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.
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