Project Management Analyst - Real-World Evidence Solutions en Madrid

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

PURPOSE

Manage, analyze and provide accurate and relevant data for Project Leaders to make informed decisions on strategies and
tactics to mitigate risk, control cost, and ensure customer satisfaction related to assigned project. The Project Management
Analyst (PMA) typically supports a project which is medium to large in scope and may also support a phase or portion of a large, complex project.

RESPONSIBILITIES

• • Establish and manage performance dashboards, analyze event triggers and alerts and determine appropriate follow up for Project Leader or others to act upon.
• Coordinate project schedules, estimates, cost control, risk management activities
• Review and approve project invoices on behalf of Project Leader or Project Integration Manager.
• Implement change order control processes.
• Ensure Project Leader has timely and accurate data on areas including cost, schedule, scope, utilization, change orders, quality to support better decision-making.
• Develop and maintain relevant sections of Project Execution Plans.
• Assist project sub-team leads in defining resource requirements, utilizes systems in order to monitor status.
• Prepare correspondence, including meeting minutes, for study team and/or customer
• Organize and support Project Leader in managing internal study team and customer meetings.
• Prepare presentation materials including study data for internal study team and customer meetings.
• Support study file review and audits as needed

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• •Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
• Strong written and verbal communication skills including good command of English language
• Results-oriented approach to work delivery and output
• Problem solving skills
• Planning, time management and prioritization skills
• Ability to handle conflicting priorities
• Attention to detail and accuracy in work
• Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Ability to work across cultures and geographies with a high awareness and understanding of cultural differences
• Ability to influence without authority

 MINIMUM REQUIRED EDUCATION AND EXPERIENCE

• •Bachelor's degree in life sciences or other related field and minimum of 1 year of relevant clinical research experience with analytical/financial skills; or equivalent combination of education, training and experience

PHYSICAL REQUIREMENTS

• •Extensive use of keyboard requiring repetitive motion of fingers.
• Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
• Regular sitting for extended periods of time.

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™