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.
DescriptionThe role will 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 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.
This position will be office based in our Durham, NC office.
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.
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.
• 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
• 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
EEO Minorities/Females/Protected Veterans/Disabled
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™.
A little about us:
IQVIA™ has approximately 55,000 employees in more than 100 countries, all committed to making the potential of Human Data Science a reality, and we are actively hiring.